Large Intestinal Cancer
Copyright ©The Author(s) 2002. Published by Baishideng Publishing Group Inc. All rights reserved.
World J Gastroenterol. Oct 15, 2002; 8(5): 837-840
Published online Oct 15, 2002. doi: 10.3748/wjg.v8.i5.837
Analysis for phenotype of HNPCC in China
Yong-Mao Song, Shu Zheng
Yong-Mao Song, Department of Oncology, 2nd Affiliated Hospital, Medical College, Zhejiang University, Hangzhou 310009, Zhejiang Province, China
Shu Zheng, Cancer Institute, Zhejiang University, Hangzhou 310009, Zhejiang Province, China
Author contributions: All authors contributed equally to the work.
Correspondence to: Professor Shu Zheng, Cancer Institute, Zhejiang University, 88 Jiefang Road, Hangzhou 310009, Zhejiang Province, China. zsym@mail.hz.zj.cn
Telephone: +86-571-87214404 Fax: +86-571-87214404
Received: June 3, 2002
Revised: June 9, 2002
Accepted: June 12, 2002
Published online: October 15, 2002
Abstract

AIM: The aims of this study were to identify the clinicopathological features of Chinese HNPCC families and to evaluate the value of criteria for suspected HNPCC (sHNPCC) in clinical diagnosis.

METHODS: According to the follow-up records, 54 HNPCC families (including 12 ICG-HNPCC families and 42 sHNPCC families) were screened out from patients with colorectal cancers (CRCs), operated upon in 2nd Affiliated Hospital of Zhejiang University from 1984 to 2001. Clinical data of probands and tumor spectrum in these families were listed and analyzed.

RESULTS: (1) Mean age, proportion of colonic cancer, poorly differentiated cancer, multiple CRCs and Dukes’ A+B of the probands in ICG-HNPCC and sHNPCC kindred were 39 ys and 47.5 ys, 75% and 62%, 0 and 12.8%, 16.7% and 14.3%, 58.3% and 81%, respectively. Compared with sporadic colorectal cancers, probands from ICG-HNPCC and sHNPCC families were obviously different at age of onset (P = 0.025 and 0.031), tumor location (P = 0.001 and 0.000), differentiation (P = 0.002 and 0.011) and development of multiple tumors (P = 0.014 and 0.002). (2) A total of 178 malignant neoplasms were found in 54 HNPCC families, including 139 colorectal cancers. Besides of colorectal cancer, extracolonic tumors occurred in stomach, endometrium, hepatobiliary system, and so on (8 gastric cancers, 6 endometrial cancers, 6 hepatobiliary system cancers and 19 others) can also be seen in Chinese ICG-HNPCC and sHNPCC families.

CONCLUSION: (1) Chinese HNPCC families have specific clinicopathological features, such as early onset, predilection for the involvement of colon, tendency of multiple CRCs, development of extracolonic tumors and well differentiation. (2) The criteria for suspected HNPCC is useful in clinical diagnosis and management of HNPCC.

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