Inflammatory epidermolysis bullosa acquisita - Case report

dc.creatorFERNANDES, Marcelo D`Ambrosio
dc.creatorCHIMINAZZO, Mariana Discacciati
dc.creatorTEBCHERANI, Antonio Jose
dc.creatorAOKI, Valeria
dc.creatorSANCHEZ, Ana Paula Galli
dc.date.accessioned2012-10-19T17:22:17Z
dc.date.accessioned2018-07-04T15:06:54Z
dc.date.available2012-10-19T17:22:17Z
dc.date.available2018-07-04T15:06:54Z
dc.date.created2012-10-19T17:22:17Z
dc.date.issued2009
dc.identifierANAIS BRASILEIROS DE DERMATOLOGIA, v.84, n.2, p.181-184, 2009
dc.identifier0365-0596
dc.identifierhttp://producao.usp.br/handle/BDPI/21998
dc.identifierhttp://apps.isiknowledge.com/InboundService.do?Func=Frame&product=WOS&action=retrieve&SrcApp=EndNote&UT=000265985800012&Init=Yes&SrcAuth=ResearchSoft&mode=FullRecord
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/1618771
dc.description.abstractWe report a case of an inflammatory variant of epidermolysis bullosa acquisita in a 53-year-old male, with itching blistering eruption on the trunk, armpits and limbs for six months. The skin biopsy specimen showed subepidermal blister with neutrophils. Direct immunofluorescence revealed linear depositions of IgG, IgA, IgM and C3 at the basement membrane; indirect immunofluorescence and salt split skin were negative. Antinuclear antibodies were also negative. Improvement of the blisters followed treatment with systemic corticotherapy and some lesions healed with milia. This is a rare presentation of epidermolysis bullosa acquisita, with inflammatory lesions at first.
dc.languagepor
dc.publisherSOC BRASILEIRA DERMATOLOGIA
dc.relationAnais Brasileiros de Dermatologia
dc.rightsCopyright SOC BRASILEIRA DERMATOLOGIA
dc.rightsclosedAccess
dc.subjectBasement membrane
dc.subjectBlister
dc.subjectEpidermolysis bullosa acquisita
dc.titleInflammatory epidermolysis bullosa acquisita - Case report
dc.typeArtículos de revistas


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