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Atlas of Dermatopathology

Synopsis and Atlas of Lever’s Pathology of the Skin
Edition: 4
9781975124663
ISBN/ISSN:
9781975124663
Publication Date:
May 6, 2020
2020-05-6
9781975124663
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Offering a highly visual, systematic approach to diagnosing skin diseases, Atlas of Dermatopathology: Synopsis and Atlas of Lever’s Histopathology of ...
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  • Offering a highly visual, systematic approach to diagnosing skin diseases, Atlas of Dermatopathology: Synopsis and Atlas of Lever’s Histopathology of the Skin, 4th Edition, is an ideal reference tool or teaching aid for dermatopathologists, pathologists, dermatologists, and trainees. This unique atlas uses a pattern-based approach to differential diagnosis, clearly organized according to what is seen on a microscopic slide. More than 1600 high-quality images assist in the understanding of cutaneous reaction patterns and diagnosis.
    • Classifies patterns according to location, reaction patterns, and cell type if applicable, including diseases that have been recently described.
    • Color-codes each chapter for consistency, helping you navigate quickly to the information you need.
    • Compares “look-alike” diseases in easy-to-reference tables.
    • Includes multiple color photomicrographs for each disease, in addition to providing an online image bank.


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  • Edition
    4
    ISBN/ISSN
    9781975124663
    Product Format
    Vitalsource Interactive eBook
    Table
    0
    Edition
    4
    Publication Date
    May 6, 2020
  • David Elder MB, ChB, FRCPA
    Professor and Associate Director, Division of Anatomic Pathology, Department of Pathology and Labratory Medicine, University of Pennsylvania School of Medicine
  • DETAILED CONTENTS
    How to Use This Book vii
    Preface xvii
    Preface to the First Edition xix
    Acknowledgments xxi
    Introduction xxiii
    Disorders Mostly Limited to
    the Epidermis and Stratum
    Corneum 1
    A. Hyperkeratosis With Hypogranulosis 1
    1. No Inflammation 1
    Ichthyosis Vulgaris 2
    B. Hyperkeratosis With Normal or Hypergranulosis 2
    1. No Inflammation 3
    X-Linked Ichthyosis 3
    Epidermolytic Hyperkeratosis 3
    Epidermodysplasia Verruciformis 5
    2. Scant Inflammation 6
    Lichen Amyloidosis and Macular Amyloidosis 7
    C. Hyperkeratosis With Parakeratosis 8
    1. Scant or No Inflammation 8
    Dermatophytosis 8
    Granular Parakeratosis 9
    D. Localized or Diffuse Hyperpigmentations 10
    1. No Inflammation 10
    Mucosal Melanotic Macules (Mucosal Lentigines) 11
    Ephelids (Freckles) 12
    2. Scant Inflammation 13
    Pityriasis (Tinea) Versicolor 13
    E. Localized or Diffuse Hypopigmentations 14
    1. With or Without Slight Inflammation 14
    Vitiligo 14
    References 16
    Localized Superficial
    Epidermal or Melanocytic
    Proliferations 17
    A. Localized Irregular Thickening of the Epidermis 18
    1. Localized Epidermal Proliferations 18
    I
    II
    Actinic Keratosis 18
    Eccrine Poroma 20
    Squamous Cell Carcinoma In Situ and Bowen Disease 20
    Bowenoid Papulosis 22
    Clear Cell Squamous Cell Carcinoma In Situ 23
    Clear Cell Acanthoma 23
    2. Superficial Melanocytic Proliferations 26
    Superficial Melanocytic Nevi and Melanomas 26
    Pigmented Spindle Cell Nevus 27
    Acral Melanoma 27
    B. Localized Lesions With Thinning
    of the Epidermis 30
    1. With Melanocytic Proliferation 30
    Lentigo Maligna Melanoma, In Situ or
    Microinvasive (High CSD) 30
    Recurrent (“Persistent”) Nevus, Lentiginous Patterns 31
    Superficial Atypical Melanocytic Proliferations of
    Uncertain Significance (SAMPUS and IAMPUS),
    Lentiginous Patterns 33
    2. Without Melanocytic Proliferation 34
    Atrophic Actinic Keratosis 34
    Porokeratosis 34
    C. Localized Lesions With Elongated Rete Ridges 36
    1. With Melanocytic Proliferation 36
    Actinic Lentigo 36
