Childhood epidermolysis bullosa acquisita: report of a Chinese case.

Abstract:

:Epidermolysis bullosa acquisita (EBA) is a rare, acquired, subepidermal blistering disease characterized by autoantibodies directed against type VII collagen, the major component of anchoring fibrils. We report a 5-year-old Chinese boy who presented with extensive lesions consisting of disseminated pruritic vesicles and tense blisters. The diagnosis of EBA was confirmed by histopathology, immunofluorescence, and immunoblotting analysis. The disease was controlled with a combination of prednisone and dapsone.

journal_name

Pediatr Dermatol

journal_title

Pediatric dermatology

authors

Yang B,Wang C,Wang N,Pan F,Chen S,Zhou G,Yu M,Zhang F

doi

10.1111/j.1525-1470.2011.01509.x

subject

Has Abstract

pub_date

2012-09-01 00:00:00

pages

614-7

issue

5

eissn

0736-8046

issn

1525-1470

journal_volume

29

pub_type

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