Pediatric dermatopathology. ([2017])
- Record Type:
- Book
- Title:
- Pediatric dermatopathology. ([2017])
- Main Title:
- Pediatric dermatopathology
- Further Information:
- Note: Thuy L. Phung, Teresa S. Wright, Crystal Y. Pourciau, Bruce R. Smoller.
- Authors:
- Phung, Thuy L
Wright, Teresa S
Pourciau, Crystal Y
Smoller, Bruce R - 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; 2.2.2Preface; 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. … (more)
- Publisher Details:
- Cham, Switzerland : Springer
- Publication Date:
- 2017
- Extent:
- 1 online resource
- Subjects:
- 618.92/5
Medicine
Pediatric dermatology
Skin -- Diseases
MEDICAL -- Gynecology & Obstetrics
Pediatric dermatology
Skin -- Diseases
Dermatology
Child
Medicine & Public Health
Pathology
Dermatology
Surgical Oncology
Medical -- Dermatology
Medical -- Surgery -- General
Dermatology
Surgical oncology
Pathology
Dermatology
Surgical oncology
Medical -- Pathology
Pathology
Electronic books - Languages:
- English
- ISBNs:
- 9783319448244
3319448242 - Related ISBNs:
- 9783319448220
3319448226 - Notes:
- Note: Includes bibliographical references and index.
Note: Online resource; title from PDF title page (EBSCO, viewed June 27, 2017). - Access Rights:
- Legal Deposit; Only available on premises controlled by the deposit library and to one user at any one time; The Legal Deposit Libraries (Non-Print Works) Regulations (UK).
- Access Usage:
- Restricted: Printing from this resource is governed by The Legal Deposit Libraries (Non-Print Works) Regulations (UK) and UK copyright law currently in force.
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- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library HMNTS - ELD.DS.363868
- Ingest File:
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