    Lentigo Simplex 37
    Lentiginous Junctional Nevus 37
    Nevus Spilus 38
    Junctional or Superficial Compound Dysplastic Nevi 40
    Nevoid Lentigo Maligna 42
    2. Without Melanocytic Proliferation 44
    Epidermal Nevus 44
    Seborrheic Keratoses 45
    Acanthosis Nigricans 45
    D. Localized Lesions With Pagetoid
    Epithelial Proliferation 47
    1. Keratinocytic Proliferations 47
    Pagetoid Squamous Cell Carcinoma In Situ (Bowen Disease) 47
    Clonal Seborrheic Keratosis 47
    2. Melanocytic Proliferation 48
    Melanoma In Situ or Microinvasive, Superficial
    Spreading Type 48
    Recurrent Nevus (Pseudomelanoma), Pagetoid Pattern 51
    Junctional Spitz Tumor (Nevus) With Pagetoid
    Proliferation 51
    Superficial/Intraepidermal Atypical Melanocytic
    Proliferations of Uncertain Significance
    (SAMPUS/IAMPUS), Pagetoid Patterns 51x Detailed Contents
    3. Glandular Epithelial Proliferations 54
    Paget Disease 54
    4. Lymphoid Proliferations 55
    Pagetoid Reticulosis (Woringer–Kolopp Disease) 55
    E. Localized Papillomatous Epithelial Lesions 55
    1. With Viral Cytopathic Effects 55
    Verruca Vulgaris 55
    Verruca Plana 55
    Deep Palmoplantar Warts (Myrmecia) 57
    Condyloma Acuminatum 57
    Molluscum Contagiosum 58
    Parapox Virus Infections (Milkers’ Nodules, Orf) 60
    2. No Viral Cytopathic Effect 61
    Seborrheic Keratosis 61
    Dowling–Degos Disease 61
    Confluent and Reticulated Papillomatosis
    (Gougerot–Carteaud) 62
    Verrucous Melanoma 64
    F . Irregular Proliferations Extending
    Into the Superficial Dermis 65
    1. Squamous Differentiation 65
    Inverted Follicular Keratosis 65
    2. Basaloid Differentiation 67
    Basal Cell Carcinoma 67
    G. Superficial Polypoid Lesions 69
    1. Melanocytic Lesions 69
    Polypoid Dermal and Compound Nevi 70
    2. Spindle Cell and Stromal Lesions 70
    Neurofibroma 71
    Fibroepithelial Polyp 71
    References 72
    Disorders of the Superficial
    Cutaneous Reactive Unit 77
    A. Superficial Perivascular Dermatitis 79
    1. Superficial Perivascular Dermatitis, Mostly Lymphocytes 79
    Viral Exanthem 79
    Pityriasis Versicolor 81
    Lupus Erythematosus, Acute 81
    Small Plaque Parapsoriasis (Guttate Parapsoriasis) 83
    1a. Superficial Perivascular Dermatitis With Eosinophils 84
    Morbilliform Drug Eruption 84
    Urticaria 84
    Urticarial Bullous Pemphigoid 87
    1b. Superficial Perivascular Dermatitis With Neutrophils 87
    Erysipelas 87
    Erysipelas/Cellulitis 87
    1c. Superficial Perivascular Dermatitis With Plasma Cells 88
    Secondary Syphilis 88
    Kaposi Sarcoma, Patch Stage 90
    III
    1d . S uper ficial P eriv asc ular D erma titis , W ith
    Extravasated Red Cells 92
    Pityriasis Rosea 92
    Pityriasis Lichenoides 93
    Pigmented Purpuric Dermatosis 95
    1e. Superficial Perivascular Dermatitis, Melanophages
    Prominent 97
    Postinflammatory Hyperpigmentation 97
    2. Superficial Perivascular Dermatitis, Mast
    Cells Predominant 98
    Urticaria Pigmentosa 98
    B. Superficial Dermatitis With Spongiosis
    (Spongiotic Dermatitis) 100
    Acute Spongiotic Dermatitis 100
    Subacute Spongiotic Dermatitis 100
    Chronic Spongiotic Dermatitis 100
    1. Spongiotic Dermatitis, Lymphocytes Predominant 101
    Nummular Dermatitis (Eczema) 101
    Meyerson Nevus 101
    1a. S pongiotic D erma titis , W ith E osinophils 103
    Allergic Contact Dermatitis 103
    Allergic Contact Dermatitis 104
    1b. Spongiotic Dermatitis, With Plasma Cells 106
    1c . S pongiotic D erma titis , W ith N eutr ophils 106
    Seborrheic Dermatitis 106
    C. S uper ficial Derma titis W ith Epidermal
    Atrophy (Atrophic Dermatitis) 107
    1. Atrophic Dermatitis, Scant Inflammatory Infiltrates 107
    Aged Skin 108
    Chronic Radiation Dermatitis 108
    2. Atrophic Dermatitis, Lymphocytes Predominant 108
    Poikiloderma Atrophicans Vasculare 108
    Dermatomyositis 110
    3. Atrophic Dermatitis With Papillary Dermal Sclerosis 111
    Lichen Sclerosus Et Atrophicus 111
