Pediatric dermatopathology / Thuy L. Phung, Teresa S. Wright, Crystal Y. Pourciau, Bruce R. Smoller.
This book provides practicing pathologists, dermatologists, cutaneous oncologists and dermatopathologists with a reference textbook that reviews the clinical and histopathologic features of skin disorders that affect children, along with a discussion of the molecular pathogenesis for each disease as...
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Full Text (via Springer) |
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| Main Authors: | , , , |
| Format: | eBook |
| Language: | English |
| Published: |
Cham, Switzerland :
Springer,
[2017]
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| Subjects: |
Table of Contents:
- Preface; Contributors; Contents; 1: Spongiotic Dermatitis; 1.1 Atopic Dermatitis; 1.1.1 Clinical Features; 1.1.2 Histology; 1.1.3 Pathogenesis; 1.2 Dyshidrotic Eczema; 1.2.1 Clinical Features; 1.2.2 Histology; 1.2.3 Pathogenesis; 1.3 Nummular Eczema; 1.3.1 Clinical Features; 1.3.2 Histology; 1.3.3 Pathogenesis; 1.4 Contact Dermatitis; 1.4.1 Clinical Features; 1.4.2 Histology; 1.4.3 Pathogenesis; 1.5 Autosensitization Dermatitis/Id Reaction; 1.5.1 Clinical Features; 1.5.2 Histology; 1.5.3 Pathogenesis; 1.6 Photoallergic Dermatitis; 1.6.1 Clinical Features.
- 1.6.2 Histology1.6.3 Pathogenesis; 1.7 Pityriasis Alba; 1.7.1 Clinical Features; 1.7.2 Histology; 1.8 Gianotti-Crosti Syndrome; 1.8.1 Clinical Features; 1.8.2 Histology; 1.8.3 Pathogenesis; 1.9 Intertrigo; 1.9.1 Clinical Features; 1.9.2 Histology; 1.9.3 Pathogenesis; 1.10 Periorificial Dermatitis; 1.10.1 Clinical Features; 1.10.2 Histology; 1.11 Juvenile Plantar Dermatosis; 1.11.1 Clinical Features; 1.11.2 Histology; 1.11.3 Pathogenesis; 1.12 Hyperimmunoglobulin E Syndrome; 1.12.1 Clinical Features; 1.12.2 Histology; 1.12.3 Pathogenesis; 1.13 Wiskott-Aldrich Syndrome.
- 1.13.1 Clinical Features1.13.2 Histology; 1.13.2.1 Pathogenesis; 1.14 Lichen Simplex Chronicus/Prurigo Nodularis; 1.14.1 Clinical Features; 1.14.2 Histology; 1.14.3 Pathogenesis; References; 2: Papulosquamous Diseases; 2.1 Ichthyosis Vulgaris; 2.1.1 Clinical Features; 2.1.2 Histology; 2.1.3 Pathogenesis; 2.2 Sex-Lined Ichthyosis; 2.2.1 Clinical Features; 2.2.2 Histology; 2.2.3 Pathogenesis; 2.3 Lamellar Ichthyosis; 2.3.1 Clinical Features; 2.3.2 Histology; 2.3.3 Pathogenesis; 2.4 Epidermolytic Hyperkeratosis/Bullous Congenital Ichthyosiform Erythroderma.
- 2.4.1 Clinical Features2.4.2 Histology; 2.4.3 Pathogenesis; 2.5 Non-bullous Epidermolytic Hyperkeratosis/Congenital Ichthyosiform Erythroderma; 2.5.1 Clinical Features; 2.5.2 Histology; 2.5.3 Pathogenesis; 2.6 Erythrokeratoderma Variabilis; 2.6.1 Clinical Features; 2.6.2 Histology; 2.6.3 Pathogenesis; 2.7 Netherton Syndrome; 2.7.1 Clinical Features; 2.7.2 Histology; 2.7.3 Pathogenesis; 2.8 Refsum Disease; 2.8.1 Clinical Features; 2.8.2 Histology; 2.8.3 Pathogenesis; 2.9 Sjogren-Larsson Syndrome; 2.9.1 Clinical Features; 2.9.2 Histology; 2.9.3 Pathogenesis.
- 2.10 Conradi-Hunermann-Happle Syndrome/X-Linked Dominant Chondrodysplasia Punctata Type 22.10.1 Clinical Features; 2.10.2 Histology; 2.10.3 Pathogenesis; 2.11 Other Syndromes with Ichthyosis; 2.12 Seborrheic Dermatitis; 2.12.1 Clinical Features; 2.12.2 Histology; 2.12.3 Pathogenesis; 2.13 Psoriasis; 2.13.1 Clinical Features; 2.13.2 Histology; 2.13.3 Pathogenesis; 2.14 Reactive Arthritis (Reiter's Disease); 2.14.1 Clinical Features; 2.14.2 Histology; 2.14.3 Pathogenesis; 2.15 Pityriasis Rubra Pilaris; 2.15.1 Clinical Features; 2.15.2 Histology; 2.15.3 Pathogenesis.