McKee's Pathology of the Skin
Kaup valmöguleikar
For trusted, comprehensive, and lavishly illustrated information on dermatopathology, look no further than McKee's Pathology of the Skin, 6th Edition. This fully revised reference provides clinical guidance from internationally renowned experts along with details on etiology, pathogenesis, histopathology, and differential diagnosis—making this unique resource unparalleled in its wealth of clinical and histopathological material.
It’s a must-have resource for practicing dermatopathologists and general pathologists who sign out skin biopsies.Covers pathological aspects of skin diseases in addition to providing superb descriptions and illustrations of their clinical manifestations—the only available reference with this unique combination of features.Offers highly illustrated coverage of inflammatory skin diseases, neoplastic conditions, infectious diseases, and other dermatological disorders, with sections on clinical correlations, histopathological features, and differential diagnoses, making it a valuable resource for both dermatologists and pathologists.Contains more than 5,000 superb histopathologic and clinical illustrations that demonstrate the range of histologic manifestations, and features bulleted lists of clinical features and differential diagnosis tables for easy reference.Brings you up to date with key molecular aspects of disease, including targeted therapy and personalized medicine.Includes an extensively revised chapter on melanoma that reflects recent significant changes in cancer research, the molecular mechanism of cancer, and the implications of these mechanisms in developing targeted therapies for treatment.Discusses key topics such as including the use of biologics for the treatment of inflammatory disease; new antigens/antibodies for tumor diagnosis and staging; next-generation sequencing and other molecular assays; improved clinical-pathological correlations for integrated care; increased understanding of genetic skin disorders and rare dermatological conditions; and much more.Any additional digital ancillary content may publish up to 6 weeks following the publication date.
Nánar um bókina
- Elsevier Limited (UK)
- 9780443381720
- 9780443113482
- ePub
- 6
- Eduardo Calonje
- English
- 2025-03-11
- 10
- 2
- 2
Kaflar
- Title of Book
- Cover image
- Title page
- Table of Contents
- Copyright
- Preface
- List of Contributors
- Acknowledgement
- Dedication
- Glossary of Abbreviations
- Volume One
- Chapter 1. The structure and function of skin
- Introduction
- Properties of skin
- Normal epidermal histology
- Regional variations in skin anatomy
- Skin development
- Keratinocyte biology
- Epidermal stem cells
- Skin barrier
- Skin immunity
- Melanocytes
- Merkel cells
- Intercellular junctions
- Pilosebaceous units
- Eccrine glands
- Apocrine glands
- Dermal-epidermal junction
- Dermal collagen
- Dermal elastic tissue
- Ground substance
- Fibroblast biology
- Cutaneous blood vessels and lymphatics
- Nervous system of the skin
- Subcutaneous fat
- Chapter 2. Specialized techniques in dermatopathology
- Specimen fixation, grossing, processing, embedding, and sectioning
- Routine and “special” stains
- Immunohistochemical techniques
- Immunohistochemical techniques and troubleshooting
- Immunofluorescence
- Electron microscopy
- Frozen section examination of skin specimens
- Diagnostic cytopathological techniques in dermatopathology
- Diagnosis of inherited skin diseases
- Molecular techniques
- Allelic imbalance
- Fluorescence in situ hybridization
- Comparative genomic hybridization
- Polymerase chain reaction
- Gene expression profiling
- Next-generation sequencing (NGS)
- Diagnosis of lymphomas
- Molecular analysis of cutaneous lymphoid infiltrates
- T-cell receptor gene rearrangement in cutaneous lymphoproliferation
- Immunoglobulin gene rearrangement in cutaneous lymphoproliferation
- Chapter 3. Disorders of keratinization
- Ichthyosis
- Ichthyosis vulgaris
- Clinical features
- Pathogenesis
- Histologic features
- Differential diagnosis
- X-linked (recessive) ichthyosis
- Clinical features
- Pathogenesis and histologic features
- Autosomal recessive congenital ichthyoses
- Genetics, pathogenesis, and phenotype
- Histologic features
- Harlequin ichthyosis
- Clinical features
- Pathogenesis and histologic features
- Autosomal-dominant lamellar ichthyosis
- Clinical features
- Pathogenesis and histologic features
- Differential diagnosis
- Keratinopathic ichthyoses
- Differential diagnosis
- Epidermolytic ichthyosis
- Pathogenesis and histologic features
- Annular epidermolytic ichthyosis
- Superficial epidermolytic ichthyosis
- Clinical features
- Pathogenesis and histologic features
- Epidermolytic epidermal nevus
- Epidermolytic acanthoma
- Clinical features
- Pathogenesis and histologic features
- Differential diagnosis
- Incidental epidermolytic hyperkeratosis
- Ichthyosis Curth-Macklin
- Clinical features
- Pathogenesis and histologic features
- Congenital reticular ichthyosiform erythroderma
- Clinical features
- Pathogenesis and histologic features
- Differential diagnosis
- Comèl-Netherton syndrome
- Clinical features
- Pathogenesis and histologic features
- Differential diagnosis
- Peeling skin syndromes
- Clinical features
- Keratosis linearis-ichthyosis congenita-sclerosing keratoderma
- Clinical features
- Pathogenesis and histologic features
- Severe dermatitis, multiple allergies, and metabolic wasting syndrome
- Sjögren-Larsson syndrome
- Clinical features
- Pathogenesis and histologic features
- Multiple sulfatase deficiency
- Refsum syndrome
- Clinical features
- Pathogenesis and histologic features
- Dorfman-Chanarin syndrome
- Pathogenesis and histologic features
- Trichothiodystrophy
- Neu-Laxova syndrome
- Ichthyosis prematurity syndrome
- Other rare neuro-ichthyotic syndromes
- Conradi-Hünermann-Happle syndrome
- Clinical features
- Pathogenesis and histologic features
- Follicular ichthyosis
- Ichthyosis follicularis with alopecia and photophobia
- Clinical features
- Pathogenesis and histologic features
- Differential diagnosis
- Ichthyosis with hypotrichosis
- Neonatal ichthyosis-sclerosing cholangitis syndrome
- Acquired ichthyosis-like conditions
- Pityriasis rotunda
- Clinical features
- Histologic features
- Keratosis pilaris
- Clinical features
- Histologic features
- Keratosis pilaris atrophicans
- Clinical features
- Pathogenesis and histologic features
- Lichen spinulosus
- Clinical features
- Histologic features
- Differential diagnosis
- Phrynoderma
- Clinical features
- Histologic features
- Erythrokeratoderma
- Erythrokeratoderma variabilis
- Clinical features
- Pathogenesis and histologic features
- Progressive symmetrical erythrokeratoderma
- Keratitis-ichthyosis-deafness syndrome, hystrix-like ichthyosis with deafness, and porokeratotic adnexal ostial nevus
- Clinical features
- Pathogenesis and histologic features
- Acquired symmetrical acrokeratoderma
- Palmoplantar keratoderma
- Epidermolytic palmoplantar keratoderma
- Clinical features
- Pathogenesis and histologic features
- Diffuse nonepidermolytic palmoplantar keratoderma
- Clinical features
- Pathogenesis and histologic features
- Huriez syndrome
- Clinical features
- Pathogenesis and histologic features
- Vohwinkel syndrome
- Clinical features
- Pathogenesis and histologic features
- Loricrin keratoderma
- Clinical features
- Pathogenesis and histologic features
- Clouston syndrome
- Clinical features
- Pathogenesis and histologic features
- Olmsted syndrome
- Clinical features
- Pathogenesis and histologic features
- Papillon-Lefèvre syndrome
- Clinical features
- Pathogenesis and histologic features
- Howel-Evans syndrome
- Clinical features
- Pathogenesis and histologic features
- Schöpf-Schulz-Passarge syndrome
- Clinical features
- Pathogenesis and histologic features
- Striate palmoplantar keratoderma
- Clinical features
- Pathogenesis and histologic features
- Differential diagnosis
- Hereditary painful callosities
- Clinical features
- Naxos syndrome
- Clinical features
- Pathogenesis and histologic features
- Carvajal-Huerta syndrome
- Clinical features
- Pathogenesis and histologic features
- McGrath syndrome
- Clinical features
- Pathogenesis and histologic features
- Pachyonychia congenita
- Clinical features
- Pathogenesis and histologic features
- Differential diagnosis
- Richner-Hanhart syndrome
- Clinical features
- Pathogenesis and histologic features
- Keratosis punctata palmoplantaris type Buschke-Fischer-Brauer
- Clinical features
- Pathogenesis and histologic features
- Differential diagnosis
- Keratosis punctata of the palmar creases
- Clinical features
- Histologic features
- Cole disease
- Clinical features
- Pathogenesis and histologic features
- Differential diagnosis
- Spiny keratoderma
- Marginal papular acrokeratoderma
- Clinical features
- Histologic features
- Acquired palmoplantar keratoderma and malignancies
- Acquired keratodermas and others
- Transient aquagenic keratoderma
- Pathophysiology and histology
- Clavus and callus
- Keratolytic winter erythema
- Clinical features
- Pathogenesis and histologic features
- Circumscribed palmar or plantar hypokeratosis
- Clinical features
- Pathogenesis and histologic features
- Acrokeratosis verruciformis of Hopf
- Clinical features
- Pathogenesis and histologic features
- Flegel disease (hyperkeratosis lenticularis perstans)
- Clinical features
- Pathogenesis and histologic features
- Porokeratosis
- Clinical features
- Pathogenesis
- Histologic features
- Differential diagnosis
- Waxy keratosis of childhood
- Digitate hyperkeratosis
- Pathogenesis and histologic features
- Granular parakeratosis
- Clinical features
- Pathogenesis and histologic features
- Differential diagnosis
- Hyperkeratosis of the nipple and areola
- Chapter 4. Inherited and autoimmune subepidermal blistering diseases
- Split skin immunofluorescence
- Immunoperoxidase antigen mapping
- Epidermolysis bullosa
- Bullous pemphigoid
- Pemphigoid gestationis
- Lichen planus pemphigoides
- Mucous membrane pemphigoid
- Epidermolysis bullosa acquisita
- Bullous systemic lupus erythematosus
- Dermatitis herpetiformis
- Linear IgA disease
- Chapter 5. Acantholytic disorders
- Introduction
- Pemphigus
- Pemphigus vulgaris
- Clinical features
- Pathogenesis and histologic features
- Endemic pemphigus vulgaris
- Differential diagnosis
- Pemphigus vegetans
- Clinical features
- Pathogenesis and histologic features
- Differential diagnosis
- Pemphigus foliaceus
- Clinical features
- Pathogenesis and histologic features
- Differential diagnosis
- Endemic pemphigus foliaceus (fogo selvagem)
- Clinical features
- Pathogenesis and histologic features
- Differential diagnosis
- Pemphigus herpetiformis
- Clinical features
- Pathogenesis and histologic features
- Differential diagnosis
- Pemphigus erythematosus
- Clinical features
- Pathogenesis and histologic features
- Differential diagnosis
- Paraneoplastic pemphigus (paraneoplastic autoimmune multiorgan syndrome)
- Clinical features
- Pathogenesis and histologic features
- Differential diagnosis
- IgA pemphigus
- Clinical features
- Pathogenesis and histologic features
- Differential diagnosis
- Drug-induced pemphigus
- Contact pemphigus
- Clinical features
- Pathogenesis and histologic features
- Differential diagnosis
- Acantholytic dermatoses with dyskeratosis
- Hailey–Hailey disease
- Clinical features
- Pathogenesis and histologic features
- Differential diagnosis
- Relapsing linear acantholytic dermatosis
- Clinical features
- Histologic features
- Darier disease
- Clinical features
- Pathogenesis and histologic features
- Differential diagnosis
- Linear Darier disease
- Clinical features
- Pathogenesis and histologic features
- Differential diagnosis
- Transient acantholytic dermatosis (Grover disease)
- Clinical features
- Pathogenesis and histologic features
- Differential diagnosis
- Acantholytic dermatosis of the genitocrural area
- Clinical features
- Pathogenesis and histologic features
- Warty dyskeratoma
- Clinical features
- Pathogenesis and histologic features
- Differential diagnosis
- Familial dyskeratotic comedones
- Clinical features
- Histologic features
- Differential diagnosis
- Acantholytic acanthoma
- Clinical features
- Pathogenesis and histologic features
- Differential diagnosis
- Acantholytic dyskeratotic acanthoma
- Clinical features
- Pathogenesis and histologic features
- Differential diagnosis
- Focal acantholytic dyskeratosis
- Clinical features
- Pathogenesis and histologic features
- Chapter 6. Spongiotic, psoriasiform, and pustular dermatoses
- Eczematous dermatitis
- Eczema: general considerations
- Endogenous dermatitis
- Atopic dermatitis
- Seborrheic dermatitis
- Discoid dermatitis (nummular eczema)
- Hand eczema (dyshidrotic eczema, palmoplantar eczema, pompholyx)
- Autosensitization (Id) reaction
- Exogenous dermatitis
- Contact dermatitis
- Infective dermatitis
- Asteatotic dermatitis
- Lichen simplex chronicus
- Nodular prurigo (prurigo nodularis) and prurigo nodule (picker nodule)
- Stasis dermatitis and acroangiodermatitis
- Pityriasis alba