    D. Superficial Dermatitis With Psoriasiform Proliferation
    (Psoriasiform Dermatitis) 113
    1. Psoriasiform Dermatitis, Mostly Lymphocytes 113
    Pityriasis Rubra Pilaris 113
    Mycosis Fungoides, Patch-Plaque Stage 113
    Parapsoriasis 117
    1a. P soriasif orm D erma titis , W ith Plasma C ells 118
    Lichen Simplex Chronicus (See also IIIE) 118
    1b . P soriasif orm D erma titis , W ith E osinophils 120
    Chronic Spongiotic Dermatitis 120
    2. Psoriasiform Dermatitis, Neutrophils Prominent
    (Neutrophilic/Pustular Psoriasiform Dermatitis) 120
    Psoriasis Vulgaris 120
    Guttate Psoriasis 121
    3. Psoriasiform Dermatitis, With Epidermal Pallor
    and Necrosis (“Nutritional Pattern” Dermatoses) 123
    Necrolytic Migratory Erythema (Glucagonoma Syndrome) 124
    Necrolytic Acral Erythema 125
    Pellagra 126Detailed Contents xi
    E. Superficial Dermatitis With Irregular Epidermal
    Proliferation (“Hypertrophic Dermatitis”) 128
    1. Hypertrophic Dermatitis, Lymphocytes Predominant 128
    Prurigo Nodularis 128
    1a. Irregular Epidermal Proliferation, Plasma
    Cells Present 129
    Actinic Keratosis (See also IIA1) 129
    2. Irregular Epidermal Proliferation,
    Neutrophils Prominent 130
    Keratoacanthoma (See also VIB1) 130
    Deep Fungus Infection (See also VD1) 130
    3. Irregular Epidermal Proliferation, Above A Neoplasm 130
    Verrucous Melanoma (See also VIB3) 130
    F . Superficial Dermatitis With Lichenoid
    Infiltrates (Lichenoid Dermatitis) 131
    1. Lichenoid Dermatitis, Lymphocytes Exclusively 131
    Lichen Planus 131
    Graft-Versus-Host Disease 133
    Mycosis Fungoides, Patch/Plaque Stage 134
    2. Lichenoid Dermatitis, Lymphocytes Predominant 135
    Lichen Planus–Like Keratosis (Benign
    Lichenoid Keratosis) 135
    2a. Lichenoid Dermatitis, Eosinophils Present 136
    Lichenoid Drug Eruptions 136
    2b. Lichenoid Dermatitis, Plasma Cells Present 138
    Lichenoid Actinic Keratosis 138
    Secondary Syphilis 138
    2c. Lichenoid Dermatitis, With Melanophages 139
    3. Lichenoid Dermatitis, Histiocytes Predominant 140
    Lichen Nitidus 140
    4. Lichenoid Dermatitis, Mast Cells Predominant 141
    Urticaria Pigmentosa, Lichenoid Examples 141
    5. Lichenoid Dermatitis With Dermal Fibroplasia 142
    Mycosis Fungoides, Patch Stage 142
    G. Superficial Vasculitis and Vasculopathies 143
    1. Neutrophilic Vasculitis 143
    Cutaneous Necrotizing (Leukocytoclastic) Vasculitis 144
    Septic Vasculitis (Gonococcemia) 145
    2. Mixed Cell and Granulomatous Vasculitis 146
    Granuloma Faciale 146
    3. Vasculopathies With Lymphocytic Inflammation 147
    Pigmented Purpuric Dermatoses 148
    4. Vasculopathies With Scant Inflammation 149
    Stasis Dermatitis 149
    Stasis Dermatitis 149
    5. Thrombotic, Embolic and Other Microangiopathies 150
    Lupus Anticoagulant and Antiocardiolipin Syndromes 150
    Cryoglobulinemia 151
    H. Superficial Dermatitis With Interface
    Vacuoles (Interface Dermatitis) 152
    1. Vacuolar Dermatitis, Apoptotic/Necrotic Cells Prominent 152
    Erythema Multiforme 152
    Fixed Drug Eruption 155
    Graft-Versus-Host Disease, Acute 155
    2. Vacuolar Dermatitis, Apoptotic Cells Usually Absent 156
    Dermatomyositis 156
    3. Vacuolar Dermatitis, Variable Apoptosis 157
    Subacute Cutaneous Lupus Erythematosus 157
    4. Vacuolar Dermatitis, Basement Membranes Thickened 159
    Discoid Lupus Erythematosus 159
    References 161
    Acantholytic, Vesicular, and
    Pustular Disorders 165
    A. Subcorneal or Intracorneal Separation 166
    1. Sub/Intracorneal Separation, Scant Inflammatory Cells 166
    Pemphigus Foliaceus 166
    2. Sub/Intracorneal Separation, Neutrophils Prominent 167
    Impetigo Contagiosa 167
    Staphylococcal Scalded Skin Syndrome 168
    Folliculitis With Subcorneal Pustule Formation 169
    Acute Generalized Exanthematous Pustulosis 169
    Pustular Psoriasis and Palmoplantar Pustulosis 170
    3. Sub/Intracorneal Separation, Eosinophils Predominant 173
