Literature DB >> 12063922

[Muir-Torre syndrome].

J Jonas1, R Kruse, R Bähr.   

Abstract

The Muir-Torre syndrome (MTS) is an autosomal dominant disease defined by the coincidence of at least one sebaceous skin tumor and one internal malignancy. We describe an additional case and give a review of the literature. Over a period of 7 years, 19 skin tumors were excised in a 50 year old male patient. A total of 3 colonic carcinomas, one gastric carcinoma and one laryngeal carcinoma were operated successfully. The underlying defective mutation in the hMSH2 gene and the microsatellite instability were demonstrable. MTS is graded as a subgroup of hereditary non-polyposis colorectal cancer (HNPCC). In patients with MTS and with family members with known defective mutation, regular follow-up and search for new malignancies are mandatory.

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Year:  2002        PMID: 12063922     DOI: 10.1007/s00104-001-0392-2

Source DB:  PubMed          Journal:  Chirurg        ISSN: 0009-4722            Impact factor:   0.955


  2 in total

1.  [Suspected malignant gastric lesion in hereditary tumor syndrome: Endoscopic resection or gastrectomy?].

Authors:  M Kaths; I Gockel; P Kaudel; U Gönner; R Kiesslich; V Steinke; H Lang
Journal:  Chirurg       Date:  2013-07       Impact factor: 0.955

2.  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 in total

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