An unusual case of Turcot's syndrome associated with ileal adenocarcinoma, intestinal non-Hodgkin's lymphoma, and duodenal adenocarcinoma. Review of the classification and genetic basis of Turcot's syndrome

被引:6
|
作者
Murphy, HR
Taylor, W
Ellis, A
Sturgess, R
机构
[1] Royal Liverpool Childrens Hosp, Dept Clin Genet, Liverpool L12 2AP, Merseyside, England
[2] Aintree Univ Hosp NHS Fdn Trust, Dept Pathol, Liverpool, Merseyside, England
[3] Royal Liverpool Univ Hosp, Dept Gastroenterol, Liverpool, Merseyside, England
[4] Aintree Univ Hosp NHS Fdn Trust, Dept Gastroenterol, Liverpool, Merseyside, England
关键词
colon cancer; duodenal cancer; family history; glioblastoma; non-Hodgkin's lymphoma; polyposis; Turcot's syndrome;
D O I
10.1007/s10689-004-2759-2
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
A 38-year-old man with a history of colonic and small bowel polyposis and glioblastoma was investigated for dyspepsia. Upper GI endoscopy identified an abnormal area in the duodenum, confirmed by histology as high grade non-Hodgkin's B cell MALT lymphoma. Although cases of Turcot's syndrome (TS) (colonic polyposis and primary brain tumour occuring in the same patient) have been previously described, association with haematological malignancy is rare. This is the first report of intestinal lymphoma occurring in an adult with TS.
引用
收藏
页码:139 / 143
页数:5
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