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结直肠癌患者中的林奇综合征

Lynch syndrome in colorectal cancer patients.

作者信息

Giráldez M Dolores, Castellví-Bel Sergi, Balaguer Francesc, Gonzalo Victòria, Ocaña Teresa, Castells Antoni

机构信息

Department of Gastroenterology, Institut de Malalties Digestives i Metabòliques, Hospital Clínic, CIBERehd, IDIBAPS, University of Barcelona, Barcelona, Catalonia, Spain.

出版信息

Expert Rev Anticancer Ther. 2008 Apr;8(4):573-83. doi: 10.1586/14737140.8.4.573.

Abstract

Lynch syndrome, also known as hereditary nonpolyposis colorectal cancer, is the most common form of hereditary colorectal cancer. It is characterized by early onset of colorectal cancer and other extracolonic-associated malignancies. This disorder is inherited in an autosomal dominant pattern and is due to a mutation in one of the DNA mismatch repair genes. Although clinical and molecular understanding of the syndrome has progressed dramatically in the last decade, diagnosis of the syndrome is still a clinical challenge. This review summarizes the main features of the syndrome and provides an update of its management.

摘要

林奇综合征,也称为遗传性非息肉病性结直肠癌,是遗传性结直肠癌最常见的形式。其特征是结直肠癌及其他结肠外相关恶性肿瘤发病较早。这种疾病以常染色体显性模式遗传,是由DNA错配修复基因之一发生突变所致。尽管在过去十年中对该综合征的临床和分子认识有了显著进展,但该综合征的诊断仍然是一项临床挑战。本综述总结了该综合征的主要特征,并提供了其治疗的最新情况。

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