- Actinic prurigo
- Papuloerythroderma (of Ofuji)
- Eosinophilic spongiosis
- Erythroderma
- Sulzberger-Garbe syndrome
- Vein graft site dermatitis
- Papular acrodermatitis of childhood
- Pityriasis rosea
- Juvenile plantar dermatosis
- Miliaria
- Fox-Fordyce disease
- Transient acantholytic dermatosis with prominent eccrine ductal involvement
- Psoriasiform dermatoses
- Psoriasis
- Reactive arthritis
- Pityriasis rubra pilaris
- Inflammatory linear verrucous epidermal nevus
- Bazex syndrome (acrokeratosis paraneoplastica)
- Pustular dermatoses
- Pustular drug reactions
- Subcorneal pustular dermatosis
- Toxic erythema of the neonate
- Infantile acropustulosis
- Transient neonatal pustular melanosis
- Erythema toxicum neonatorum
- Chapter 7. Lichenoid and interface dermatitis
- Lichenoid dermatoses
- Lichen planus
- Clinical features
- Pathogenesis and histologic features
- Differential diagnosis
- Lichen nitidus
- Clinical features
- Histologic features
- Differential diagnosis
- Lichenoid keratosis
- Clinical features
- Pathogenesis and histologic features
- Differential diagnosis
- Lichen striatus
- Clinical features
- Pathogenesis and histologic features
- Differential diagnosis
- Adult blaschkitis
- Clinical features
- Pathogenesis and histologic features
- Differential diagnosis
- Keratosis lichenoides chronica
- Clinical features
- Pathogenesis and histologic features
- Differential diagnosis
- Idiopathic eruptive macular pigmentation including erythema dyschromicum perstans, ashy dermatosis, and lichen planus pigmentosus
- Clinical features
- Pathogenesis and histologic features
- Differential diagnosis
- Lichenoid and granulomatous dermatitis
- Clinical features
- Pathogenesis and histology
- Differential diagnosis
- Annular lichenoid dermatitis (of youth)
- Clinical features
- Pathogenesis and histologic features
- Differential diagnosis
- Interface dermatoses
- Definitions
- Erythema multiforme
- Clinical features
- Pathogenesis and histologic features
- Differential diagnosis
- Toxic epidermal necrolysis and Stevens-Johnson syndrome
- Clinical features
- Pathogenesis and histologic features
- Differential diagnosis
- Paraneoplastic pemphigus
- Poikiloderma
- Poikiloderma of Civatte
- Histologic features
- Mitochondrial DNA syndrome–associated poikiloderma
- Rothmund-Thomson syndrome
- Clinical features
- Pathogenesis and histologic features
- Bloom syndrome
- Clinical features
- Pathogenesis and histologic features
- Differential diagnosis
- Cockayne syndrome
- Clinical features
- Pathogenesis and histologic features
- Dyskeratosis congenita
- Clinical features
- Pathogenesis and histologic features
- Graft-versus-host disease
- Clinical features
- Pathogenesis and histologic features
- Differential diagnosis
- Pityriasis lichenoides
- Clinical features
- Pathogenesis and histologic features
- Differential diagnosis
- Chapter 8. Superficial and deep perivascular inflammatory dermatoses
- Chronic superficial dermatitis
- Annular/gyrate erythema
- Erythema annulare centrifugum
- Clinical features
- Histologic features
- Differential diagnosis
- Erythema gyratum repens
- Clinical features
- Pathogenesis and histologic features
- Differential diagnosis
- Lymphocytic infiltrate of the skin (Jessner)
- Clinical features
- Pathogenesis and histologic features
- Differential diagnosis
- Reticular erythematous mucinosis
- Clinical features
- Pathogenesis and histologic features
- Differential diagnosis
- Polymorphous light eruption (including juvenile spring eruption and lambing ears)
- Clinical features
- Pathogenesis and histologic features
- Differential diagnosis
- Tumid lupus erythematosus
- Clinical features
- Histologic features
- Differential diagnosis
- Perniosis, atypical chilblains, and cold equestrian panniculitis
- Clinical features
- Pathogenesis and histologic features
- Differential diagnosis
- Chilblain lupus erythematosus
- Clinical features
- Pathogenesis and histologic features
- Differential diagnosis
- Pigmented purpuric dermatoses including Majocchi disease, Schamberg disease, pigmented purpuric lichenoid dermatitis of Gougerot and Blum, and itching purpura
- Clinical features
- Histologic features
- Differential diagnosis
- Lichen aureus
- Clinical features
- Histologic features
- Differential diagnosis
- Pruritic urticarial papules and plaques of pregnancy
- Clinical features
- Histologic features
- Differential diagnosis
- Pregnancy prurigo
- Clinical features
- Pathogenesis and histologic features
- Differential diagnosis
- Tumor necrosis factor receptor-associated periodic syndrome (familiar Hibernian fever)
- Clinical features
- Pathogenesis and histologic features
- Eosinophilic, polymorphic, and pruritic eruption associated with radiotherapy
- Clinical features
- Pathogenesis and histologic features
- Viral exanthemata
- Chapter 9. Granulomatous, necrobiotic, and perforating dermatoses
- Sarcoidosis
- Granuloma annulare
- Necrobiosis lipoidica
- Rheumatoid nodule
- Elastolytic granulomata
- Annular elastolytic giant cell granuloma (annular elastolytic granuloma)
- Clinical features
- Pathogenesis and histologic features
- Differential diagnosis
- Actinic granuloma (O’Brien)
- Clinical features
- Pathogenesis and histologic features
- Differential diagnosis
- Atypical facial necrobiosis lipoidica
- Clinical features
- Histologic features
- Differential diagnosis
- Granuloma multiforme
- Clinical features
- Histologic features
- Differential diagnosis
- Rheumatic fever nodule
- Clinical features
- Histologic features
- Differential diagnosis
- Necrobiotic xanthogranuloma
- Clinical features
- Pathogenesis and histologic features
- Differential diagnosis
- Palisaded neutrophilic and granulomatous dermatitis (Reactive granulomatous dermatitis)
- Clinical features
- Pathogenesis and histologic features
- Differential diagnosis
- ‘Metastatic’ Crohn disease
- Clinical features
- Pathogenesis and histologic features
- Differential diagnosis
- Granulomatous cheilitis
- Acne agminata
- Clinical features
- Pathogenesis and histologic features
- Differential diagnosis
- Periorificial (perioral) dermatitis
- Clinical features
- Pathogenesis and histologic features
- Demodicosis
- Pathogenesis and histologic features
- Infective granulomata
- Foreign body granulomata
- Granulomatous contact dermatitis
- Clinical features
- Pathogenesis and histologic features
- Differential diagnosis
- Granulomata in congenital immunodeficiency syndromes
- Perforating disorders
- Reactive perforating collagenosis
- Clinical features
- Pathogenesis and histologic features
- Differential diagnosis
- Perforating folliculitis
- Clinical features
- Pathogenesis and histologic features
- Differential diagnosis
- Elastosis perforans serpiginosa
- Clinical features
- Pathogenesis and histologic features
- Differential diagnosis
- Hyperkeratosis follicularis et parafollicularis in cutem penetrans (Kyrle disease)
- Clinical features
- Pathogenesis and histologic features
- Differential diagnosis
- Perforating pseudoxanthoma elasticum
- Necrotizing infundibular crystalline folliculitis
- Clinical features
- Pathogenesis and histologic features
- Chondrodermatitis nodularis chronica helicis
- Clinical features
- Pathogenesis and histologic features
- Differential diagnosis
- Chapter 10. Inflammatory diseases of the subcutaneous fat
- Introduction
- Erythema nodosum
- Erythema nodosum-like lesions in Behçet disease
- Weber–Christian disease
- α1-Antitrypsin deficiency-associated panniculitis
- Clinical features
- Pathogenesis and histologic features
- Differential diagnosis
- Factitial and traumatic panniculitis
- Clinical features
- Pathogenesis and histologic features
- Cold panniculitis
- Clinical features
- Histologic features
- Cytophagic histiocytic panniculitis
- Clinical features
- Pathogenesis and histologic features
- Differential diagnosis
- Subcutaneous Whipple disease
- Clinical features
- Histologic features
- Pancreatic panniculitis
- Clinical features
- Pathogenesis and histologic features
- Differential diagnosis
- Subcutaneous fat necrosis of the newborn
- Clinical features
- Pathogenesis and histologic features
- Differential diagnosis
- Sclerema neonatorum
- Clinical features
- Pathogenesis and histologic features
- Cutaneous oxalosis
- Clinical features
- Histologic features
- Calciphylaxis
- Clinical features
- Pathogenesis and histologic features
- Differential diagnosis
- Gouty panniculitis
- Clinical features
- Histologic features
- Nodular vasculitis
- Clinical features
- Pathogenesis and histologic features
- Differential diagnosis
- Subcutaneous sarcoidosis
- Clinical features
- Histologic features
- Differential diagnosis
- Neutrophilic lobular panniculitis associated with rheumatoid arthritis
- Clinical features
- Pathogenesis and histologic features
- Differential diagnosis
- Eosinophilic panniculitis
- Clinical features
- Histologic features
- Infective panniculitis
- Clinical features
- Histologic features
- Acute infectious id panniculitis—panniculitic bacterid
- Clinical features
- Histologic features
- Differential diagnosis
- Sclerosing panniculitis
- Clinical features
- Pathogenesis and histologic features
- Differential diagnosis
- Membranous fat necrosis
- Clinical features
- Pathogenesis and histologic features
- Lipodystrophies
- Familial lipodystrophy
- Congenital generalized lipodystrophy (Berardinelli–Seip syndrome)
- Familial partial lipodystrophy syndromes
- Familial partial lipodystrophy (Köbberling syndrome, FPLD type 1)
- Familial partial lipodystrophy (Dunnigan disease, FPLD type 2)
- Familial partial lipodystrophy associated with mandibuloacral dysplasia
- Acquired lipodystrophy
- Acquired generalized lipodystrophy
- Acquired partial lipodystrophy
- Localized lipoatrophy
- Lipoatrophic panniculitis
- Lipophagic panniculitis of childhood
- Connective tissue panniculitis
- Lupus erythematosus profundus
- Scleroderma panniculitis
- Dermatomyositis panniculitis
- Postirradiation pseudosclerodermatous panniculitis
- Chapter Chapter 11. Histopathology of factitious skin lesions
- Introduction
- Factitious lesions caused by mechanical injury
- Continuous, persistent
- Isolated, occasional
- Factitious lesions caused by thermal or electrical injury
- Burns
- Delayed reactions to thermal injury
- Factitious lesions caused by chemical/biological injury
- Injury through external application
- Injury through injection
- Chapter 12. Diseases of the oral mucosa
- Introduction
- Hereditary Conditions
- Macular lesions
- White sponge nevus (Canon white sponge nevus)
- Hereditary benign intraepithelial dyskeratosis
- Pachyonychia congenita
- Dyskeratosis congenita
- Darier disease (Darier–White disease, keratosis follicularis)
- Tumor-like lesions
- Choristomas and heterotopias
- Heterotopic brain tissue (glial heterotopia)
- Oral lymphoepithelial cyst
- Epidermoid, dermoid, and teratoid cysts
- Congenital granular cell tumor/epulis
- Lingual thyroid
- Lymphangioma/lymphatic ectasia of the alveolar ridge in the newborn
- Gingival fibromatosis
- Hyaline fibromatosis (hyaline fibromatosis syndrome)
- Reactive Conditions
- Leukoedema
- Morsicatio mucosae oris/chronic frictional or factitial (bite) keratosis
- Benign alveolar ridge keratosis/oral lichen simplex chronicus
- Smokeless tobacco lesion (snuff dipper keratosis)/irritant contact stomatitis
- Benign migratory glossitis (geographic tongue, geographic stomatitis, stomatitis/erythema areata migrans)
- Foreign body gingivitis
- Warty dyskeratoma
- Nicotinic stomatitis (stomatitis nicotina)
- Ulcerative Conditions
- Recurrent aphthous stomatitis
- Traumatic ulcerative granuloma (traumatic ulcerative granuloma with stromal eosinophilia, eosinophilic ulcer/granuloma of the tongue, Riga–Fede disease)
- Pyostomatitis vegetans
- Papillary Lesions
- Squamous papilloma
- Verruciform xanthoma
- (Localized juvenile) spongiotic gingival hyperplasia
- Tumor-like Conditions
- Fibroma (fibrovascular polyp, fibroepithelial polyp)
- Giant cell fibroma
- Lipoma
- Denture-associated fibrous hyperplasia (inflammatory fibrous hyperplasia, epulis fissuratum, inflammatory papillary hyperplasia)
- Gingival nodules
- Gingival fibroma (inflammatory fibrous hyperplasia)
- Pyogenic granuloma/inflammatory fibrovascular hyperplasia or polyp
- Peripheral ossifying fibroma (fibrous hyperplasia with osseous metaplasia)
- Peripheral giant cell granuloma
- Parulis
- Gingival cyst of the adult
- Peripheral odontogenic fibroma
- Generalized gingival hyperplasia
- Varix and vascular malformation
- Infections
- Median rhomboid glossitis
- Hairy leukoplakia
- Focal epithelial hyperplasia (Heck disease, multifocal papillomavirus epithelial hyperplasia)
- Lichenoid and Hypersensitivity Reactions
- Oral lichen planus and lichenoid stomatitis
- Plasma cell gingivostomatitis
- Orofacial granulomatosis
- Oral Crohn disease
- Autoimmune Conditions
- Desquamative gingivitis
- Mucous membrane pemphigoid
- Pemphigus vulgaris
- Paraneoplastic pemphigus (paraneoplastic autoimmune multiorgan syndrome)
- Linear IgA disease
- Dermatitis herpetiformis
- Epidermolysis bullosa acquisita
- Lupus erythematosus
