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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.
Artículo en 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.
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Texto completo: Disponible Índice: WPRIM (Pacífico Occidental) Asunto principal: Pólipos / Radioterapia / Neoplasias Encefálicas / Enterocolitis Seudomembranosa / Colonoscopía / Colectomía / Colon / Neoplasias del Colon / Poliposis Adenomatosa del Colon / Hermanos Límite: Femenino / Humanos Idioma: Coreano Revista: Korean Journal of Pediatric Gastroenterology and Nutrition Año: 2007 Tipo del documento: Artículo

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Texto completo: Disponible Índice: WPRIM (Pacífico Occidental) Asunto principal: Pólipos / Radioterapia / Neoplasias Encefálicas / Enterocolitis Seudomembranosa / Colonoscopía / Colectomía / Colon / Neoplasias del Colon / Poliposis Adenomatosa del Colon / Hermanos Límite: Femenino / Humanos Idioma: Coreano Revista: Korean Journal of Pediatric Gastroenterology and Nutrition Año: 2007 Tipo del documento: Artículo