    Erythema Toxicum Neonatorum 173
    Scabies With Eosinophilic Pustulosis 173
    B. Intraspinous Keratinocyte Separation, Spongiotic 174
    1. Intraspinous Spongiosis, Scant Inflammatory Cells 174
    Friction Blister 174
    2. Intraspinous Spongiosis, Lymphocytes Predominant 175
    Dyshidrotic Dermatitis/Eczema (Pompholyx) 176
    2a. Intraspinous Spongiosis, Eosinophils Present 176
    Acute Contact Dermatitis 177
    Bullous Pemphigoid, Urticarial Phase 178
    Incontinentia Pigmenti 178
    3. Intraspinous Spongiosis, Neutrophils Predominant 180
    Dermatophytosis 180
    C. Intraspinous Keratinocyte Separation,
    Acantholytic 181
    1. Intraspinous Acantholysis, Scant Inflammatory Cells 181
    Familial Benign Pemphigus (Hailey–Hailey Disease) 181
    Transient Acantholytic Dermatosis (Grover Disease) 182
    2. Intraspinous Acantholysis, Predominant Lymphocytes 184
    Herpes Simplex 184
    Varicella-Zoster Infection 187
    Toxic Epidermal Necrolysis, Stevens–Johnson
    Syndrome, and Erythema Multiforme
    With Intraepidermal Vesiculation 187
    Paraneoplastic Pemphigus 188
    2a. Intraspinous Acantholysis, Eosinophils Present 190
    Pemphigus Vegetans 190
    3. Intraspinous Separation, Neutrophils or
    Mixed Cell types 191
    IgA Pemphigus 191
    IVxii Detailed Contents
    D. Suprabasal Keratinocyte Separation 192
    1. Suprabasal Vesicles, Scant Inflammatory Cells 192
    Keratosis Follicularis (Darier Disease) 192
    Warty Dyskeratoma 194
    2. Suprabasal Separation, Lymphocytes and Plasma Cells 195
    Acantholytic Actinic Keratosis 195
    3. Suprabasal Vesicles, Lymphocytes and Eosinophils 195
    Pemphigus Vulgaris 195
    E . S ubepidermal V esic ular Derma titis 198
    1. Subepidermal Vesicles, Scant /No Inflammation 198
    Porphyria Cutanea T arda and Other Porphyrias 198
    2. Subepidermal Vesicles, Lymphocytes Predominant 200
    Bullous Lichen Planus 200
    Polymorphous (Polymorphic) Light Eruption 201
    Bullous Dermatophytosis 201
    Bullous Lichen Sclerosus et Atrophicus 203
    3. Subepidermal Vesicles, Eosinophils Prominent 204
    Bullous Pemphigoid 204
    Bullous Drug Eruption 204
    Pemphigoid Gestationis (Herpes Gestationis) 204
    4. Subepidermal Vesicles, Neutrophils Prominent 208
    Dermatitis Herpetiformis (Duhring Disease) 208
    Linear IgA Bullous Dermatosis 209
    Bullous Lupus Erythematosus 210
    Epidermolysis Bullosa Acquisita 211
    5. Subepidermal Vesicles, Mast Cells Prominent 213
    Bullous Mastocytosis 213
    References 214
    Perivascular, Diffuse, and
    Granulomatous Infiltrates
    of the Reticular Dermis 217
    A. Superficial and Deep Perivascular
    Infiltrates Without Vasculitis 219
    1. Perivascular Infiltrates, Lymphocytes Predominant 219
    Erythema Annulare Centrifugum 219
    Erythema Chronicum Migrans 219
    Tumid Lupus Erythematosus 219
    2. Perivascular Infiltrates, Neutrophils Predominant 222
    Cellulitis 222
    3. Perivascular Infiltrates, Lymphocytes and Eosinophils 223
    Papular Urticaria 223
    Urticaria 223
    Pruritic Urticarial Papules and Plaques of Pregnancy 224
    4. Perivascular Infiltrates, With Plasma Cells 226
    Secondary Syphilis 226
    Tertiary Syphilis 228
    Morphea (See Description in VF) 228
    5. Perivascular Infiltrates, Mixed Cell Types 230
    Erythema Chronicum Migrans 230
    V
    B. Vasculitis and Vasculopathies 231
    1. Vascular Damage, Scant Inflammatory Cells 231
    Degos Syndrome 231
    2. Vasculitis, Lymphocytes Predominant 232
    Pernio 232
    Pityriasis Lichenoides 232
    Cytomegalovirus Infection 235
    Erythema Chronicum Migrans 235
    3. Vasculitis, Neutrophils Prominent 236
    Polyarteritis Nodosa and Microscopic Polyangiitis 236
    Neutrophilic Small-Vessel Vasculitis
    (Leukocytoclastic Vasculitis) 237
    Erythema Elevatum Diutinum 239
    4. Vasculitis, Mixed Cell Types and/or Granulomas 240
    Eosinophilic Granulomatosis With Polyangiitis 240
    Papulonecrotic Tuberculid 240
    5. Thrombotic and Other Microangiopathies 242
    Calciphylaxis 242
