Literature DB >> 1544113

Phenotypic variation in hereditary nonpolyposis colon cancer syndrome. Association with infiltrative fibromatosis (desmoid tumor).

E R Maher1, B Morson, R Beach, S V Hodgson.   

Abstract

Familial infiltrative fibromatosis (desmoid tumor) is a recognized complication of familial adenomatous polyposis (FAP) but has not been described in families without colonic polyposis. The authors describe a unique family in which a predisposition to infiltrative fibromatosis and nonpolyposis colon cancer was inherited dominantly through four generations. This report expands the range of phenotypic variation described for the hereditary nonpolyposis colon cancer (HNPCC) syndrome and adds to the extracolonic complications that are common with FAP and HNPCC.

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Year:  1992        PMID: 1544113     DOI: 10.1002/1097-0142(19920415)69:8<2049::aid-cncr2820690807>3.0.co;2-6

Source DB:  PubMed          Journal:  Cancer        ISSN: 0008-543X            Impact factor:   6.860


  3 in total

1.  Analysis for phenotype of HNPCC in China.

Authors:  Yong-Mao Song; Shu Zheng
Journal:  World J Gastroenterol       Date:  2002-10       Impact factor: 5.742

2.  Hereditary desmoid disease due to a frameshift mutation at codon 1924 of the APC gene.

Authors:  D M Eccles; R van der Luijt; C Breukel; H Bullman; D Bunyan; A Fisher; J Barber; C du Boulay; J Primrose; J Burn; R Fodde
Journal:  Am J Hum Genet       Date:  1996-12       Impact factor: 11.025

3.  Extracolonic features of familial adenomatous polyposis in patients with sporadic colorectal cancer.

Authors:  M G Dunlop; S M Farrington; V J Bubb; C Cunningham; M Wright; L J Curtis; Z A Butt; E Wright; B W Fleck; D Redhead; R Mitchell; J B Rainey; I M Macintyre; D C Carter; A H Wyllie
Journal:  Br J Cancer       Date:  1996-12       Impact factor: 7.640

  3 in total

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