A case report of Muir-Torre syndrome in a woman with breast cancer and MSI-Low skin squamous cell carcinoma-Reference-Cited by-同舟云学术

A case report of Muir-Torre syndrome in a woman with breast cancer and MSI-Low skin squamous cell carcinoma

Published:2017-05-12 Issue:1 Volume:15 Page:
ISSN:1897-4287
Container-title:Hereditary Cancer in Clinical Practice
language:en
Short-container-title:Hered Cancer Clin Pract

Author:

Kientz Caroline,Joly Marie-Odile,Faivre Laurence,Clemenson Alix,Dalac Sophie,Lepage Côme,Chapusot Caroline,Jacquot Caroline,Schiappa Renaud,Lebrun Marine

Publisher

Springer Science and Business Media LLC

Subject

Genetics (clinical),Oncology

Link

http://link.springer.com/content/pdf/10.1186/s13053-017-0066-9.pdf

Reference17 articles.

1. Muir EG, Bell AJ, Barlow KA. Multiple primary carcinomata of the colon, duodenum, and larynx associated with kerato-acanthomata of the face. Br J Surg. 1967;54:191–5.

2. Torre D. Multiple sebaceous tumors. Arch Dermatol. 1968;98:549–51.

3. Arshad A, D’Angelis CA. Sebaceous tumors of the skin and Muir Torre Syndrome—a mini review. N A J Med Sci. 2014;7:87–92.

4. Umar A, Boland CR, Terdiman JP, Syngal S, de la Chapelle A, Rüschoff J, et al. Revised Bethesda guidelines for hereditary nonpolyposis colorectal cancer (Lynch syndrome) and microsatellite instability. J Natl Cancer Inst. 2004;96:261–8.

5. De la Chapelle A, Hampel H. Clinical relevance of microsatellite instability in colorectal cancer. J Clin Oncol. 2010;28:3380–7.

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