Pediatric Gastroenterology, Hepatology & Nutrition
- Volume 10 Issue 1
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- Pages.86-90
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- 2007
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- 2234-8646(pISSN)
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- 2234-8840(eISSN)
A Case of Rectal Carcinoid Tumor in a Child
소아 직장 유암종 1예
- Kang, Yo-Han (Department of Pediatrics, Sungmo Hospital) ;
- Son, Hyeon-Ee (Department of Pathology, Sungmo Hospital) ;
- Kim, Jae-Young (Department of Pediatrics, College of Medicine, Chungnam National University)
- Received : 2007.01.31
- Accepted : 2007.02.28
- Published : 2007.03.30
Abstract
Carcinoid tumors are derived from the enterochromaffin cells of neural crest origin. Most are commonly found in the gastrointestinal (GI) tract. The rectum is the third most common site for GI carcinoids. Rectal carcinoid tumors make up 13.7% of all carcinoid tumors and the vast majority occurs in the sixth decade of life. Approximately 80% of rectal carcinoid tumors are less than 1 cm in size, limited to the submucosa without metastasis and can be safely treated by local excision. We report a case of rectal carcinoid tumor in a 13 year-old child that was successfully treated by endoscopic polypectomy.
저자들은 내원 1년 전부터 간헐적인 복통과 함께 복통 시에 항상 동반되는 소량의 비특이적인 설사가 반복되어 내원한 13세 남아에서 직장 유암종을 진단하고 내시경적 절제술로 치료한 증례를 경험하였기에 문헌고찰과 함께 보고한다.