| Literature DB >> 21738978 |
Lívia do Nascimento Barbosa1, Roberto Souto da Silva, Gustavo Costa Verardino, Alexandre Carlos Gripp, Maria de Fátima Guimarães Scotelaro Alves.
Abstract
Mucous membrane pemphigoid (MMP) is a rare nosological entity. MMP consists of a clinical phenotype in which several autoimmune subepidermal bullous diseases are classified. It occurs predominantly in the mucous membranes and usually results in scarring. Esophageal involvement in MMP is rare and is generally seen in patients in whom lesions are widespread. The most common alterations are multiple esophageal membranes or strictures. In the present case, the authors report on a patient with MMP without any skin lesions and with severe esophageal strictures who went into remission following use of intravenous immunoglobulin.Entities:
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Year: 2011 PMID: 21738978 DOI: 10.1590/s0365-05962011000300023
Source DB: PubMed Journal: An Bras Dermatol ISSN: 0365-0596 Impact factor: 1.896