    Livedo Reticularis 242
    C. Diffuse Infiltrates of the Reticular Dermis 243
    1. Diffuse Infiltrates, Lymphocytes Predominant 243
    Jessner Lymphocytic Infiltration of the Skin 243
    Leukemia Cutis 245
    2. Diffuse Infiltrates, Neutrophils Predominant 246
    Acute Febrile Neutrophilic Dermatosis (Sweet Syndrome) 246
    Neutrophilic Dermatosis of the Dorsal Hands 247
    Erysipelas 247
    3. Diffuse Infiltrates, “Histiocytoid” Cells Predominant 249
    Lepromatous Leprosy 249
    Langerhans Cell Histiocytosis (Histiocytosis X) 251
    Xanthelasma 253
    4. Diffuse Infiltrates, Plasma Cells Prominent 253
    Secondary Syphilis 253
    5. Diffuse Infiltrates, Mast Cells Predominant 254
    Urticaria Pigmentosa 254
    6. Diffuse Infiltrates, Eosinophils Predominant 255
    Eosinophilic Cellulitis (Wells Syndrome) 255
    Tick Bite 257
    7. Diffuse Infiltrates, Mixed Cell Types 258
    Cutaneous Leishmaniasis 258
    8. Diffuse Infiltrates, Pigment Cells 260
    Nevi of Ota and Ito and Dermal Melanocyte Hamartoma 260
    9. Diffuse Infiltrates, Extensive Necrosis 261
    Gangrenous Ischemic Necrosis 261
    D. Diffuse or Nodular Infiltrates of the Reticular
    Dermis With Epidermal Proliferation 262
    1. Epidermal Proliferation With Mixed Cellular Infiltrates 262
    North American Blastomycosis 262
    Deep Fungal Infections—General 264
    E. Nodular Inflammatory Infiltrates of the Reticular
    Dermis—Granulomas, Abscesses, and Ulcers 264
    1. Epithelioid Cell Granulomas Without Necrosis 264
    Sarcoidosis 265
    Lupus Vulgaris 266Detailed Contents xiii
    2. Epithelioid Cell Granulomas With Necrosis 267
    Tuberculosis 267
    Tuberculoid Leprosy 269
    Lupus Miliaris Disseminatus Facei 269
    3. Palisading Granulomas 270
    Granuloma Annulare 270
    Necrobiosis Lipoidica 272
    Necrobiotic Xanthogranuloma With Paraproteinemia 272
    Rheumatoid Nodules 272
    Palisaded Neutrophilic and Granulomatous Dermatitis 274
    4. Mixed Cell Granulomas 279
    Foreign-Body Reactions 279
    5. Inflammatory Nodules With Prominent Eosinophils 280
    Angiolymphoid Hyperplasia With Eosinophilia 280
    Epithelioid Hemangioma 280
    Kimura Disease 280
    Scabetic Nodule 281
    6. Inflammatory Nodules With Mixed Cell Types 283
    Sporotrichosis 283
    Atypical Mycobacteria 283
    7. Inflammatory Nodules With Necrosis and
    Neutrophils (Abscesses) 286
    Botryomycosis 287
    Chromoblastomycosis 288
    8. Inflammatory Nodules With Prominent Necrosis 288
    Aspergillosis 288
    9. Chronic Ulcers and Sinuses Involving the
    Reticular Dermis 290
    Chancroid 290
    Pyoderma Gangrenosum 291
    Chondrodermatitis Nodularis Helicis 293
    F . Dermal Matrix Fiber Disorders 293
    1. Fiber Disorders, Collagen Increased 293
    Scleroderma 293
    Radiation Dermatitis 294
    Nephrogenic Systemic Fibrosis 296
    Regressing Melanoma 298
    Superficial Scar (e.g., Biopsy Site Reaction) 300
    2. Fiber Disorders, Collagen Reduced 300
    Focal Dermal Hypoplasia (Goltz Syndrome) 300
    3. Fiber Disorders, Elastin Increased or Prominent 302
    Pseudoxanthoma Elasticum 302
    4. Fiber Disorders, Elastin Reduced 304
    Anetoderma (Macular Atrophy) 304
    5. Fiber Disorders, Perforating 304
    Elastosis Perforans Serpiginosa 304
    Reactive Perforating Collagenosis 305
    Perforating Folliculitis 305
    G. Deposition of Material in the Dermis 307
    1. Increased Normal Nonfibrous Matrix Constituents 307
    Digital Mucous Cysts and Cutaneous Focal Mucinosis 307
    Mucinosis in Lupus Erythematosus 307
    Mucinoses 307
    Pretibial Myxedema 308
    Scleredema 309
    Lichen Myxedematosus and Scleromyxedema 309
    2. Increased Material Not Normally Present in the Dermis 311
    Gout 311
    Oxalosis 313
    Colloid Milium 313
    Idiopathic Calcinosis Cutis 313
    Cryoglobulinemia 316
    Keratin Granuloma 316
    Suture Granuloma 317
    Minocycline Pigmentation 317
    3. Parasitic Infestations of the Dermis and/or Subcutis 318
    Cutaneous Larva Migrans 318
    References 319
