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Medulloblastoma and Familial Adenomatous Polyposis in a 24-year-old Female Patient: A Case Report of Turcot Syndrome / 대한소아소화기영양학회지
Korean Journal of Pediatric Gastroenterology and Nutrition ; : 206-210, 2007.
Artigo em Coreano | WPRIM | ID: wpr-100255
ABSTRACT
Turcot syndrome is characterized by the concurrence of a primary neuroepithelial brain tumor and multiple colorectal polyposis. We report a case of a 24-year-old woman diagnosed with Turcot syndrome. At first, the patient was diagnosed as having a medulloblastoma after a tumorectomy of the 4th ventricle mass. The patient underwent radiotherapy and chemotherapy. After high-dose chemotherapy, neutropenic fever and severe mucositis developed. For an evaluation of the persistent hematochezia and diarrhea, a colonoscopy was performed. It revealed pseudomembranous colitis and multiple polyps in the entire colon. According to the family history, her father had undergone a total colectomy due to colon cancer and polyposis of the entire colon. Her brother also was found to have multiple polyps in the colon by a colonoscopy. The patient was diagnosed with Turcot syndrome.
Assuntos

Texto completo: DisponíveL Índice: WPRIM (Pacífico Ocidental) Assunto principal: Pólipos / Radioterapia / Neoplasias Encefálicas / Enterocolite Pseudomembranosa / Colonoscopia / Colectomia / Colo / Neoplasias do Colo / Polipose Adenomatosa do Colo / Irmãos Limite: Feminino / Humanos Idioma: Coreano Revista: Korean Journal of Pediatric Gastroenterology and Nutrition Ano de publicação: 2007 Tipo de documento: Artigo

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Texto completo: DisponíveL Índice: WPRIM (Pacífico Ocidental) Assunto principal: Pólipos / Radioterapia / Neoplasias Encefálicas / Enterocolite Pseudomembranosa / Colonoscopia / Colectomia / Colo / Neoplasias do Colo / Polipose Adenomatosa do Colo / Irmãos Limite: Feminino / Humanos Idioma: Coreano Revista: Korean Journal of Pediatric Gastroenterology and Nutrition Ano de publicação: 2007 Tipo de documento: Artigo