In utero development of epidermolysis bullosa acquisita.


Journal

Pediatric dermatology
ISSN: 1525-1470
Titre abrégé: Pediatr Dermatol
Pays: United States
ID NLM: 8406799

Informations de publication

Date de publication:
Jan 2019
Historique:
pubmed: 20 10 2018
medline: 7 2 2019
entrez: 20 10 2018
Statut: ppublish

Résumé

We report the case of an infant born with perioral vesicles that rapidly spread to involve his mouth and the majority of his body. Histopathology, immunofluorescence, and enzyme-linked immunohistochemistry assays confirmed a diagnosis of epidermolysis bullosa acquisita (EBA). His mother had no history of EBA, and serum indirect immunofluorescence was negative. The patient improved rapidly with local wound care and oral dapsone.

Identifiants

pubmed: 30338555
doi: 10.1111/pde.13704
doi:

Substances chimiques

Folic Acid Antagonists 0
Dapsone 8W5C518302

Types de publication

Case Reports Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

e46-e47

Informations de copyright

© 2018 Wiley Periodicals, Inc.

Auteurs

Anna K Dewan (AK)

Department of Dermatology, Vanderbilt University Medical Center, Nashville, Tennessee.

Jonathan Braue (J)

Department of Dermatology, Vanderbilt University Medical Center, Nashville, Tennessee.

Brandon Danford (B)

Department of Dermatology, Vanderbilt University Medical Center, Nashville, Tennessee.

Lawrence B Stack (LB)

Department of Emergency Medicine, Vanderbilt University Medical Center, Nashville, Tennessee.

Alan S Boyd (AS)

Department of Dermatology, Vanderbilt University Medical Center, Nashville, Tennessee.

Jo-David Fine (JD)

Department of Dermatology, Vanderbilt University Medical Center, Nashville, Tennessee.

Sharon E Albers (SE)

Department of Dermatology, Vanderbilt University Medical Center, Nashville, Tennessee.

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Classifications MeSH