    Tumors and Cysts of the
    Dermis and Subcutis 323
    A. Small and Intermediate Cell Tumors 325
    1. Tumors of Lymphocytes or Hemopoietic Cells 325
    Cutaneous B-Cell Follicle Center Lymphoma 325
    Cutaneous Diffuse B-Cell Lymphoma 327
    Primary Cutaneous Marginal Zone (MALT) Lymphoma 327
    Cutaneous T-Cell Lymphoma, Tumor Stage 327
    2. Tumors of Lymphocytes and Mixed Cell Types 330
    B-Cell Cutaneous Lymphoid Hyperplasia (B-CLH,
    Pseudolymphoma, Lymphocytoma Cutis) 330
    3. Tumors of Plasma Cells 331
    Cutaneous Plasmacytoma and Multiple Myeloma (MM) 331
    4. Small Round Cell Tumors 332
    Cutaneous Small Cell Undifferentiated Carcinoma
    (Merkel Cell Tumor) 333
    Metastatic Small Cell Carcinoma 333
    B. Large Polygonal and Round Cell Tumors 335
    1. Squamous Cell Tumors 335
    Squamous Cell Carcinoma 335
    Keratoacanthoma 336
    Inverted Follicular Keratosis 337
    Pseudoepitheliomatous Hyperplasia (PEH) 339
    Proliferating Trichilemmal Cyst (Pilar Tumor) 341
    Prurigo Nodularis 342
    2. Adenocarcinomas 343
    Metastatic Adenocarcinoma 343
    Metastatic Mammary Ductal Carcinoma 344
    Mammary Carcinoma, “Inflammatory” Type 344
    3. Melanocytic Tumors 346
    3a. Melanocytic Lesions With Little or No Cytologic Atypia 346
    Melanocytic Nevi, Acquired and Congenital Types 346
    Acquired Nevi, Compound and Dermal 347
    Balloon Cell Nevus 348
    Halo Nevus 348
    Acral Nevus 350
    Congenital Nevus 350
    Blue Nevus 350
    Cellular Blue Nevus 350
    VIxiv Detailed Contents
    3b. Melanocytic Lesions With Cytologic Atypia 354
    Deep Penetrating Nevus 354
    Spitz Tumor/Nevus 354
    Nodular Melanoma 356
    Superficial Spreading Melanoma (Tumorigenic) 358
    Nevoid Melanoma 359
    Metastatic Malignant Melanoma 359
    Metastatic Malignant Melanoma, Satellite Lesion 361
    Epidermotropic Metastatic Melanoma 361
    Pigmented Epithelioid Melanocytoma (PEM)/
    Epithelioid Blue Nevus 362
    Melanocytic Tumor of Uncertain Malignant Potential 363
    4. Eccrine Tumors 366
    4a. Circumscribed, Symmetrical Eccrine Tumors 366
    Eccrine Spiradenoma 366
    Cylindroma 368
    Poroma 369
    Syringoma 369
    Nodular Hidradenoma 370
    Clear Cell Syringoma 372
    Mixed Tumor (Chondroid Syringoma) 372
    4b. Infiltrative, Asymmetrical Eccrine Tumors 373
    Microcystic Adnexal Carcinoma 373
    Mucinous Carcinoma (Mucinous Eccrine Carcinoma) 374
    Digital Papillary Adenocarcinoma 374
    5. Apocrine Tumors 376
    Tubular Apocrine Adenoma 376
    Syringocystadenoma Papilliferum 376
    6. Pilar Tumors 379
    Trichoepithelioma 379
    Desmoplastic Trichoepithelioma 380
    Dilated Pore of Winer 381
    Pilar Sheath Acanthoma 381
    Trichilemmoma 382
    Trichofolliculoma 382
    Fibrofolliculoma/Trichodiscoma 382
    Trichoadenoma 382
    Pilomatricoma 385
    Trichoblastoma 385
    7. Sebaceous Tumors 387
    Sebaceous Adenoma and Sebaceous
    Epithelioma (Sebaceoma) 387
    Sebaceous Hyperplasia 388
    Nevus Sebaceus of Jadassohn 389
    Sebaceous Epithelioma 389
    Sebaceous Carcinoma 389
    8. “Histiocytoid” and Miscellaneous Clear Cell Tumors 391
    Xanthomas and Xanthelasma 391
    Xanthelasma 391
    Eruptive Xanthoma 391
    Verruciform Xanthoma 391
    Juvenile Xanthogranuloma (JXG) 394
    Reticulohistiocytosis 395
    Metastatic Renal Cell Carcinoma 395
    9. Tumors of Large Hematolymphoid Cells 397
    Cutaneous CD30+ (Ki-1+) Anaplastic
    Large Cell Lymphoma (ALCL) 397
    Lymphomatoid Papulosis 398
    Leukemia Cutis 399
    Primary Cutaneous Diffuse Large
    B-Cell Lymphoma, Leg Type 401
    10. Mast C ell T umors 403
    Urticaria Pigmentosa, Nodular Lesions (See also IIIA.2) 403
    11. Tumors With Prominent Necrosis 404
    Epithelioid Sarcoma 404
    12. Miscellaneous and Undifferentiated Epithelial Tumors 406
    Granular Cell Tumor 406
    Cellular Neurothekeoma 406
    Metastatic Malignant Melanoma 408
    C. Spindle Cell, Pleomorphic and Connective
    Tissue Tumors 409
    1. Fibrohistiocytic Spindle Cell Tumors 409
