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Familial adenomatous polyposis in China (Review).

Authors :
JUN YANG
QING WEI LIU
LIANG WEN LI
QIANG ZHI WANG
MIN HONG
JIAN DONG
Source :
Oncology Letters; Dec2016, Vol. 12 Issue 6, p4877-4882, 6p
Publication Year :
2016

Abstract

Familial adenomatous polyposis (FAP) is an autosomal dominant disease with a poor prognosis, and has been studied by clinicians and geneticists in China for the past three decades. It is estimated that FAP has an incidence of between 1 in 8,000 and 1 in 10,000 individuals, and accounts for 0.94% of colorectal cancer cases in China. Recent advances in the understanding of FAP suggest that the genotype of the patient may allow for early diagnosis and surveillance, and guide surgical and chemopreventive management. However, the genetic mechanisms of FAP vary between different countries. FAP in China has its own characteristics, and this may be due to ethnic and geographical genetic variation. In the present review the clinical manifestations and genetics of FAP in China are discussed, as well as the surgical strategies, chemotherapeutics and traditional Chinese medicines used in its treatment. Increased insight into the genetic and clinical features of FAP in the Chinese population may aid in the prevention and management of the disorder. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
17921074
Volume :
12
Issue :
6
Database :
Complementary Index
Journal :
Oncology Letters
Publication Type :
Academic Journal
Accession number :
119741418
Full Text :
https://doi.org/10.3892/ol.2016.5330