Literature DB >> 1893367

Endometrial carcinoma in the cancer family syndrome.

T Hakala1, J P Mecklin, M Forss, H Järvinen, P Lehtovirta.   

Abstract

The study group consisted of 26 women with endometrial adenocarcinoma belonging to 19 cancer families. Age at the onset of cancer, the stage and histologic differentiation of the tumor, initial symptoms, other malignancies, 5-year survival, and transmission of cancer to descendants were studied. The focus was on the importance of endometrial carcinoma in the tumor spectrum. The diagnosis of cancer family was delayed in 14 of the 19 families because endometrial carcinoma was not included in the primary diagnostic carcinoma. This delay may have been harmful to 16 family members who had carcinomas later in life. In ten of the 14 women with multiple malignancies, endometrial adenocarcinoma was the primary malignancy diagnosed, thus enabling the suspicion of a gene carrier and screening for subsequent malignancies. The authors concluded that endometrial carcinoma is a significant component of cancer family syndrome and should be included in the main criteria of Lynch syndrome II.

Entities:  

Mesh:

Year:  1991        PMID: 1893367     DOI: 10.1002/1097-0142(19911001)68:7<1656::aid-cncr2820680732>3.0.co;2-7

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


  6 in total

Review 1.  Molecular basis for subdividing hereditary colon cancer?

Authors:  W M Grady
Journal:  Gut       Date:  2005-12       Impact factor: 23.059

2.  Genetic implications of double primary cancers of the colorectum and endometrium.

Authors:  T Pal; T Flanders; M Mitchell-Lehman; A MacMillan; J S Brunet; S A Narod; W D Foulkes
Journal:  J Med Genet       Date:  1998-12       Impact factor: 6.318

3.  Linkage of a major breast cancer gene to chromosome 17q12-21: results from 15 Edinburgh families.

Authors:  B B Cohen; D E Porter; M R Wallace; A Carothers; C M Steel
Journal:  Am J Hum Genet       Date:  1993-04       Impact factor: 11.025

4.  Mismatch repair genes on chromosomes 2p and 3p account for a major share of hereditary nonpolyposis colorectal cancer families evaluable by linkage.

Authors:  M Nyström-Lahti; R Parsons; P Sistonen; L Pylkkänen; L A Aaltonen; F S Leach; S R Hamilton; P Watson; E Bronson; R Fusaro
Journal:  Am J Hum Genet       Date:  1994-10       Impact factor: 11.025

5.  Clinical features and mismatch repair gene mutation screening in Chinese patients with hereditary nonpolyposis colorectal carcinoma.

Authors:  Shan-Run Liu; Bo Zhao; Zhen-Jun Wang; Yuan-Lian Wan; Yan-Ting Huang
Journal:  World J Gastroenterol       Date:  2004-09-15       Impact factor: 5.742

6.  Other Gynecologic Cancers: endometrial, ovarian, vulvar and vaginal cancers.

Authors:  Eliane Duarte-Franco; Eduardo L Franco
Journal:  BMC Womens Health       Date:  2004-08-25       Impact factor: 2.809

  6 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.