- Granulomatosis with polyangiitis (Wegener granulomatosis)
- Salivary Gland Disease
- Reactive conditions
- Mucocele and salivary duct cyst
- Sialolith
- Necrotizing sialometaplasia
- Cheilitis glandularis (stomatitis glandularis, cheilitis glandularis apostematosa)
- Salivary gland neoplasms
- Pleomorphic adenoma
- Canalicular adenoma
- Mucoepidermoid carcinoma
- Polymorphous adenocarcinoma
- Adenoid cystic carcinoma
- Papillary ductal lesions
- Precancerous Conditions
- Leukoplakia, erythroplakia, and epithelial dysplasia
- Submucous fibrosis
- Squamous Cell Carcinoma and Variants
- Squamous cell carcinoma
- Sarcomatoid squamous cell carcinoma (spindle cell carcinoma)
- Basaloid squamous cell carcinoma
- Adenoid (acantholytic, pseudoglandular, pseudovascular) squamous cell carcinoma
- Adenosquamous carcinoma
- Verrucous carcinoma and papillary squamous cell carcinoma
- Oral Lymphoma
- Pigmented Lesions
- Amalgam tattoo
- Oral melanocytic lesions
- Oral melanotic macule
- Melanoacanthosis
- Medication-induced oral pigmentation
- Oral melanocytic nevus
- Oral melanoma
- Other Tumors
- Granular cell tumor
- Ectomesenchymal chondromyxoid tumor
- Chapter 13. Diseases of the anogenital skin
- Introduction
- Embryology
- Normal female anatomy
- Labia majora and perianal skin
- Labia minora and clitoral prepuce
- Glans clitoris
- Vestibule
- Normal male anatomy
- Histologic features
- Pubic hair
- Anogenital mammary-like glands
- Normal variants
- Pigmentation
- Circumcision
- Acrochordons
- Clinical features
- Histologic features
- Pearly penile papules
- Clinical features
- Histologic features
- Vestibular papillomatosis
- Clinical features
- Histologic features
- Sebaceous gland hyperplasia
- Clinical features
- Histologic features
- Inflammatory dermatoses
- Intertrigo and balanoposthitis
- Clinical features
- Pathogenesis and histologic features
- Nonspecific balanoposthitis
- Eczema
- Clinical features
- Histologic features
- Seborrheic dermatitis
- Clinical features
- Infantile gluteal granuloma
- Clinical features
- Histologic features
- Differential diagnosis
- Lichen simplex
- Clinical features
- Histologic features
- Psoriasis
- Clinical features
- Histologic features
- Reactive arthritis
- Clinical features
- Histologic features
- Differential diagnosis
- Lichen planus
- Clinical features
- Pathogenesis and histologic features
- Differential diagnosis
- Lichen nitidus
- Clinical features
- Histologic features
- Porokeratosis
- Clinical features
- Histologic features
- Lichen sclerosus
- Clinical features
- Pathogenesis and histologic features
- Differential diagnosis
- Zoon balanitis
- Clinical features
- Pathogenesis and histologic features
- Zoon vulvitis (plasma cell vulvitis)
- Clinical features
- Histologic features
- Granuloma annulare
- Vesiculobullous conditions
- Genital papular acantholytic dyskeratosis
- Penile acne
- Clinical features
- Histologic features
- Vulval acne
- Hidradenitis suppurativa
- Clinical features
- Histologic features
- Aphthous ulceration
- Clinical features
- Histologic features
- Lipschutz ulcer (Reactive nonsexually acquired acute genital ulcers)
- Clinical features
- Pathogenesis and histologic features
- Sclerosing lymphangitis of the penis
- Clinical features
- Pathogenesis and histologic features
- Pyoderma gangrenosum
- Histologic features
- Penile necrosis
- Clinical features
- Histologic features
- Spontaneous scrotal ulceration
- Scrotal fat necrosis
- Associations with systemic disease
- Crohn disease
- Clinical features
- Histologic features
- Acute hemorrhagic edema of childhood
- Clinical features
- Pathogenesis and histologic features
- Behçet disease
- Necrotizing vasculitis
- Infectious diseases
- Erythrasma
- Clinical features
- Pathogenesis and histologic features
- Tinea
- Trichosporosis
- Clinical features
- Histologic features
- Condyloma acuminatum (genital warts, HPV infection)
- Clinical features
- Histologic features
- Syphilis
- Clinical features
- Pathogenesis and histologic features
- Granuloma inguinale
- Clinical features
- Pathogenesis and histologic features
- Chancroid
- Clinical features
- Pathogenesis and histologic features
- Lymphogranuloma venereum
- Clinical features
- Pathogenesis and histologic features
- Schistosomiasis
- Clinical features
- Pathogenesis and histologic features
- Amebiasis cutis
- Clinical features
- Histologic features
- Demodecidosis
- Malacoplakia
- Clinical features
- Pathogenesis and histologic features
- Fournier gangrene
- Miscellaneous conditions
- Vulvodynia
- Idiopathic calcinosis
- Clinical features
- Pathogenesis and histologic features
- Vulval elastosis
- Dermatitis artefacta
- Sclerosing lipogranuloma
- Clinical features
- Histologic features
- Pilonidal sinus
- Clinical features
- Histologic features
- Cyclist’s vulva
- Genital pigmented lesions
- Genital melanosis
- Clinical features
- Histologic features
- Genital melanocytic nevi
- Clinical features
- Pathogenesis and histologic features
- Melanoma
- Clinical features
- Pathogenesis and histologic features
- Benign epithelial lesions
- Localized epidermolytic hyperkeratosis/epidermolytic acanthoma
- Verruciform xanthoma
- Benign mucinous metaplasia and mucinous syringometaplasia
- Endometriosis and endosalpingiosis
- Clinical features
- Histologic features
- Median raphe cyst
- Clinical features
- Pathogenesis and histologic features
- Bartholin duct cyst
- Clinical features
- Histologic features
- Mucinous cyst
- Clinical features
- Pathogenesis and histologic features
- Mesonephric cyst
- Clinical features
- Histologic features
- Mesothelial cyst
- Clinical features
- Histologic features
- Periurethral cyst
- Clinical features
- Histologic features
- Penile horn
- Pseudoepitheliomatous, keratotic, and micaceous balanitis
- Clinical features
- Histologic features
- Genital intraepithelial neoplasia and squamous cell carcinoma
- Vulval intraepithelial neoplasia
- Clinical features
- Histologic features
- Squamous cell carcinoma of the female genital epithelia
- Verrucous carcinoma
- Clinical features
- Histologic features
- Penile intraepithelial neoplasia
- Histologic features
- Basaloid PeIN
- Warty (condylomatous) PeIN
- Penile invasive squamous cell carcinoma
- Subtypes of penile squamous cell carcinoma (WHO classification, 2022, Table 13.1)
- Clinical features
- Histologic features
- Pseudohyperplastic carcinoma
- Clinical features
- Histologic features
- Pseudoglandular (acantholytic, adenoid) carcinoma
- Clinical features
- Histologic features
- Verrucous carcinoma
- Clinical features
- Histologic features
- Carcinoma cuniculatum
- Clinical features
- Histologic features
- Papillary carcinoma, not otherwise specified
- Clinical features
- Histologic features
- Sarcomatoid carcinoma (carcinoma with heterologous differentiation, metaplastic carcinoma)
- Clinical features
- Histologic features
- Mixed carcinoma
- Clinical features
- Histologic features
- Clinical features
- Histologic features
- Condylomatous (warty) carcinoma
- Clinical features
- Histologic features
- Warty–basaloid carcinoma
- Clinical features
- Histologic features
- Clear cell carcinoma
- Clinical features
- Histologic features
- Lymphoepithelioma-like carcinoma
- Clinical features
- Histologic features
- Penile SCC not covered in any of the previous categories
- Clinical features
- Histologic features
- Squamous cell carcinoma, not otherwise specified (NOS)
- Other rare carcinomas
- Giant condyloma
- Cloacogenic carcinoma
- Tumors of anogenital mammary-like glands
- Papillary hidradenoma (hidradenoma papilliferum)
- Clinical features
- Pathogenesis and histologic features
- Fibroadenoma and phyllodes tumor
- Clinical features
- Pathogenesis and histologic features
- Benign tumors of Bartholin gland
- Clinical features
- Histologic features
- Adenoma of minor vestibular glands
- Clinical features
- Histologic features
- Bartholin gland carcinoma
- Clinical features
- Histologic features
- Other vulval adnexal neoplasms
- Basal cell carcinoma
- Clinical features
- Histologic features
- Metastatic tumors
- Lymphoma and leukemia
- Juvenile xanthogranuloma
- Langerhans cell histiocytosis
- Soft tissue tumors
- Keloid
- Fibroepithelial stromal polyp
- Clinical features
- Histologic features
- Differential diagnosis
- Lymphedematous fibroepithelial polyp of the glans penis and prepuce
- Clinical features
- Histologic features
- Prepubertal vulval fibroma
- Clinical features
- Histologic features
- Angiomyofibroblastoma
- Clinical features
- Pathogenesis and histologic features
- Differential diagnosis
- Deep (aggressive) angiomyxoma
- Clinical features
- Histologic features
- Differential diagnosis
- Cellular angiofibroma
- Clinical features
- Pathogenesis and histologic features
- Differential diagnosis
- Genital leiomyoma
- Clinical features
- Histologic features
- Vulvovaginal myxoid epithelioid tumor with smooth muscle differentiation
- Leiomyosarcoma
- Clinical features
- Histologic features
- Vulval leiomyomatosis
- Clinical features
- Pathogenesis and histologic features
- Myointimoma
- Clinical features
- Histologic features
- Differential diagnosis
- Postoperative spindle cell nodule
- Clinical features
- Pathogenesis and histologic features
- Chapter 14. Degenerative and metabolic diseases
- The hyperlipidemias
- Eruptive xanthomata
- Clinical features
- Histologic features
- Differential diagnosis
- Tendinous xanthomata
- Clinical features
- Histologic features
- Tuberous xanthomata
- Clinical features
- Histologic features
- Differential diagnosis
- Planar xanthomata
- Clinical features
- Histologic features
- Verruciform xanthoma
- Clinical features
- Pathogenesis and histologic features
- Differential diagnosis
- Angiokeratoma corporis diffusum
- Clinical features
- Pathogenesis and histologic features
- Differential diagnosis
- The amyloidoses
- Primary and myeloma-associated systemic amyloidoses
- Clinical features
- Histologic features
- Secondary amyloidosis
- Hemodialysis-associated amyloidosis
- Clinical features
- Histologic features
- 12-Heredofamilial amyloidoses
- Familial Mediterranean fever
- Pathogenesis and histologic features
- Familial amyloidotic polyneuropathy
- Histologic features
- Amyloid elastosis
- Clinical features
- Histologic features
- Primary localized cutaneous amyloidosis, lichen and macular types
- Clinical features
- Pathogenesis and histologic features
- Secondary localized cutaneous amyloidosis
- Familial primary cutaneous amyloidosis
- Nodular amyloidosis
- Clinical features
- Histologic features
- Colloid milium
- Juvenile colloid milium
- Clinical features
- Pathogenesis and histologic features
- Adult colloid milium
- Clinical features
- Pathogenesis and histologic features
- Hyalinosis cutis et mucosae
- Clinical features
- Pathogenesis and histologic features
- Cutaneous macroglobulinosis
- Clinical features
- Histologic features
- Porphyria
- Congenital erythropoietic porphyria
- Clinical features
- Erythropoietic protoporphyria
- Clinical features
- Hereditary coproporphyria
- Clinical features
- Porphyria cutanea tarda
- Clinical features
- Hepatoerythropoietic porphyria
- Clinical features
- Variegate porphyria
- Clinical features
- Histologic features of the porphyrias
- Differential diagnosis
- Pseudoporphyria
- Clinical features
- Pathogenesis and histologic features
- Differential diagnosis
- Gout
- Clinical features
- Histologic features
- Ochronosis
- Alkaptonuria
- Clinical features
- Exogenous ochronosis
- Clinical features
- Pathogenesis and histologic features
- Hartnup disease
- Clinical features
- Histologic features
- Pellagra
- Clinical features
- Histologic features
- Differential diagnosis
- Scurvy
- Clinical features
- Pathogenesis and histologic features
- Calcinosis cutis
- Dystrophic calcinosis cutis
- Clinical features
- Metastatic calcinosis cutis
- Clinical features
- Idiopathic calcinosis cutis
- Clinical features
- Pathogenesis and histologic features
- The mucinoses
- Generalized myxedema
- Clinical features
- Histologic features
- Localized (pretibial) myxedema
- Clinical features
- Pathogenesis and histologic features
- Lichen myxedematosus/scleromyxedema
- Clinical features
- Pathogenesis and histologic features
- Differential diagnosis
- Acral persistent papular mucinosis
- Clinical features
- Histologic features
- Cutaneous mucinosis of infancy
- Clinical features
- Histologic features
- Self-healing juvenile cutaneous mucinosis
- Clinical features
- Pathogenesis and histologic features
- Reticular erythematous mucinosis
- Scleredema
- Clinical features
- Pathogenesis and histologic features
- Differential diagnosis
- Papular and nodular cutaneous mucinosis of systemic lupus erythematosus
- Clinical features
- Histologic features
- Myxoid cyst
- Clinical features
- Histologic features
- Cutaneous focal mucinosis
- Clinical features
- Histologic features
- Differential diagnosis
- Nodular mucinosis of the breast
- Clinical features
- Histologic features
- Differential diagnosis
- Mucinous nevus
- Clinical features
- Histologic features
- Differential diagnosis
- Neuropathia mucinosa cutanea
- Self-healing infantile familial cutaneous mucinosis