    1a. Fibrohistiocytic Tumors With Minimal or No Atypia 409
    Dermatofibroma 409
    Cellular Dermatofibroma 411
    Sclerosing/Angiomatoid Spitz Nevus
    (Desmoplastic Spitz Nevus) 411
    Dermatofibrosarcoma Protuberans 411
    Fibrous Papule (Angiofibroma) 414
    Recurrent Infantile Digital Fibromatosis 414
    Keloid 414
    Acquired Digital Fibrokeratoma 414
    Tenosynovial Giant Cell Tumor (Giant Cell
    Tumor of Tendon Sheath) 416
    Nodular Fasciitis 417
    1b. Fibrohistiocytic Tumors With High-Grade Atypia 418
    Atypical Fibroxanthoma 418
    Malignant Fibrous Histiocytoma (Pleomorphic Dermal
    Sarcoma) 419
    Dermatofibrosarcoma Protuberans With
    Sarcomatoid Change 420
    1c. Lesions With Myxoid Changes 421
    Mucocele 421
    Digital Mucous Cyst 421
    Cutaneous Myxoma 421
    2. Schwannian/Neural Spindle Cell Tumors 423
    Neurofibromas 423
    Neurofibromatosis 423
    Schwannoma (Neurilemmoma) 423
    Palisaded Encapsulated Neuroma 425
    Accessory Digit 427
    3. Spindle Cell Tumors of Muscle 429
    Leiomyomas 429
    Smooth Muscle Hamartoma 429
    Leiomyosarcoma 429
    4. Melanocytic Spindle Cell Tumors 433
    Desmoplastic Melanoma 433Detailed Contents xv
    5. Tumors and Proliferations of Angiogenic Cells 435
    Pyogenic Granuloma (Lobular Capillary Hemangioma) 435
    Intravascular Papillary Endothelial Hyperplasia
    (Masson’s Hemangioendotheliome
    Vegetant Intravasculaire) 436
    Stasis Dermatitis With Vascular Proliferation
    (Acroangiodermatitis, Pseudo-Kaposi Sarcoma) 437
    Kaposi Sarcoma 437
    Diffuse Dermal Angiomatosis 439
    Cutaneous Angiosarcoma 441
    Cutaneous Epithelioid Angiomatous Nodule/
    Epithelioid Hemangioendothelioma 443
    T argetoid Hemosiderotic Hemangioma
    (Hobnail Hemangioma) 443
    Angiokeratoma 445
    Arteriovenous Hemangioma 445
    Cavernous Hemangioma 445
    Cherry Hemangioma 447
    Microvenular Hemangioma 447
    Cutaneous Lymphangioma 447
    Venous Lake 447
    Glomangioma 447
    Glomus Tumor 447
    6. Tumors of Adipose Tissue 451
    Nevus Lipomatosus Superficialis 451
    Lipoma 451
    Angiolipoma 451
    Spindle Cell Lipoma 452
    Pleomorphic Lipoma 454
    Liposarcoma 454
    7. Tumors of Cartilaginous Tissue 455
    8. Tumors of Osseous Tissue 455
    Albright’s Hereditary Osteodystrophy and
    Osteoma Cutis 455
    D. Cysts of the Dermis and Subcutis 456
    1. Pilar Differentiation 456
    Epidermal or Infundibular Cyst 456
    Trichilemmal (Pilar) Cyst 457
    Steatocystoma 457
    Vellus Hair Cyst 457
    2. Eccrine and Similar Differentiation 459
    Eccrine Hidrocystoma 459
    Median Raphe Cyst 460
    Bronchogenic Cyst 460
    Cutaneous Endometriosis 460
    3. Apocrine Differentiation 462
    Apocrine Hidrocystoma 462
    Hidradenoma Papilliferum 462
    References 464
    Inflammatory and
    Other Disorders of Skin
    Appendages 469
    A. Pathology Involving Hair Follicles 470
    1. Scant Inflammation 470
    Androgenetic Alopecia 470
    Trichotillomania 470
    Telogen Effluvium 474
    Keratosis Pilaris 475
    Scurvy 475
    2. Lymphocytes Predominant 476
    Alopecia Areata 476
    Lichen Planopilaris 479
    Central Centrifugal Cicatricial Alopecia 480
    Discoid Lupus Erythematosus of the Scalp 480
    Follicular Mucinosis and Alopecia Mucinosa 480
    Rosacea 485
    3. With Prominent Eosinophils 487
    Eosinophilic Pustular Folliculitis 487
    4. Neutrophils Prominent 488
    Acute Deep Folliculitis (Furuncle) 488
    Tinea Capitis 488
    Majocchi Granuloma 488
    Herpes Simplex Viral Folliculitis 489
    5. Plasma Cells Prominent 491
    Folliculitis (Acne) Keloidalis Nuchae 491
    Tinea Capitis 492
    6. Fibrosing and Suppurative Follicular Disorders 493
    Follicular Occlusion Triad (Hidradenitis Suppurativa,
    Acne Conglobata, and Perifolliculitis Capitis
    Abscedens et Suffodiens) 493
    Hidradenitis Suppurativa 493
    Dissecting Cellulitis of the Scalp 495
    Folliculitis Decalvans 495
    B. Pathology Involving Sweat Glands 497
    1. Scant Inflammation 497
