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[家族性腺瘤性结肠息肉病]

[Familial adenomatous colonic polyposis].

作者信息

Persić M, Kilvain S, Kapitanović S, Saina G, Roganović J, Rubinić M, Kovac D

机构信息

Klinika za djecje bolesti Kantrida, KBC Rijeka.

出版信息

Lijec Vjesn. 2000 May-Jun;122(5-6):132-5.

Abstract

We described two patients (brother and sister) with familial adenomatous polyposis of the colon. It is an inherited disease with autosomal dominant pattern of inheritance. The incidence is 1:8.000, with usual onset of polyps development late in the first decade of life or during adolescence, and malignant alteration up to the fourth decade of life. APC gene located on long arm of chromosome 5 is responsible for occurrence of the disease that presents with onset of multiple adenomatous polyps in the colon (from some of them to 1000). The treatment includes chemoprevention by sulindac or aspirin that prevents or reverse process of carcinogenesis. Surgical approach is preventive colectomy up to 20 (25) years of life. APC gene mutation (deletion at codon 1309-1311) was proven by DNA analysis from blood and polyp in both patients. There was no evidence of mutations of genes p53 and K-ras. Preventive colectomy is planned as soon as possible.

摘要

我们描述了两名患有家族性腺瘤性息肉病的患者(兄妹)。这是一种具有常染色体显性遗传模式的遗传性疾病。发病率为1:8000,息肉通常在生命的第一个十年后期或青春期开始出现,恶性病变可持续到生命的第四个十年。位于5号染色体长臂上的APC基因是导致该病发生的原因,该病表现为结肠内出现多个腺瘤性息肉(从几个到1000个不等)。治疗方法包括使用舒林酸或阿司匹林进行化学预防,以预防或逆转致癌过程。手术方法是在患者20(25)岁之前进行预防性结肠切除术。通过对两名患者血液和息肉的DNA分析,证实了APC基因突变(密码子1309 - 1311处缺失)。没有证据表明p53和K-ras基因发生突变。计划尽快进行预防性结肠切除术。

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