- Localized mucinosis secondary to venous insufficiency
- Hereditary progressive mucinous histiocytosis
- Clinical features
- Pathogenesis and histologic features
- Differential diagnosis
- Secondary cutaneous mucinoses
- Clinical features
- Histologic features
- Acanthosis nigricans
- Clinical features
- Pathogenesis and histologic features
- Acrodermatitis enteropathica
- Clinical features
- Pathogenesis and histologic features
- Differential diagnosis
- Necrolytic migratory erythema
- Clinical features
- Pathogenesis and histologic features
- Differential diagnosis
- Bullosis diabeticorum
- Clinical features
- Pathogenesis and histologic features
- Differential diagnosis
- Chapter 15. Cutaneous adverse reactions to drugs
- Adverse drug reactions – introduction
- Type A drug reactions
- Type B drug reactions
- Type C drug reactions
- Adverse drug reactions – clinical manifestations
- Exanthematous reactions
- Urticarial reactions, angioedema, and anaphylaxis
- Serum sickness/serum sickness-like drug reactions
- Phototoxic and photoallergic reactions
- Drug reaction with eosinophilia and systemic symptoms
- Symmetric drug-related intertriginous and flexural exanthem
- Lichenoid and interface drug reactions
- Fixed drug eruptions
- Erythema multiforme
- Stevens-Johnson syndrome and toxic epidermal necrolysis
- Drug-induced hyperpigmentation
- Vasculitic drug reactions
- Purpuric drug reactions
- Granulomatous drug reactions
- Drug-induced panniculitis
- Drug-induced alopecia
- Drug-induced lupus erythematosus
- Bullous drug reactions
- Drug-induced linear IgA disease
- Drug-induced bullous pemphigoid
- Drug-induced epidermolysis bullosa acquisita
- Drug-induced pemphigus
- Drug-induced pseudoporphyria
- Psoriasiform drug reactions
- Pityriasiform drug reactions
- Pustular drug reactions
- Ichthyosiform drug reactions
- Drug-induced pseudolymphoma
- Drug-induced mucinosis
- Specific drug reactions
- Arsenic
- Iododerma
- Bromoderma
- Warfarin
- Heparin
- Penicillamine
- Gold
- Silver
- Mercury
- Bismuth
- Barbiturates and coma blisters
- Cutaneous reactions to oncologic agents
- Cutaneous reactions to chemotherapy
- Cutaneous reactions to targeted therapy
- Cutaneous reactions to checkpoint inhibition
- Adverse reactions to cytokine therapy
- Dental amalgam tattoos
- Esthetic microimplants
- Aluminum granuloma
- Adverse reactions to corticosteroid injections
- EMLA cream (prilocaine-lidocaine emulsion)
- Chapter 16. Neutrophilic and eosinophilic dermatoses
- Pyoderma gangrenosum
- Acute febrile neutrophilic dermatosis (Sweet syndrome)
- Neutrophilic dermatoses associated with gastrointestinal and hepatobiliary disease
- Rheumatoid neutrophilic dermatitis
- Arthropod and arachnid bite reactions
- Seabather’s eruption and coelenterate stings
- Erythema marginatum rheumaticum
- Juvenile idiopathic arthritis and Still disease
- Urticaria
- Papular urticaria
- Neutrophilic urticarial dermatosis
- Hypereosinophilic syndrome
- Eosinophilic cellulitis
- Eosinophilic pustular folliculitis
- Incontinentia pigmenti
- Hidradenitis suppurativa
- Prurigo pigmentosa
- Autoinflammatory disease
- Chapter 17. Vascular diseases
- Introduction
- Leukocytoclastic vasculitis
- IgA vasculitis (Henoch-Schönlein purpura)
- Infantile acute hemorrhagic edema
- Urticarial vasculitis
- Granulomatosis with polyangiitis
- Eosinophilic granulomatosis with polyangiitis
- Microscopic polyangiitis
- Polyarteritis nodosa
- Lymphocytic thrombophilic arteritis
- Kawasaki disease (mucocutaneous lymph node syndrome)
- Granuloma faciale
- Erythema elevatum diutinum
- Behçet disease
- Thromboangiitis obliterans
- Giant cell arteritis (temporal arteritis)
- Juvenile temporal arteritis
- Takayasu arteritis
- Infection-related vasculitis
- Paraneoplastic vasculitis
- Vasculitis associated with palisaded neutrophilic and granulomatous dermatitis
- Lymphocytic vasculitis
- Atrophic papulosis
- Livedoid vasculopathy and atrophie blanche
- Dermatological manifestations of cholesterol crystal embolism, embolism from atrial myxoma, and injection of foreign material
- Disseminated intravascular coagulation
- Cryoglobulinemia
- Antiphospholipid syndrome and Sneddon syndrome
- Thrombotic thrombocytopenic purpura and hemolytic uremic syndrome
- Immune thrombocytopenic purpura
- Factor V (Leiden) mutation
- Hypergammaglobulinemic purpura
- Monogenic autoinflammatory diseases associated with vasculitis and vasculitis-like manifestations
- Superficial thrombophlebitis
- Mondor disease
- Senile (actinic) purpura
- Cocaine-related retiform purpura
- Cutaneous collagenous vasculopathy
- Chapter 18. Idiopathic connective tissue disorders
- Lupus erythematosus
- Systemic sclerosis
- Localized scleroderma (morphea)
- Atrophoderma of Pasini and Pierini
- Eosinophilic fasciitis
- Polymyositis/dermatomyositis
- Mixed connective tissue disease
- Relapsing polychondritis
- Volume Two
- Chapter 19. Infectious diseases of the skin
- Viral infections
- Common wart
- Plantar warts
- Plane warts
- Condyloma acuminatum
- Bowenoid papulosis
- Epidermodysplasia verruciformis
- Herpes simplex virus infections
- Varicella and herpes zoster
- Cytomegalovirus infections
- Exanthem subitum
- Measles
- Eruptive pseudoangiomatosis
- Diseases caused by orthopox viruses
- Diseases caused by parapox viruses
- Milker nodule
- Ecthyma contagiosum
- Infections caused by other parapox viruses
- Molluscum contagiosum
- Hand, foot, and mouth disease
- Viral hemorrhagic fevers
- COVID-19
- Trichodysplasia spinulosa
- Pruritic and dyskeratotic dermatosis associated with human polyomavirus 6 and 7
- Bacterial Infections
- Impetigo
- Cutaneous manifestations of acute rheumatic fever
- Erythema marginatum
- Rheumatic fever nodules
- Staphylococcal scalded skin syndrome
- Toxic shock syndrome
- Clinical features
- Pathogenesis and histologic features
- Erysipelas and cellulitis
- Necrotizing fasciitis
- Infective folliculitis
- Folliculitis keloidalis nuchae
- Pseudofolliculitis
- Meningococcal septicemia
- Gonorrhea
- Plague
- Cutaneous anthrax
- Brucellosis
- Diseases caused by Bartonella species
- Cat scratch disease
- Trench fever
- Bartonellosis
- Bacillary angiomatosis
- Lyme disease
- Endemic (nonvenereal) treponematoses
- Endemic syphilis
- Yaws
- Pinta
- Tuberculosis
- Tuberculids
- Cutaneous complications of bacille Calmette-Guérin vaccination
- Nontuberculous environmental mycobacterial infections
- Leprosy
- Rhinoscleroma
- Nocardiosis
- Botryomycosis
- Malakoplakia
- Actinomycosis
- Whipple disease
- Erythrasma
- Trichobacteriosis
- Pitted keratolysis
- Cutaneous diphtheria
- Sago palm disease
- Tularemia
- Infections caused by Rickettsiae
- Protozoal infections
- Leishmaniasis
- Amebiasis cutis
- Infections caused by free-living amebae
- Toxoplasmosis
- Algal infections
- Protothecosis
- Fungal Infections
- Tinea capitis
- Infections caused by Microsporum canis and Microsporum audouinii
- Kerion
- Endothrix infections
- Favus
- Black piedra
- White piedra
- Tinea corporis
- Tinea pedis and tinea cruris
- Nodular granulomatous perifolliculitis
- Diseases caused by Malassezia species
- Tinea versicolor
- Malassezia folliculitis
- Tinea nigra
- Candidiasis
- Aspergillosis
- Hyalohyphomycosis
- Blastomycosis
- Paracoccidioidomycosis
- Coccidioidomycosis
- Cryptococcosis
- Mucormycosis
- Entomophthoramycosis
- Chromoblastomycosis
- Mycetoma
- Pheohyphomycosis
- Alternariosis
- Histoplasmosis
- Emergomycosis
- Talaromycosis
- Sporotrichosis
- Lobomycosis
- Pneumocystosis
- Diseases caused by Mesomycetozoea
- Rhinosporidiosis
- Arthropod infestations
- Scabies
- Tungiasis
- Myiasis
- Nematode infestation
- Onchocerciasis
- Cutaneous larva migrans
- Strongyloidiasis
- Gnathostomiasis
- Trematode infestation
- Schistosomiasis
- Cestode infestation
- Cysticercosis
- Echinococcosis
- Sparganosis
- Chapter 20. Human immunodeficiency virus (HIV) and acquired immunodeficiency syndrome (AIDS)-associated cutaneous diseases
- Introduction
- Acute HIV exanthem
- HIV-associated papulosquamous dermatoses
- HIV-associated seborrheic dermatitis
- Clinical features
- Pathogenesis and histologic features
- HIV-associated psoriasis
- Clinical features
- Pathogenesis and histologic features
- HIV-associated pityriasis rubra pilaris
- Clinical features
- Pathogenesis and histologic features
- Xerosis
- Clinical features
- Pathogenesis and histopathology
- HIV-associated photodistributed eruptions
- HIV-associated lichenoid photoeruptions and chronic actinic dermatitis
- Clinical features
- Pathogenesis and histologic features
- HIV-associated granuloma annulare
- Clinical features
- Pathogenesis and histologic features
- HIV-associated porphyria cutanea tarda
- Clinical features
- Pathogenesis and histologic features
- HIV-associated pruritic papular eruption
- Clinical features
- Pathogenesis and histologic features
- Differential diagnosis
- HIV-associated eosinophilic folliculitis
- Clinical features
- Pathogenesis and histologic features
- Differential diagnosis
- HIV-associated vasculitic disorders
- Erythema elevatum diutinum
- Clinical features
- Pathogenesis and histologic features
- Microscopic polyangiitis-like and polyarteritis nodosa–like illnesses
- Clinical features
- Pathogenesis and histologic features
- HIV-associated Kawasaki-like syndrome
- Clinical features
- Pathogenesis and histologic features
- HIV-associated autoimmune bullous diseases
- Clinical features
- Pathogenesis and histologic features
- HIV-associated cutaneous mucinoses
- Clinical features
- Pathogenesis and histologic features
- Lichenoid reactions in HIV
- Clinical features
- Histologic features
- HIV interface dermatitis
- Other HIV-associated dermatoses
- Cutaneous infections
- Bacterial infections
- Viral infections
- Fungal infections
- Other infections and infestations
- Lipodystrophy in HIV
- Histologic features
- Neoplasia
- Immune reconstitution inflammatory syndrome
- Chapter 21. Disorders of pigmentation
- Disorders of hypopigmentation
- Vitiligo
- Vogt–Koyanagi–Harada disease
- Clinical features
- Pathogenesis and histologic features
- Idiopathic guttate hypomelanosis
- Clinical features
- Pathogenesis and histologic features
- Differential diagnosis
- Oculocutaneous albinism
- Oculocutaneous albinism type A1
- Pathogenesis
- Oculocutaneous albinism type 1b
- Pathogenesis
- Type 1b variants
- Type 2 oculocutaneous albinism
- Pathogenesis
- Type 3 oculocutaneous albinism
- Pathogenesis
- Oculocutaneous albinism type 4
- Pathogenesis
- Oculocutaneous albinism type 5
- Pathogenesis
- Oculocutaneous albinism type 6
- Pathogenesis
- Oculocutaneous albinism type 7
- Pathogenesis
- Histologic features (in all types of oculocutaneous albinism)
- Hermansky–Pudlak syndrome
- Clinical features
- Pathogenesis and histologic features
- Chédiak–Higashi syndrome
- Clinical features
- Pathogenesis and histologic features
- Griscelli syndrome
- Clinical features
- Pathogenesis and histologic features
- Differential diagnosis
- Elejalde syndrome
- Piebaldism
- Clinical features
- Pathogenesis and histologic features
- Waardenburg syndrome
- Clinical features
- Pathogenesis and histologic features
- Nevus anemicus
- Clinical features
- Pathogenesis and histologic features
- Nevus depigmentosus
- Clinical features
- Pathogenesis and histologic features
- Progressive macular hypomelanosis
- Clinical features
- Pathogenesis and histologic features
- Hypomelanosis of Ito
- Clinical features
- Pathogenesis and histologic features
- Differential diagnosis
- Pityriasis alba
- Clinical features
- Pathogenesis and histologic features
- Postinflammatory hypopigmentation
- Clinical features
- Pathogenesis and histologic features
- Disorders of hyperpigmentation
- Melasma
- Laugier–Hunziker syndrome
- Clinical features
- Pathogenesis and histologic features
- Differential diagnosis
- McCune–Albright syndrome
- Clinical features
- Pathogenesis and histologic features
- Reticulate pigmented anomaly of the flexures (Dowling–Degos disease)
- Clinical features
- Pathogenesis and histologic features
- Differential diagnosis
- Reticulate acropigmentation of Kitamura
- Clinical features
- Pathogenesis and histologic features
- Differential diagnosis
- Naegeli–Franceschetti–Jadassohn syndrome
- Clinical features
- Pathogenesis and histologic features
- Dermatopathia pigmentosa reticularis
- Clinical features
- Pathogenesis and histologic features
- Dyschromatosis symmetrica hereditaria
- Clinical features
- Pathogenesis and histologic features
- Peutz–Jeghers syndrome
- Clinical features
- Pathogenesis and histologic features
- Bannayan–Riley–Ruvalcaba syndrome
- Clinical features
- Pathogenesis and histologic features
- Cronkhite–Canada syndrome
- Clinical features
- Pathogenesis and histologic features
- Carney complex
- Clinical features
- Pathogenesis and histologic features
- LEOPARD syndrome
- Clinical features
- Pathogenesis and histologic features
- Linear and whorled hyperpigmentation
- Clinical features
- Pathogenesis and histologic features
- Postinflammatory hyperpigmentation
- Clinical features
- Pathogenesis and histologic features
- Acquired brachial cutaneous dyschromatosis