    Eccrine Nevus 498
    2. Lymphocytes Predominant 498
    Lichen Striatus 498
    2a. With Plasma Cells 499
    Lupus Erythematosus 499
    2b . W ith E osinophils 499
    Arthropod Assault Reaction 499
    2c. Neutrophils Predominant 500
    Neutrophilic Eccrine Hidradenitis 500
    Idiopathic Recurrent Palmoplantar Hidradenitis 500
    VIIxvi Detailed Contents
    C. Pathology Involving Nerves 502
    1. Lymphocytic Infiltrates 502
    2. Mixed Inflammatory Infiltrates 503
    Nerve Involvement in Leprosy 503
    Erythema Chronicum Migrans With Nerve Involvement 503
    Arthropod Bite Reaction With Nerve Involvement 503
    3. Neoplastic Infiltrates 504
    Neurotropic Melanoma 504
    D. Pathology of the Nails 505
    1. Lymphocytic Infiltrates 505
    Acral Lentiginous Melanoma 505
    2. Lymphocytes With Neutrophils 506
    Onychomycosis 506
    3. Vesiculobullous Diseases 507
    Darier Disease 507
    4. Parasitic Infestations 508
    Scabies 508
    References 508
    Disorders of the
    Subcutis 511
    A. Subcutaneous Vasculitis and Vasculopathy
    (Septal or Lobular) 512
    1. Neutrophilic Vasculitis 512
    Cutaneous/Subcutaneous Polyarteritis Nodosa
    (See also Section VB3 and T able VIII.1) 512
    2. Lymphocytic “Vasculitis” 513
    3. Granulomatous Vasculitis 513
    Erythema Induratum (Nodular Vasculitis) 513
    B. Septal Panniculitis Without Vasculitis 515
    1. Septal Panniculitis, Lymphocytes and Mixed Infiltrates 515
    Erythema Nodosum 515
    2. Septal Panniculitis, Granulomatous 517
    Subcutaneous Granuloma Annulare 517
    3. Septal Panniculitis, Sclerotic 519
    Scleroderma and Morphea 519
    C. Lobular Panniculitis Without Vasculitis 520
    1. Lobular Panniculitis, Lymphocytes Predominant 520
    Lupus Erythematosus Panniculitis 520
    VIII
    2. Lobular Panniculitis, Lymphocytes and
    Plasma Cells 522
    3. Lobular Panniculitis, Neutrophilic 522
    4. Lobular Panniculitis, Eosinophils Prominent 522
    5. Lobular Panniculitis, Histiocytes Prominent 522
    Cytophagic Histiocytic Panniculitis 522
    6. Lobular Panniculitis, Mixed With Foam Cells 524
    Relapsing Febrile Nodular Nonsuppurative Panniculitis 524
    7. Lobular Panniculitis, Granulomatous 526
    Subcutaneous Sarcoidosis 526
    8. Lobular Panniculitis, Crystal Deposits, Calcifications 526
    Subcutaneous Fat Necrosis of the Newborn 526
    Calcifying Panniculitis (Calciphylaxis) 528
    9. Lobular Panniculitis, Necrosis Prominent 529
    Subcutaneous Nodular Fat Necrosis in Pancreatic
    Disease 529
    10. Lobular Panniculitis, Embryonic Fat Pattern 531
    Localized Lipoatrophy and Lipodystrophy 531
    11. Lobular Panniculitis, Lipomembranous 532
    Lipomembranous Change or Lipomembranous
    Panniculitis 532
    D. Mixed Lobular and Septal Panniculitis 533
    1. With Hemorrhage or Sclerosis 533
    Panniculitis due to Physical or Chemical Agents 533
    2. With Many Neutrophils 534
    Necrotizing Fasciitis 534
    Alpha-1-Antitrypsin Deficiency–Associated Panniculitis 535
    3. With Many Eosinophils 536
    Eosinophilic Fasciitis (Shulman Syndrome) 536
    4. With Many Lymphocytes 538
    Subcutaneous Panniculitis-Like T-Cell Lymphoma 538
    5. With Cytophagic Histiocytes 539
    Sinus Histiocytosis With Massive Lymphadenopathy
    (SHML, Rosai–Dorfman) 539
    6. With Granulomas 540
    Mycobacterial Panniculitis 540
    Erythema Nodosum Leprosum (Type 2 Leprosy Reaction) 541
    E. Subcutaneous Abscesses 543
    1. With Neutrophils 543
    Phaeohyphomycotic Cyst 543
    References 544
    Index 547
    • Classifies patterns according to location, reaction patterns, and cell type if applicable, including diseases that have been recently described.
    • Color-codes each chapter for consistency, helping you navigate quickly to the information you need.
    • Compares “look-alike” diseases in easy-to-reference tables.
    • Includes multiple color photomicrographs for each disease, in addition to providing an online image bank.


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