A Case of Epidermolysis Bullosa Acquisita (Cicatricial pemphigoid-like type).
- Author:
Taek Hwan CHON
1
;
Soon Cheol KIM
;
Hong Yong KIM
;
Han Uk KIM
;
Chull Wan IHM
Author Information
1. Department of Dermatology, Chonbuk National University Medical School, Chonju, Korea.
- Publication Type:Case Report
- Keywords:
Epidermolysis bullosa acquisita;
Cicatricial pemphigoid-like type
- MeSH:
Aged;
Blister;
Epidermolysis Bullosa Acquisita*;
Epidermolysis Bullosa*;
Female;
Glycogen Storage Disease Type VI;
Humans;
Immunoglobulins;
Mucous Membrane
- From:Korean Journal of Dermatology
2000;38(6):793-797
- CountryRepublic of Korea
- Language:Korean
-
Abstract:
Epidermolysis bullosa acquisita (EBA) is an uncommon autoimmune subepidermal blistering disorder and has four clinical subtypes. Among the four types of EBA, the cicatricial pemphigoid-like type is rarer than the other types and clinically the worst one. We experienced a case of cicatricial pemphigoid-like type of EBA in a 69-year-old woman, whose initial symptom was painful erosive lesions of oral mucous membrane before development of ocular and bullous cutaneous lesions. The clinical, histopathological findings and immunoblot assay were all typical of the disease. The course of her disease showed remissions by treatments including corticosteroid and intravenous immunoglobulin, but each time with exacerbations.
