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咖啡牛奶斑与早发性结直肠肿瘤:遗传性非息肉病性结直肠癌的一种变异型?

Café-au-lait spots and early onset colorectal neoplasia: a variant of HNPCC?

作者信息

Trimbath J D, Petersen G M, Erdman S H, Ferre M, Luce M C, Giardiello F M

机构信息

Department of medicine, The John Hopkins Hereditary Colorectal Cancer Registry, 550 N. Broadway, Suite 108, Baltimore, MD 21205-2011, USA.

出版信息

Fam Cancer. 2001;1(2):101-5. doi: 10.1023/a:1013881832014.

Abstract

BACKGROUND

Café-au-lait spots (CALS) are classically found in neurocutaneous syndromes such as neurofibromatosis, but have not been associated with hereditary colorectal cancer. However, review of hereditary colorectal cancer case reports reveals occasional description of CALS on physical exam.

METHODS

We describe the colonic and extracolonic phenotype in a family with CALS and early onset colorectal neoplasia (adenomas and/or cancer) and review 23 additional families reported in the literature.

RESULTS

Among the 24 families, 32/59 (54.2%) individuals had colorectal adenomas diagnosed at a mean age of 15.7 +/- 1.1 (SE) years (range 5-38 years). The majority (24/32, 75.0%) of persons at first colorectal examination had oligopolyposis (< 100 polyps) versus polyposis (> or = 100 polyps). Forty-two of 59 (71.2%) individuals were affected with colorectal cancer, diagnosed at a mean age of 31.9 +/- 2.7 years (range 5-70 years). A brain tumor was found in 28/59 (47.5%) affected individuals (4 families with 2 or more cases) with an overall mean age of diagnosis of 16.5 +/- 1.2. Lymphoma and/or leukemia was found in 8/24 (33.3%) families (one family with 3 cases). Two families had mutation of the mismatch repair gene, hPMS2 (1 with homozygous germline mutation), while two carried homozygous germline mutations of another mismatch repair gene, hMLH1.

CONCLUSIONS

Café-au-lait spots with early onset colorectal neoplasia may identify families with a variant of HNPCC characterized by oligopolyposis, glioblastoma at young age, and lymphoma. This variant may be caused by homozygous mutation of the mismatch repair genes, such as hPMS2 or hMLH1.

摘要

背景

咖啡牛奶斑(CALS)典型地见于神经皮肤综合征,如神经纤维瘤病,但尚未与遗传性结直肠癌相关联。然而,对遗传性结直肠癌病例报告的回顾显示,体格检查时偶尔会描述有咖啡牛奶斑。

方法

我们描述了一个患有咖啡牛奶斑和早发性结直肠肿瘤(腺瘤和/或癌)的家系的结肠和结肠外表型,并回顾了文献中另外报道的23个家系。

结果

在这24个家系中,59名个体中有32名(54.2%)被诊断患有结肠腺瘤,平均诊断年龄为15.7±1.1(标准误)岁(范围5 - 38岁)。初次结直肠检查时,大多数(24/32,75.0%)患者为寡息肉病(<100个息肉),而非息肉病(≥100个息肉)。59名个体中有42名(71.2%)被诊断患有结直肠癌,平均诊断年龄为31.9±2.7岁(范围5 - 70岁)。28/59(47.5%)名受影响个体(4个家系有2例或更多病例)发现患有脑肿瘤,总体平均诊断年龄为16.5±1.2岁。8/24(33.3%)个家系(1个家系有3例)发现患有淋巴瘤和/或白血病。两个家系的错配修复基因hPMS2发生突变(1个家系为纯合子种系突变),而另外两个家系携带另一种错配修复基因hMLH1的纯合子种系突变。

结论

伴有早发性结直肠肿瘤的咖啡牛奶斑可能识别出具有遗传性非息肉病性结直肠癌变异型的家系,其特征为寡息肉病、年轻时患胶质母细胞瘤和淋巴瘤。这种变异型可能由错配修复基因如hPMS2或hMLH1的纯合子突变引起。

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