TURCOTS-SYNDROME AND FAMILIAL ADENOMATOUS POLYPOSIS ASSOCIATED WITH BRAIN-TUMOR - REVIEW OF RELATED LITERATURE

被引：39

作者：

ITOH, H

HIRATA, K

OHSATO, K

机构：

[1] Department of Surgery I, University of Occupational and Environmental Health, Kitakyushu

来源：

INTERNATIONAL JOURNAL OF COLORECTAL DISEASE | 1993年 / 8卷 / 02期

关键词：

D O I：

10.1007/BF00299334

中图分类号：

R57 [消化系及腹部疾病];

学科分类号：

摘要：

We investigated clinical manifestations in 124 patients with a possible Turcot's syndrome whose data were taken from documented cases. The cases were sub-classified mainly on the bases of the type of familial occurrence and listed in five Tables. We searched for differences in colonic manifestation, histologic type of glioma, mode of inheritance, frequency of parental consanguinity, skin lesions and other accompanying lesions among these five groups. The differences of these clinical findings suggested that glioma-polyposis syndrome should be classified as follows; (1) cases of Turcot's syndrome who had characteristic colonic and brain manifestations, (2) cases of FAP associated with glioma, (3) suspicious cases of glioma-polyposis, and (4) cases other than glioma-polyposis syndrome.

引用

页码：87 / 94

页数：8

共 77 条

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