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Editorial
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Volume 354:293-295 January 19, 2006 Number 3
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Reducing the Risk of Gynecologic Cancer in the Lynch Syndrome
Kenneth Offit, M.D., M.P.H., and Noah D. Kauff, M.D.

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-Related Article
 by Schmeler, K. M.
-PubMed Citation
The first description of a kindred with hereditary nonpolyposis colorectal cancer (HNPCC) in 1925 was based on the family history of a woman who later died from endometrial cancer. On the basis of a detailed interview by Michigan pathologist Aldred Scott Warthin with this woman (his seamstress) and with other members of "Family G," Warthin described a large kindred with hereditary colorectal and endometrial cancers.1 Sixty-eight years later, Henry Lynch broadened the spectrum of hereditary cancers in the HNPCC syndrome to include ovarian cancer, transitional-cell cancer of the renal pelvis, and less often, stomach, small-intestine, pancreatic, and other types of . . . [Full Text of this Article]


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From the Memorial Sloan-Kettering Cancer Center, New York.


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