The cancer family syndrome. Rare cutaneous phenotypic linkage of Torre's syndrome
- 1 April 1981
- journal article
- research article
- Published by American Medical Association (AMA) in Archives of internal medicine (1960)
- Vol. 141 (5) , 607-611
- https://doi.org/10.1001/archinte.141.5.607
Abstract
Sebaceous neoplasia were observed in members of 4 families exhibiting the cancer family syndrome (CFS). This disorder is characterized by adenocarcinomas, particularly involving the (proximal) colon, endometrium and ovary; an excess of multiple primary cancer; early age of cancer onset; and autosomal dominant pattern of inheritance. Multiple adenomatous polyps are lacking in this disorder. In 4 patients from 3 of these cancer-prone kindreds, cutaneous lesions were accompanied by multiple visceral adenocarcinomas, fulfilling the criteria for Torre''s syndrome, a disease that heretofore has not shown notable familial clustering characteristic of the CFS. The coexistence of rare sebaceous neoplasia and visceral cancer in CFS supports the notion that some cases of Torre''s syndrome may represent the more full phenotypic expression of the gene responsible for the CFS.This publication has 10 references indexed in Scilit:
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