A Case of Cap Polyposis Successfully Managed with Infliximab / 대한소화기내시경학회지
Korean Journal of Gastrointestinal Endoscopy
;
: 180-184, 2005.
Artigo
em Coreano
| WPRIM
| ID: wpr-175715
ABSTRACT
Cap polyposis is a rare disorder characterized by bloody, mucoid diarrhea with rectosigmoid polyps covered by a cap of fibrinopurulent exudate. The etiology and pathogenesis of cap polyposis is unknown, and no specific treatment has been established. Drug therapies are usually unsuccessful. Patients with a solitary cap polyp respond well to endoscopic polypectomy, while patients with multiple polyps and concurrent anorectal pathology require surgical resection. However, rapid recurrence has been described after a limited surgical resection, and this necessitates panproctocolectomy. We report a case of a 58-year-old female diagnosed as cap polyposis on rectum with similar clinical and endoscopic features of pseudomenbranous colitis successfully treated with infliximab (murine chimeric monoclonal antibody to TNF-alpha).
Texto completo:
DisponíveL
Índice:
WPRIM (Pacífico Ocidental)
Assunto principal:
Patologia
/
Pólipos
/
Reto
/
Recidiva
/
Enterocolite Pseudomembranosa
/
Colite
/
Diarreia
/
Tratamento Farmacológico
/
Exsudatos e Transudatos
/
Infliximab
Limite:
Feminino
/
Humanos
Idioma:
Coreano
Revista:
Korean Journal of Gastrointestinal Endoscopy
Ano de publicação:
2005
Tipo de documento:
Artigo
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