- Clinical features
- Pathogenesis and histologic features
- Riehl melanosis
- Clinical features
- Pathogenesis and histologic features
- Notalgia paresthetica
- Clinical features
- Pathogenesis and histologic features
- Differential diagnosis
- Diffuse melanosis associated with metastatic melanoma
- Clinical features
- Pathogenesis and histologic features
- Chapter 22. Diseases of collagen and elastic tissue
- Introduction
- Diseases of collagen: generalized disorders
- Ehlers-Danlos syndrome
- Clinical features
- Pathogenesis and histologic features
- Aplasia cutis congenita
- Clinical features
- Histologic features
- Focal dermal hypoplasia syndrome
- Clinical features
- Histologic features
- Angiofibromas (adenoma sebaceum) and tuberous sclerosis
- Clinical features
- Pathogenesis and histologic features
- Nephrogenic systemic fibrosis
- Clinical features
- Pathogenesis and histologic features
- Differential diagnosis
- Restrictive dermopathy
- Clinical features
- Pathogenesis and histologic features
- Diseases of collagen: localized disorders
- White fibrous papulosis
- Clinical features
- Histologic features
- Differential diagnosis
- Collagenoma
- Familial cutaneous collagenoma
- Clinical features
- Histologic features
- Differential diagnosis
- Eruptive collagenoma
- Clinical features
- Histologic features
- Differential diagnosis
- Isolated collagenoma
- Clinical features
- Histologic features
- Diseases of elastic tissue
- Cutis laxa
- Clinical features
- Pathogenesis and histologic features
- Pseudoxanthoma elasticum
- Clinical features
- Pathogenesis and histologic features
- Differential diagnosis
- Pseudoxanthoma elasticum and inherited hemolytic and other syndromes
- Periumbilical pseudoxanthoma elasticum
- Clinical features
- Pathogenesis and histologic features
- Late-onset focal dermal elastosis
- Clinical features
- Pathogenesis and histologic features
- Anetoderma
- Clinical features
- Pathogenesis and histologic features
- Differential diagnosis
- Perifollicular elastolysis, anetoderma-like scars, and papular acne scars
- Clinical features
- Histologic features
- Pseudoxanthoma elasticum-like papillary dermal elastolysis
- Clinical features
- Pathogenesis and histologic features
- Differential diagnosis
- Mid-dermal elastolysis
- Clinical features
- Pathogenesis and histologic features
- Differential diagnosis
- Linear focal elastosis
- Clinical features
- Pathogenesis and histologic features
- Striae distensae
- Clinical features
- Pathogenesis and histologic features
- Elastoma, elastic tissue nevus, and Buschke-Ollendorff syndrome
- Clinical features
- Pathogenesis and histologic features
- Papular elastorrhexis
- Clinical features
- Pathogenesis and histologic features
- Differential diagnosis
- Cutaneous effects of chronic sun damage and chronological aging
- Clinical features
- Pathogenesis and histologic features
- Glucocorticoid-related cutaneous atrophy
- Hutchinson-Gilford syndrome
- Clinical features
- Pathogenesis and histologic features
- Werner syndrome
- Clinical features
- Pathogenesis and histologic features
- Radiation dermatitis
- Clinical features
- Histologic features
- Differential diagnosis
- Proteus syndrome
- Clinical features
- Pathogenesis and histologic features
- Chapter 23. Diseases of the hair
- Introduction
- Diagnosis, history, and laboratory tests
- Scalp biopsy and hair biopsy report
- Hair biopsy report
- Embryology and anatomy of the normal hair follicle
- Embryology
- Hair cycle
- Classification of alopecia
- Nonscarring alopecias
- Androgenetic alopecia
- Clinical features
- Pathogenesis and histologic features
- Differential diagnosis
- Telogen effluvium
- Clinical features
- Pathogenesis and histologic features
- Differential diagnosis
- Alopecia in patients with COVID-19
- Anagen effluvium
- Histologic features
- Loose anagen hair syndrome
- Clinical features
- Pathogenesis and histologic features
- Differential diagnosis
- Short anagen syndrome
- Clinical features
- Pathogenesis and histologic features
- Differential diagnosis
- Alopecia areata
- Clinical features
- Pathogenesis and histologic features
- Temporal triangular alopecia
- Clinical features
- Pathogenesis and histologic features
- Differential diagnosis
- Psoriatic alopecia and psoriatic scarring alopecia
- Clinical features
- Pathogenesis and histologic features
- Differential diagnosis
- Traumatic alopecias
- Trichotillomania
- Clinical features
- Histologic features
- Differential diagnosis
- Traction alopecia
- Clinical features
- Histologic features
- Differential diagnosis
- Pressure alopecia
- Senescent (senile) alopecia
- Clinical features
- Pathogenesis and histologic features
- Differential diagnosis
- Syphilitic alopecia
- Clinical features
- Pathogenesis and histologic features
- Differential diagnosis
- Lipedematous alopecia and lipedematous scalp
- Clinical features
- Pathogenesis and histologic features
- Differential diagnosis
- Scarring alopecias
- Scalp biopsies in scarring (cicatricial) alopecia
- Pathogenesis
- Classification of scarring alopecias
- Lupus erythematosus
- Clinical features
- Pathogenesis and histologic features
- Differential diagnosis
- Lichen planopilaris
- Classic lichen planopilaris
- Clinical features
- Pathogenesis and histologic features
- Differential diagnosis
- Frontal fibrosing alopecia
- Clinical features
- Pathogenesis and histologic features
- Differential diagnosis
- Clinical features
- Pathogenesis and histologic features
- Differential diagnosis
- Clinical features
- Clinical features
- Pathogenesis and histologic features
- Differential diagnosis
- Pseudopélade of Brocq
- Clinical features
- Pathogenesis and histologic features
- Differential diagnosis
- Central centrifugal cicatricial alopecia
- Clinical features
- Pathogenesis and histologic features
- Differential diagnosis
- Alopecia mucinosa
- Keratosis follicularis spinulosa decalvans
- Neutrophilic-associated primary scarring alopecias
- Folliculitis decalvans
- Clinical features
- Pathogenesis and histologic features
- Differential diagnosis
- Folliculitis decalvans and lichen planopilaris phenotypic spectrum
- Dissecting cellulitis of the scalp
- Clinical features
- Pathogenesis and histologic features
- Differential diagnosis
- Mixed primary scarring alopecias
- Acne keloidalis nuchae
- Clinical features
- Pathogenesis and histologic features
- Differential diagnosis
- Acne necrotica
- Clinical features
- Pathogenesis and histologic features
- Differential diagnosis
- Erosive pustular dermatosis
- Clinical features
- Pathogenesis and histologic features
- Differential diagnosis
- Nonspecific scarring alopecias
- Hair shaft DISORDERS
- Fractures of the hair shaft
- Trichorrhexis nodosa
- Clinical features
- Pathogenesis and histologic features
- Differential diagnosis
- Trichothiodystrophy
- Clinical features
- Pathogenesis and histologic features
- Trichoschisis and trichoclasis
- Trichorrhexis invaginata
- Clinical features
- Pathogenesis and histologic features
- Differential diagnosis
- Tapered fracture
- Clinical features
- Trichoptilosis
- Clinical features
- Pathogenesis and histologic features
- Differential diagnosis
- Irregularities of the hair shaft
- Uncombable hair syndrome
- Clinical features
- Pathogenesis and histologic features
- Differential diagnosis
- Pili bifurcati
- Clinical features
- Differential diagnosis
- Pili multigemini
- Clinical features
- Histologic features
- Differential diagnosis
- Trichostasis spinulosa
- Clinical features
- Pathogenesis and histologic features
- Differential diagnosis
- Virus-associated trichodysplasia spinulosa
- Pili annulati
- Clinical features
- Pathogenesis and histologic features
- Differential diagnosis
- Monilethrix
- Clinical features
- Pathogenesis and histologic features
- Differential diagnosis
- Bubble hair
- Hair shaft coiling and twisting
- Pili torti
- Clinical features
- Pathogenesis and histologic features
- Differential diagnosis
- Woolly hair
- Clinical features
- Histologic features
- Acquired progressive kinking of the hair
- Clinical features
- Pathogenesis and histologic features
- Trichonodosis (knotted hair)
- Clinical features
- Histologic features
- Circled and rolled hair
- Extraneous matter on the hair shaft
- Hair casts
- Pathogenesis and histologic features
- Differential diagnosis
- Miscellaneous follicular dermatoses
- Acne vulgaris
- Chloracne
- Clinical features
- Pathogenesis and histologic features
- Acne fulminans
- Clinical features
- Pathogenesis and histologic features
- Acne aestivalis
- Clinical features
- Histologic features
- Rosacea
- Clinical features
- Pathogenesis and histologic features
- Differential diagnosis
- Rosacea fulminans
- Clinical features
- Pathogenesis and histologic features
- Neutrophilic sebaceous adenitis
- Clinical features
- Pathogenesis and histologic features
- Pseudofolliculitis
- Clinical features
- Pathogenesis and histologic features
- Gram-negative folliculitis
- Clinical features
- Pathogenesis and histologic features
- Chapter 24. Diseases of the nails
- Introduction
- Anatomy and physiology of the nail apparatus
- Nail biopsy
- Histology of the normal nail
- Infectious diseases of the nail
- Onychomycosis
- Periungual warts and other nail infections
- Inflammatory diseases of the nail
- Psoriasis
- Lichen planus
- Trachyonychia
- Lichen striatus
- Darier–White disease
- Pemphigus vulgaris
- Melanocytic lesions of the nail apparatus
- Melanocytes in the nail unit
- Longitudinal melanonychia (melanonychia striata)
- Melanocytic activation
- Lentigo and nevus
- Blue nevus
- Melanoma
- Nonmelanocytic tumors of the nail apparatus
- Epithelial tumors
- Subungual epidermoid cysts
- Onychopapilloma
- Nail matrix and nail bed acanthoma
- Subungual (distal digital) keratoacanthoma
- Basal cell carcinoma
- Squamous cell carcinoma of the nail apparatus
- Fibroepithelial tumors
- Onychomatricoma
- Ungual fibrokeratoma and fibroma
- Soft tissue and bone tumors
- Superficial acral fibromyxoma
- Myxoid pseudocyst
- Lobular capillary hemangioma (pyogenic granuloma)
- Glomus tumor
- Subungual exostosis
- Chapter 25. Tumors of the surface epithelium
- Epidermal nevi
- Schimmelpenning syndrome
- Nevus comedonicus syndrome
- Pigmented hairy epidermal nevus syndrome
- Angora hair nevus syndrome
- Proteus syndrome
- Type 2 segmental Cowden disease
- FGFR3 epidermal nevus syndrome
- CHILD syndrome
- Phakomatosis pigmentokeratotica
- Inflammatory linear verrucous epidermal nevus syndrome
- Cutaneous skeletal hypophosphatemia syndrome
- Histologic features
- Cornu cutaneum
- Acanthoma fissuratum
- Clinical features
- Histologic features
- Seborrheic keratosis
- Clinical features
- Pathogenic and histologic features
- Dermatosis papulosa nigra
- Clinical features
- Pathogenesis and histologic features
- Solar lentigo
- Clinical features
- Histologic features
- Large cell acanthoma
- Clinical features
- Pathogenesis and histologic features
- Differential diagnosis
- Stucco keratoses
- Clinical features
- Pathogenesis and histologic features
- Differential diagnosis
- Intraepidermal epithelioma of Borst–Jadassohn
- Porokeratoma
- Clinical features
- Histologic features
- Psoriasiform keratosis
- Clinical features
- Histologic features
- Granular parakeratotic acanthoma
- Clinical findings
- Histologic features
- Clear cell acanthoma
- Clinical features
- Pathogenesis and histologic features
- Pseudoepitheliomatous hyperplasia
- Clinical features
- Histologic features
- Basal cell carcinoma
- Clinical features
- Ulcerative variant
- Nodulocystic variant
- Diffuse variant
- Superficial variant
- Pigmented variant
- Giant basal cell carcinoma
- Pathogenesis and histologic features
- Nodulocystic basal cell carcinoma
- Adenoid basal cell carcinoma
- Micronodular basal cell carcinoma
- Infiltrative basal cell carcinoma
- Morpheaform (sclerosing) basal cell carcinoma
- Keratotic basal cell carcinoma
- Basosquamous (metatypical) basal cell carcinoma
- Pigmented basal cell carcinoma
- Superficial basal cell carcinoma
- Ulcerative basal cell carcinoma
- Rare variants
- Pleomorphic (giant cell, with monster cells) basal cell carcinoma
- Clear cell basal cell carcinoma
- Signet ring cell basal cell carcinoma
- Granular basal cell carcinoma
- Basal cell carcinoma with differentiation toward adnexal structures
- Infundibulocystic basal cell carcinoma
- Metaplastic basal cell carcinoma
- Basal cell carcinoma with matrical differentiation (shadow cell basal cell carcinoma)
- Keloidal basal cell carcinoma
- Basal cell carcinoma with thickened basement membrane
- Basal cell carcinoma with neuroid-type nuclear palisading
- Nevoid basal cell carcinoma syndrome
- Clinical features
- Histologic features
- Differential diagnosis
- Bazex–Dupré–Christol and Rombo syndromes
- Clinical features
- Histologic features
- Fibroepithelioma of Pinkus
- Clinical features
- Histologic features
- Actinic keratoses
- Clinical features
- Pathogenesis and histologic features
- Differential diagnosis
- Squamous carcinoma in situ (Bowen disease)
- Clinical features
- Pathogenesis and histologic features
- Differential diagnosis
