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A case of pemphigus vulgaris associated with ulcerative colitis
Intestinal Research ; : 147-150, 2018.
Artículo en Inglés | WPRIM | ID: wpr-740012
ABSTRACT
Pemphigus vulgaris is an autoimmune bullous disorder characterized by the production of autoantibodies against the intercellular space of the epithelium. It has rarely been reported in association with inflammatory bowel disease. Ulcerative colitis is one of the forms of inflammatory bowel disease. A 62-year-old woman who had been treated for ulcerative colitis for 16 years developed pruritic bullae on the skin of her face and body. Histological findings and direct immunofluorescence examination of the skin showed pemphigus vulgaris. She was treated with systemic steroids, mesalazine, and azathioprine. Her cutaneous lesions have remained in remission and her ulcerative colitis has remained well-controlled. The relationship between pemphigus vulgaris and ulcerative colitis is unclear. An autoimmune response has been suspected in the pathogenesis of ulcerative colitis. Pemphigus vulgaris is also associated with an autoimmune mechanism. To our knowledge, this is the first case of ulcerative colitis associated with pemphigus vulgaris reported in Korea. The association may be causal.
Asunto(s)

Texto completo: Disponible Índice: WPRIM (Pacífico Occidental) Asunto principal: Piel / Autoanticuerpos / Esteroides / Azatioprina / Úlcera / Enfermedades Inflamatorias del Intestino / Colitis Ulcerosa / Autoinmunidad / Pénfigo / Técnica del Anticuerpo Fluorescente Directa Límite: Femenino / Humanos País/Región como asunto: Asia Idioma: Inglés Revista: Intestinal Research Año: 2018 Tipo del documento: Artículo

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Texto completo: Disponible Índice: WPRIM (Pacífico Occidental) Asunto principal: Piel / Autoanticuerpos / Esteroides / Azatioprina / Úlcera / Enfermedades Inflamatorias del Intestino / Colitis Ulcerosa / Autoinmunidad / Pénfigo / Técnica del Anticuerpo Fluorescente Directa Límite: Femenino / Humanos País/Región como asunto: Asia Idioma: Inglés Revista: Intestinal Research Año: 2018 Tipo del documento: Artículo