- PUVA keratosis
- Clinical features
- Histologic features
- Arsenical keratoses
- Clinical features
- Histologic features
- Squamous cell carcinoma
- Clinical features
- Pathogenesis and histologic features
- Radiation
- Immunosuppressive agents
- Human papillomavirus
- Chemical carcinogens
- Chronic inflammation and chronic infection
- Association with BRAF inhibitors
- Differentiation of squamous cell carcinoma
- Differential diagnosis
- Variants of squamous cell carcinoma
- Clear cell and signet ring cell squamous carcinoma
- Clinical features
- Histologic features
- Differential diagnosis
- Spindle cell squamous carcinoma
- Clinical features
- Pathogenesis and histologic features
- Differential diagnosis
- Desmoplastic squamous cell carcinoma
- Clinical features
- Pathogenesis and histologic features
- Differential diagnosis
- Acantholytic squamous cell carcinoma
- Clinical features
- Pathogenesis and histologic features
- Differential diagnosis
- Pseudovascular squamous cell carcinoma
- Clinical features
- Pathogenesis and histologic features
- Adenosquamous carcinoma/mucoepidermoid carcinoma of skin
- Clinical features
- Pathogenesis and histologic features
- Differential diagnosis
- Verrucous carcinoma
- Clinical features
- Pathogenesis and histologic features
- Differential diagnosis
- Keratoacanthoma
- Clinical features
- Pathogenesis and histologic features
- Differential diagnosis
- Metaplastic carcinoma of the skin (carcinosarcoma, carcinoma with heterologous differentiation)
- Clinical features
- Pathogenesis and histologic features
- Differential diagnosis
- Squamous cell carcinoma with chronic lymphocytic leukemia
- Xeroderma pigmentosum
- Clinical features
- Histologic features
- Merkel cell carcinoma
- Clinical features
- Pathogenesis and histologic features
- Differential diagnosis
- Lymphoepithelioma-like carcinoma of the skin
- Clinical features
- Pathogenesis and histologic features
- Differential diagnosis
- Chapter 26. Melanocytic nevi and melanoma
- GENERAL INTRODUCTION
- Pigmented Lesions without Neoplastic Melanocytes
- Ephelide
- Clinical features
- Histologic features
- Ink spot lentigo
- Histologic features
- PUVA and sunbed lentigines
- Clinical features
- Pathogenesis and histologic features
- Cutaneous melanoacanthoma
- Labial melanotic macule and labial lentigo
- Anogenital melanosis
- Genital lentiginosis
- Centrofacial lentiginosis
- Clinical features
- Histologic features
- Becker nevus
- Clinical features
- Pathogenesis and histologic features
- Carney complex
- Laugier-Hunziker syndrome
- Multiple lentigines syndrome
- Peutz-Jeghers syndrome
- Melanocytic Neoplasia
- Introduction
- Lentigo simplex
- Clinical features
- Histologic features
- The low cumulative sun-damage pathway
- Common acquired melanocytic nevus
- Clinical features
- Histologic features
- Molecular features
- Differential diagnosis
- Variants of common acquired melanocytic nevi
- Eccrine-centered nevus
- Clinical features
- Histologic features
- Melanocytic nevus of special sites
- Nevi on the scalp
- Clinical features
- Histologic features
- Nevi in and around the ear
- Histologic features
- Nevi of the breast
- Histologic features
- Nevi of flexural skin
- Histologic features
- Nevi of the lower leg/ankle
- Histologic features
- Differential diagnosis
- Acral nevus
- Clinical features
- Histologic features
- Molecular features
- Differential diagnosis
- Balloon cell nevus
- Clinical features
- Histologic features
- Differential diagnosis
- Cockarde nevus
- Clinical features
- Histologic features
- Histologic patterns that can complicate the diagnosis of melanocytic tumors
- Pseudomelanocytic nests
- Clinical and histologic features
- Histologic features
- Differential diagnosis
- Halo phenomenon
- Clinical features
- Histologic features
- Differential diagnosis
- Meyerson nevus
- Clinical features
- Histologic features
- Differential diagnosis
- Recurrent and sclerosing nevus
- Clinical features
- Histologic features
- Differential diagnosis
- Dysplastic nevi and dysplastic nevus syndrome
- Clinical features
- Pathogenesis and histologic features
- Differential diagnosis
- Melanocytomas of the low-CSD pathway
- Combined melanocytic nevus
- Clinical features
- Histologic features
- Differential diagnosis
- WNT-activated deep penetrating/plexiform melanocytoma (nevus)
- Clinical features
- Histologic features
- Differential diagnosis
- BAP1-inactivated melanocytoma
- Clinical features
- Histologic features
- PRKAR1A-inactivated (pigmented epithelioid) melanocytoma
- Clinical features
- Histologic features
- Differential diagnosis
- BRAF mutated and morphologically spitzoid tumors (BAMS)
- MAP2K1 mutated melanocytic tumors
- Low cumulative sun-induced damage (CSD) melanoma
- Clinical features
- Histologic features
- Molecular features
- The high cumulative sun-induced damage pathway
- Atypical (dysplastic) lentiginous nevus of the elderly
- Clinical features
- Histologic features
- Differential diagnosis
- Desmoplastic nevus on chronic sun-damaged skin
- Histologic features
- Differential diagnosis
- Lentigo maligna
- Clinical features
- Histologic features
- Differential diagnosis
- Desmoplastic melanoma
- Clinical features
- Histologic features
- Molecular features
- Differential diagnosis
- Spitz pathway
- Spitz nevus
- Clinical features
- Histologic features
- Molecular features
- Histological variants of Spitz nevi
- Differential diagnosis
- Desmoplastic Spitz nevus
- Clinical features
- Histologic features
- Differential diagnosis
- Pigmented spindle cell nevus of Reed
- Clinical features
- Histologic features
- Differential diagnosis
- Pigmented epithelioid cell nevus
- Clinical features
- Histologic features
- Differential diagnosis
- Pagetoid Spitz nevus
- Clinical features
- Histologic features
- Differential diagnosis
- Atypical Spitz tumor
- Spitz melanocytoma (atypical Spitz tumor)
- Histologic features
- Molecular features
- Spitz melanoma
- Clinical features
- Histologic features
- Molecular features
- Differential diagnosis
- Ancillary techniques in Spitz melanocytic proliferations
- Immunohistochemistry
- Acral melanoma pathway
- Acral nevus
- Acral (lentiginous) melanoma
- Histologic features
- Molecular features
- Genital and mucosal melanocytic tumors
- Genital melanocytic nevi
- Mucosal melanoma
- Molecular features
- Blue nevus and related tumors (blue nevus pathway)
- Dermal melanocytic lesions (dermal melanocytoses)
- Congenital dermal melanocytosis
- Clinical features
- Histologic features
- Differential diagnosis
- Nevus of Ota
- Clinical features
- Histologic features
- Differential diagnosis
- Nevus of Ito
- Clinical features
- Histologic features
- Sun nevus
- Clinical features
- Histologic features
- Hori nevus
- Clinical features
- Histologic features
- Common blue nevus
- Clinical features
- Histologic features
- Molecular features
- Differential diagnosis
- Patch-like blue nevus
- Target blue nevus
- Clinical features
- Pathogenesis and histologic features
- Plaque-like blue nevus
- Clinical features
- Histologic features
- Sclerosing (desmoplastic) blue nevus
- Compound blue nevus
- Clinical features
- Histologic features
- Hypopigmented common blue nevus
- Clinical features
- Histologic features
- Blue nevus with epithelioid cell features
- Clinical features
- Histologic features
- Epithelioid and fusiform blue nevus of chronically sun-damaged skin
- Clinical features
- Histologic features
- Differential diagnosis
- Neurocristic hamartoma
- Clinical features
- Histologic features
- Differential diagnosis
- Cellular blue nevus
- Clinical features
- Histologic features
- Differential diagnosis
- Blue nevus with PKC gene fusion
- Clinical features
- Histologic features
- Atypical cellular blue nevus
- Clinical features
- Histologic features
- Differential diagnosis
- Melanocytomas of the blue nevus pathway
- Melanoma arising from blue nevus
- Clinical features
- Histologic features
- Uveal and CNS melanocytic tumors
- Congenital melanocytic nevus pathway
- Congenital melanocytic nevi
- Clinical features
- Histologic features
- Molecular features
- Differential diagnosis
- Congenital nevi in neonates and young children
- Histologic features
- Giant congenital melanocytic nevi
- Clinical features
- Histologic features
- Molecular features
- Nevus spilus
- Clinical features
- Histologic features
- Molecular features
- Proliferative nodule in congenital nevus
- Clinical features
- Histologic features
- Differential diagnosis
- Melanoma arising in congenital nevus
- Pediatric melanoma
- Clinical features
- Histologic features
- Differential diagnosis
- Morphologic subtypes of melanoma not limited to a specific pathway
- Nodular melanoma
- Spitzoid melanoma
- Signet ring cell melanoma
- Rhabdoid melanoma
- Balloon and clear cell melanoma
- Myxoid melanoma
- Melanoma with neuroendocrine differentiation
- Adenoid and pseudopapillary melanoma
- Angiotropic and angiomatoid (pseudovascular) melanoma
- Transdifferentiated melanoma (melanoma with heterologous differentiation)
- Primary dermal melanoma
- Clinical features
- Histologic features
- Nested melanoma
- Nevoid melanoma
- Small cell melanoma
- Dermal squamomelanocytic tumor
- Clinical features
- Histologic features
- Basomelanocytic tumor
- Clinical features
- Histologic features
- Epidermotropic metastatic melanoma
- Blue nevus-like metastatic melanoma
- MELANOCYTIC TOOLS AND CONCEPTS
- Immunohistochemical assessment of melanocytic tumors
- Diagnostic uncertainty in melanocytic tumors
- Superficial atypical melanocytic proliferations of unknown significance
- Histologic features
- Comment
- Melanocytic tumors of uncertain malignant potential (MELTUMP)
- Clinical features
- Histologic features
- Biological behavior
- Comment
- Prognostic indicators
- Emerging concepts in metastatic melanoma
- Treatment of melanoma
- BRAF inhibitors
- KIT inhibitors
- NTRK inhibitors
- Immunotherapy
- Combination approaches
- Emerging treatments in melanoma
- Chapter 27. Tumors of the conjunctiva
- Introduction
- Anatomy and histology of the conjunctiva
- Diagnostic approaches
- Classification
- Congenital lesions
- Epibulbar choristoma (dermoid, dermolipoma, complex choristoma)
- Clinical features
- Histologic features
- Epibulbar osseous choristoma
- Clinical features
- Histologic features
- Epithelial tumors
- Squamous papilloma and inverted papilloma
- Clinical features
- Histologic features
- Hereditary benign intraepithelial dyskeratosis
- Clinical features
- Histologic features
- Oncocytoma
- Clinical features
- Histologic features
- Epithelial cysts
- Clinical features
- Histologic features
- Conjunctival squamous intraepithelial neoplasia and squamous cell carcinoma
- Clinical features
- Histologic features
- Adenosquamous carcinoma
- Clinical features
- Histologic features
- Melanocytic tumors
- Conjunctival nevus
- Clinical features
- Histologic features
- Blue nevus
- Clinical features
- Histologic features
- Inflamed juvenile conjunctival nevus
- Clinical features
- Histologic features
- Congenital melanosis oculi (congenital ocular melanocytosis)
- Clinical features
- Histologic features
- Benign epithelial melanosis
- Clinical features
- Histologic features
- Primary acquired melanosis (also called conjunctival melanocytic intraepithelial lesions)
- Clinical features
- Pathogenesis and histologic features
- Differential diagnosis
- Conjunctival melanoma
- Clinical features
- Pathogenesis and histologic features
- Differential diagnosis
- Hematolymphoid tumors
- Reactive lymphoid hyperplasia
- Clinical features
- Pathogenesis and histologic features
- Conjunctival lymphoma
- Clinical features
- Pathogenesis and histologic features
- Juvenile xanthogranuloma
- Clinical features
- Histologic features
- Conjunctival stromal tumors
- Vascular tumors
- Lobular capillary hemangioma
- Clinical features
- Histologic features
- Lymphangiectasia
- Clinical features
- Histologic features
- Conjunctival lymphangioma
- Clinical features
- Histologic features
- Kaposi sarcoma
- Clinical features
- Histologic features
- Fibrous tumors
- Benign fibrous histiocytoma
- Clinical features
- Histologic features
- Conjunctival myxoma
- Clinical features
- Histologic features
- Neural tumors
- Neurofibroma
- Clinical features
- Histologic features
- Schwannoma (neurilemmoma)
- Clinical features
- Histologic features
- Granular cell tumor
- Clinical features
- Histologic features
- Myogenic tumors
- Rhabdomyosarcoma
- Clinical features
- Histologic features
- Adipocytic tumors
- Clinical features
- Histologic features
- Other tumorlike lesions
- Pinguecula and pterygium
- Clinical features
- Histologic features
- Amyloidosis
- Clinical features
- Histologic features
- Metastatic and secondary tumors
- Metastatic tumors
- Secondary tumors
- Tumors of the caruncle
- Chapter 28. Sentinel lymph node biopsies
- Introduction and background
- Who should be offered a sentinel lymph node biopsy
- Laboratory management and gross evaluation of sentinel nodes
- Confirmation of the sentinel status of submitted lymph nodes
- Can tissue from a sentinel node ethically be made available for research?
- Intraoperative evaluation of sentinel nodes
- Accurate interpretation of sentinel lymph node results
- The sentinel node lymph node protocol
- The role of immunohistochemistry in detecting tumor in sentinel nodes
- Microscopic evaluation of sentinel nodes for metastatic melanoma
- Separation of nevus cells and metastatic melanoma in sentinel nodes
- Is there a role for SNB in the evaluation of melanocytomas/melanocytic lesions of uncertain metastatic potential?
- Molecular biology techniques in the assessment of sentinel nodes from melanoma patients
- Prediction of outcome based on the extent of nodal replacement by tumor and its distribution within the sentinel node
- Pathological evaluation of nonsentinel nodes
- The impact of complete lymph node dissection after positive sentinel lymph node biopsy in melanoma-specific survival
- Lymphatic mapping and sentinel node biopsy for nonmelanocytic neoplasms
- Reporting the sentinel node
- Chapter 29. Cutaneous lymphoproliferative diseases and related disorders
- T-cell lymphomas
- Mycosis fungoides
- Transformation of mycosis fungoides
- Classic mycosis fungoides with unusual clinical manifestations
- Mycosis fungoides in children and adolescents
- Hypopigmented mycosis fungoides and hyperpigmented mycosis fungoides
- Papular mycosis fungoides
- Mycosis fungoides and ichthyosis
- Vesiculobullous mycosis fungoides
- Pustular and neutrophilic mycosis fungoides
- Pigmented purpura-like and cutaneous vasculitis-associated mycosis fungoides
- Palmoplantar mycosis fungoides
- Verrucous/hyperkeratotic mycosis fungoides
- Unilesional mycosis fungoides
- “Invisible” mycosis fungoides
- Mycosis fungoides with unusual histologic features
- Granulomatous mycosis fungoides
- Interstitial mycosis fungoides
- Syringotropic mycosis fungoides
- Mycosis fungoides with dermal mucin
- Distinct variants of mycosis fungoides
- Folliculotropic mycosis fungoides
- Follicular mucinosis and alopecia mucinosa
- Pagetoid reticulosis
- Granulomatous slack skin disease
- Sézary syndrome
- Primary cutaneous CD30-positive T-cell lymphoproliferative disorders
- Lymphomatoid papulosis
- Primary cutaneous anaplastic large cell lymphoma
- Primary cutaneous CD4-positive small/medium T-cell lymphoproliferative disorder
- Primary cutaneous acral CD8+ T-cell lymphoproliferative disorder
- Angioimmunoblastic T-cell lymphoma
- Adult T-cell leukemia/lymphoma
- Subcutaneous panniculitis-like T-cell lymphoma
- Extranodal NK/T-cell lymphoma, nasal type
- Primary cutaneous CD8-positive aggressive epidermotropic cytotoxic T-cell lymphoma
- EBV-positive lymphoproliferative diseases of childhood
- Severe mosquito bite allergy
- Hydroa vacciniforme lymphoproliferative disorder
- Primary cutaneous gamma/delta T-cell lymphoma
- Peripheral T-cell lymphoma, not otherwise specified
- Benign cutaneous infiltrates that can be mistaken for cutaneous lymphoma (reactive T-cell–rich lymphoid proliferations/cutaneous T-cell pseudolymphomas)
- Intravascular (intralymphatic) T-cell–rich lymphoid proliferation
- Angiomatoid T-cell–rich lymphoid proliferations
- Pseudolymphomatous angiokeratoma
- T-cell–rich angiomatoid polypoid pseudolymphoma
- Drug-induced T-cell–rich lymphoid proliferation
- Nodular reactive T-cell–rich lymphoid proliferations
- Pseudolymphomatous folliculitis
- Atypical cutaneous lymphoproliferative disorder of HIV infection
- Lymphocytic infiltrate of the skin (Jessner)
- Chronic actinic dermatitis
- B-cell lymphomas
- Primary cutaneous B-cell lymphoma
- Primary cutaneous marginal zone B-cell lymphoma
- Primary cutaneous follicle center lymphoma
- Primary cutaneous diffuse large B-cell lymphoma, leg type
- Primary cutaneous diffuse large B-cell lymphoma, other
- Secondary cutaneous involvement by B-cell lymphoma
- Mantle cell lymphoma
- B-chronic lymphocytic leukemia/small lymphocytic lymphoma
- Lymphomatoid granulomatosis
- Cutaneous manifestations of plasma cell myeloma and primary cutaneous plasmacytoma
- Intravascular large B-cell lymphoma
- Plasmablastic lymphoma
- Other B-cell lymphomas secondarily involving the skin
- Cutaneous manifestations of Hodgkin lymphoma
- Lymphoproliferative disorders and lymphomas associated with immunodeficiency and dysregulation
- Epstein–Barr virus-positive mucocutaneous ulcer
- Inborn error of immunity-associated lymphoproliferative disorders
- Benign cutaneous infiltrates that can be mistaken for cutaneous B-cell lymphoma (reactive cutaneous B-cell–rich lymphoid proliferations/cutaneous B-cell pseudolymphoma)
- Reactive B-cell–rich cutaneous lymphoid proliferation
- Cutaneous and systemic plasmacytosis
- IgG4-related disease
- Cutaneous Castleman disease
- Pretibial lymphoplasmacytic plaque
- Angioplasmocellular hyperplasia
- Histiocytic disorders
- Langerhans cell histiocytoses and other
- Cutaneous Kikuchi–Fujimoto disease
- Intralymphatic histiocytosis
- The histiocytoses
- Langerhans group of histiocytosis
- Langerhans cell histiocytosis
- Langerhans cell sarcoma
- Indeterminate dendritic cell tumor
- Congenital self-healing Langerhans cell histiocytosis
- Erdheim–Chester disease
- Non-langerhans cell cutaneous and mucocutaneous histiocytoses
- Xanthogranuloma family
- Juvenile xanthogranuloma
- Benign cephalic histiocytosis
- Generalized eruptive histiocytosis
- Xanthoma disseminatum and scalloped cell xanthogranuloma
- Papular xanthoma
- Progressive nodular histiocytosis and spindle cell xanthogranuloma
- Rosai–Dorfman disease
- Multicentric reticulohistiocytosis and reticulohistiocytoma (reticulohistiocytosis)
- ALK-positive histiocytosis
- Hemophagocytic lymphohistiocytosis
- Crystal-storing histiocytosis
- Follicular dendritic cell sarcoma and interdigitating dendritic cell sarcoma
- Histiocytic sarcoma
- Cutaneous leukemic infiltrates and precursor cell neoplasms
- Introduction
- Myeloid sarcoma
- Blastic plasmacytoid dendritic cell neoplasm
- Precursor lymphoblastic leukemia/lymphoma
- Cutaneous extramedullary hematopoiesis
- Mastocytosis
- Isolated and multilocalized cutaneous mastocytoma
- Maculopapular cutaneous mastocytosis/urticaria pigmentosa
- Diffuse cutaneous mastocytosis
- Cutaneous involvement in systemic mastocytosis
- Mast cell sarcoma
- Chapter 30. Cutaneous metastases and Paget disease of the skin
- Cutaneous metastases
- Individual tumors
- Squamous carcinoma
- Adenocarcinoma
- Mesothelioma
- Mammary and extramammary Paget disease
- Clinical features
- Pathogenesis and histologic features
- Differential diagnosis
- Chapter 31. Tumors of the hair follicle
- Hair nevi
- Hair follicle nevus
- Woolly hair nevus
- Comedo nevus
- Basaloid follicular hamartoma
- Dilated pore
- Pilar sheath acanthoma
- Follicular infundibulum tumor (infundibuloma)
- Trichoadenoma
- Trichilemmoma and Cowden disease
- Desmoplastic trichilemmoma
- Trichilemmal carcinoma
- Proliferating trichilemmal (pilar) cyst
- Pilomatrixoma
- Pilomatrix carcinoma
- Wnt/beta-catenin activated non pilomatrical carcinoma of the skin
- Clinical features
- Pathogenesis and histologic features
- Clinical features
- Pathogenesis and histologic features
- Differential diagnosis
- Trichofolliculoma
- Clinical features
- Pathogenesis and histologic features
- Folliculosebaceous cystic hamartoma
- Clinical features
- Pathogenesis and histologic features
- Differential diagnosis
- Sebaceous trichofolliculoma
- Clinical features
- Histologic features
- Differential diagnosis
- Trichoepithelioma
- Clinical features
- Pathogenesis and histologic features
- Differential diagnosis
- Desmoplastic trichoepithelioma (sclerosing epithelial hamartoma)
- Clinical features
- Histologic features
- Differential diagnosis
- Trichoblastoma
- Clinical features
- Histologic features
- Differential diagnosis
- Adamantinoid trichoblastoma (cutaneous lymphadenoma, lymphoepithelial tumor of the skin)
- Clinical features
- Pathogenesis and histologic features
- Differential diagnosis
- Malignant trichoblastoma
- Clinical features
- Histologic features
- Differential diagnosis
- Perifollicular fibroma
- Clinical features
- Pathogenesis and histologic features
- Fibrofolliculoma
- Clinical features
- Histologic features
- Trichodiscoma, Birt-Hogg-Dubé, and Hornstein-Knickenberg syndromes
- Clinical features
- Pathogenesis and histologic features
- Neurofollicular hamartoma (spindle cell predominant trichodiscoma)
- Clinical features
- Histologic features
- Chapter 32. Tumors and related lesions of the sebaceous glands
- Ectopic sebaceous glands
- Sebaceous hyperplasia
- Nevus sebaceus
- Steatocystoma and sebocystomatosis
- Sebaceous adenoma
- Sebaceous epithelioma
- Sebaceoma
- Superficial epithelioma with sebaceous differentiation
- Basal cell carcinoma with sebaceous differentiation
- Sebaceous carcinoma
- Muir-Torre syndrome
- Mantleoma
- Other cutaneous tumors showing sebaceous differentiation
- Chapter 33. Tumors of the sweat glands
- Apocrine nevus
- Apocrine hidrocystoma and apocrine cystadenoma
- Hybrid epidermoid and apocrine cyst
- Syringocystadenoma papilliferum
- Syringocystadenocarcinoma papilliferum
- Hidradenoma papilliferum
- Tubular apocrine adenoma
- Adenoma and adenocarcinoma of the anogenital mammary-like glands
- Nipple adenoma
- Syringomatous adenoma of the nipple
- Apocrine poroma
- Cutaneous oncocytoma
- Apocrine carcinoma
- Cribriform tumor (Primary cutaneous cribriform carcinoma)
- Ceruminous gland tumors
- Mixed tumor of the skin
- Malignant mixed tumor
- Myoepithelioma and malignant myoepithelioma
- Eccrine nevus
- Adnexal polyp of neonatal skin
- Eccrine syringofibroadenoma
- Eccrine angiomatous hamartoma
- Porokeratotic eccrine ostial and dermal duct nevus
- Eccrine hidrocystoma
- Benign poroid neoplasms
- Hidroacanthoma simplex
- Eccrine poroma
- Dermal duct tumor
- Eccrine porocarcinoma
- Syringoma
- Papillary eccrine adenoma
- Digital papillary adenocarcinoma
- Hidradenoma
- Hidradenocarcinoma
- Dermal cylindroma
- Malignant cylindroma
- Spiradenoma
- Spiradenocarcinoma
- Syringoid eccrine carcinoma
- Microcystic adnexal carcinoma
- Primary cutaneous adenoid cystic carcinoma
- Primary cutaneous mucinous carcinoma
- Endocrine mucin-producing sweat gland carcinoma
- Secretory carcinoma of the skin
- Microsecretory adenocarcinoma of the skin
- Nuclear protein in testis carcinoma of the skin
- Eccrine ductal carcinoma
- Squamoid eccrine ductal carcinoma
- Polymorphous sweat gland carcinoma
- Primary cutaneous signet ring cell carcinoma
- Chapter 34. Cutaneous cysts
- Follicular cysts
- Epidermoid cyst
- Clinical features
- Pathogenesis and histologic features
- Proliferating epidermoid cyst
- Clinical features
- Histologic features
- Hybrid cyst
- Verrucous cyst
- Clinical features
- Pathogenesis and histologic features
- Differential diagnosis
- Epidermoid cyst of the sole
- Clinical features
- Histologic features
- Comedonal cyst
- Clinical features
- Pathogenesis and histologic features
- Differential diagnosis
- Milia
- Clinical features
- Pathogenesis and histologic features
- Trichilemmal cyst
- Clinical features
- Pathogenesis and histologic features
- Vellus hair cysts
- Clinical features
- Pathogenesis and histologic features
- Differential diagnosis
- Dermoid cyst
- Clinical features
- Pathogenesis and histologic features
- Differential diagnosis
- Cutaneous mature cystic teratoma
- Glandular cysts
- Bronchogenic cyst
- Clinical features
- Pathogenesis and histologic features
- Thyroglossal duct cyst
- Clinical features
- Pathogenesis and histologic features
- Branchial cleft cyst
- Clinical features
- Pathogenesis and histologic features
- Cervical thymic cyst
- Clinical features
- Pathogenesis and histologic features
- Cutaneous ciliated cyst
- Clinical features
- Pathogenesis and histologic features
- Differential diagnosis
- Median raphe cyst
- Clinical features
- Pathogenesis and histologic features
- Differential diagnosis
- Cutaneous metaplastic synovial cyst
- Clinical features
- Pathogenesis and histologic features
- Pilonidal sinus
- Clinical features
- Pathogenesis and histologic features
- Dental sinus
- Clinical features
- Histologic features
- Mucinous syringometaplasia
- Clinical features
- Pathogenesis and histologic features
- Umbilical polyp and granuloma
- Clinical features
- Histologic features
- Pseudocyst of the auricle
- Clinical features
- Pathogenesis and histologic features
- Chapter 35. Connective tissue tumors
- Introduction
- Adipocytic Tumors
- Benign adipocytic tumors and tumor-like lesions
- Lipoma
- Nevus lipomatosus superficialis (Hoffman and Zurhelle)
- Lipomatosis
- Adiposis dolorosa
- Piezogenic pedal papules
- Lipomatosis of nerve
- Lipoblastoma/lipoblastomatosis
- Lipoblastoma-like tumor
- Angiolipoma
- Myolipoma
- Chondroid lipoma
- Spindle cell lipoma/pleomorphic lipoma
- Hibernoma
- Adipocytic tumors of intermediate malignancy (locally aggressive)
- Atypical lipomatous tumor
- Atypical spindle cell/pleomorphic lipomatous tumor
- Malignant adipocytic tumors
- Liposarcoma
- Tumors of Fibrous, Fibroblastic and Myofibroblastic Tissue
- Benign fibrous and myofibroblastic tumors and tumor-like lesions
- Hypertrophic scar
- Keloid
- Nodular fasciitis
- Proliferative fasciitis and proliferative myositis
- Fibro-osseous tumor of the digits
- Ischemic fasciitis
- Elastofibroma
- Fibroepithelial polyp (including pleomorphic fibroma)
- Dermatomyofibroma
- Storiform collagenoma
- Nuchal and nuchal-type fibroma
- Gardner fibroma
- Nuchal fibrocartilaginous pseudotumor
- Fibromatosis colli
- Calcifying fibrous tumor
- Fibroma of tendon sheath
- Desmoplastic fibroblastoma
- Inclusion body fibromatosis
- Calcifying aponeurotic fibroma
- Knuckle pad
- Acquired digital fibrokeratoma
- Superficial acral fibromyxoma
- Plaque-like CD34-positive dermal fibroma
- Fibrous hamartoma of infancy
- Fibroblastic connective tissue nevus
- Angiofibroma of soft tissue
- Mammary-type myofibroblastoma of soft tissue
- Juvenile hyaline fibromatosis
- EWSR1::SMAD3-positive fibroblastic tumor
- Palmar fibromatosis
- Plantar fibromatosis
- Penile fibromatosis
- Cutaneous myxoma
- Intermediate (locally aggressive) fibroblastic and myofibroblastic tumors
- Desmoid fibromatosis
- Lipofibromatosis
- Giant cell fibroblastoma
- Dermatofibrosarcoma protuberans
- Myxoinflammatory fibroblastic sarcoma
- Inflammatory myofibroblastic tumor
- Solitary fibrous tumor
- Giant cell angiofibroma
- Low-grade myofibroblastic sarcoma
- Infantile fibrosarcoma
- Superficial CD34-positive fibroblastic tumor
- Malignant fibroblastic tumors
- Fibrosarcoma: adult type
- Sclerosing epithelioid fibrosarcoma
- Low-grade fibromyxoid sarcoma
- Myxofibrosarcoma
- Fibrohistiocytic Tumors
- Benign fibrohistiocytic tumors and tumor-like lesions
- Fibrous papule
- Multinucleate cell angiohistiocytoma
- Dermatofibroma
- Deep benign fibrous histiocytoma
- Giant cell tumor of tendon sheath
- Fibrohistiocytic tumors of intermediate malignancy
- Giant cell tumor of soft tissue (and skin)
- Angiomatoid fibrous histiocytoma
- Plexiform fibrohistiocytic tumor
- Plexiform myofibroblastoma
- Nerve Sheath and Neuroectodermal Tumors and tumor-like Lesions
- Reactive lesions
- Traumatic neuroma
- Pacinian neuroma
- Morton neuroma
- Dermal hyperneury
- Epithelial sheath neuroma
- Neural hamartomas
- Mucosal neuroma
- Benign triton tumor
- Other hamartomas and choristomas
- Benign neural tumors
- Solitary circumscribed neuroma
- Schwannoma
- Hybrid schwannoma-perineurioma
- Neurofibroma
- Neurofibromatosis
- Granular cell tumor
- Congenital granular cell epulis
- Dermal nerve sheath myxoma
- Perineurioma
- NTRK-rearranged spindle cell neoplasm
- Heterotopias
- Meningeal heterotopias
- Glial heterotopias
- Malignant neural neoplasms
- Malignant peripheral nerve sheath tumor
- Smooth Muscle Tumors
- Smooth muscle hamartomas
- Congenital smooth muscle hamartoma
- Benign smooth muscle tumors
- Pilar leiomyoma
- Genital and nipple leiomyoma
- Intermediate and malignant smooth muscle tumors
- Atypical intradermal smooth muscle neoplasm and leiomyosarcoma
- Striated Muscle Tumors
- Striated muscle hamartomas
- Rhabdomyomatous mesenchymal hamartoma
- Benign striated muscle tumors
- Rhabdomyoma (extracardiac)
- Malignant striated muscle tumors
- Rhabdomyosarcoma
- Tumors of Vascular Origin
- Introduction
- Benign tumors including reactive vascular proliferations, malformations, and ectasias
- Intravascular papillary endothelial hyperplasia
- Reactive angioendotheliomatosis
- Congenital and infantile hemangiomas
- Rapidly involuting congenital hemangioma (RICH)
- Noninvoluting congenital hemangioma (NICH)
- Infantile hemangioma
- Infantile hemangiomas with minimal or arrested growth (abortive hemangiomas)
- Cherry angioma
- Lobular capillary hemangioma (pyogenic granuloma)
- Glomeruloid hemangioma
- Papillary hemangioma
- Thrombosing hemangioma with organizing/anastomosing features
- Symplastic hemangioma
- Angiokeratoma
- Verrucous venous malformation (verrucous hemangioma)
- Angiomatosis
- Nevus flammeus
- Cutis marmorata telangiectatica congenita
- Spider nevus
- Angioma serpiginosum
- Hereditary hemorrhagic telangiectasia
- Generalized essential telangiectasia
- Venous lake
- Arteriovenous hemangioma
- Cavernous hemangioma
- Microvenular hemangioma
- Epithelioid hemangioma
- Cutaneous epithelioid angiomatous nodule
- Spindle cell hemangioma
- Tufted angioma
- Acquired elastotic hemangioma
- Poikilodermatous plaque-like hemangioma
- Lymphatic tumors and proliferations
- Hobnail hemangioma
- Lymphangioma
- Kaposiform lymphangiomatosis
- Multifocal lymphangiomatosis with thrombocytopenia (cutaneovisceral angiomatosis with thrombocytopenia)
- Lymphangiomatosis
- Vascular tumors of low-grade or borderline malignancy
- Retiform hemangioendothelioma
- Papillary intralymphatic angioendothelioma
- Kaposiform hemangioendothelioma
- Kaposi sarcoma
- Composite hemangioendothelioma
- Pseudomyogenic hemangioendothelioma
- Malignant vascular tumors
- Epithelioid hemangioendothelioma
- YAP1::TFE3-fused hemangioendothelioma
- Angiosarcoma
- Radiation and lymphedema-associated vascular tumors
- Postradiation atypical vascular lesion
- Tumors of perivascular cells
- Glomus tumor
- Myopericytoma
- Myofibroma and myofibromatosis
- Angioleiomyoma
- Tumors of Bone and Cartilage-Forming Tissue
- Benign tumors of bone
- Osteoma cutis
- Malignant tumors of bone
- Extraskeletal osteosarcoma
- Benign reactive and neoplastic chondroid and cartilaginous lesions
- Accessory tragus
- Soft tissue chondroma
- Calcifying chondroid mesenchymal neoplasm
- Acral fibrochondromyxoid tumor
- Myoepithelioma-like hyalinizing epithelioid tumor
- Malignant chondroid and cartilaginous tumors
- Extraskeletal myxoid chondrosarcoma
- Mesenchymal chondrosarcoma
- Miscellaneous Reactive Conditions
- Synovial metaplasia
- Massive localized lymphedema
- Myxochondroid metaplasia of the plantar foot
- Benign Mesenchymal Neoplasms of Uncertain Differentiation
- Epithelioid fibrous histiocytoma
- Superficial ALK-rearranged myxoid spindle cell neoplasm
- Cellular neurothekeoma
- Nonneural granular cell tumor (primitive polypoid granular cell tumor)
- Meningioma-like tumor of the skin
- Ossifying plexiform tumor
- Phosphaturic mesenchymal tumor (mixed connective tissue variant)
- PRRX1-rearranged mesenchymal tumor
- Mesenchymal Tumors of Unknown Histogenesis of Intermediate Biologic Potential
- Ossifying fibromyxoid tumor
- Hemosiderotic fibrolipomatous tumor
- Pleomorphic hyalinizing angiectatic tumor
- Malignant Tumors of Uncertain Histogenesis
- Atypical fibroxanthoma and pleomorphic dermal sarcoma
- Undifferentiated sarcoma
- Epithelioid sarcoma
- Synovial sarcoma
- Alveolar soft part sarcoma
- Extrarenal rhabdoid tumor
- Undifferentiated round cell sarcomas
- Ewing sarcoma
- Round cell sarcoma with EWSR1-non-ETS fusions
- CIC-rearranged sarcoma
- Sarcoma with BCOR genetic alterations
- GLI1-altered soft tissue tumor
- Mesenchymal tumors with melanocytic differentiation
- Perivascular epithelioid cell tumor
- Clear cell sarcoma
- CRTC1::TRIM11 cutaneous tumor
- Mesenchymal tumors with melanocytic differentiation and ACTIN::MITF, MITF::CREM, or MED15::ATF1 fusions
- Cutaneous Metastasis of Sarcomas
- Chapter 36. Animal models of skin diseases
- Introduction
- One gene, one disease
- Comparative anatomy of the human and mouse skin and adnexa
- Specialized techniques for mouse skin
- Creation of models of human disease
- Examples of mouse models for human skin in health and disease
- Infectious diseases
- Botryomycosis
- Mouse papillomaviruses
- Vascular changes in the skin
- Genetic-based skin diseases
- Coat color genetics
- A locus
- B locus
- C locus
- D locus
- P locus
- Mouse models of melanoma
- Carcinogen-induced melanoma
- Genetically engineered mouse melanoma models
- Transgenic approaches
- Conditional cre-lox models
- Syngeneic mouse melanoma models
- Humanized mouse melanoma models
- Anhidrotic ectodermal dysplasia: mouse models that helped define the receptor-ligand concept
- Hairless, rhino, papular atrichia, and genocopies
- Alopecia areata
- Psoriasiform mouse models
- Xenografts: transplanting tissues from humans to mice
- Currently missing mouse models of human skin pathology
- Zebrafish as a model system to study skin biology and pathology
- Zebrafish skin development
- The zebrafish genome and genetic manipulation
- The zebrafish genome
- Forward genetics
- Morpholino-based knockdown of gene expression
- Genome editing in zebrafish
- Application of the zebrafish model for skin research
- Heritable skin disorders
- Wound healing and reepithelialization
- Melanoma and pigmentation
- Small-molecule and drug screening
- Accessing and using websites for mouse information
- Accessing and using websites for zebrafish information
- Summary
- Index