首页> 外文期刊>Familial cancer >A novel germline SDHB mutation in a gastrointestinal stromal tumor patient without bona fide features of the Carney-Stratakis dyad.
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A novel germline SDHB mutation in a gastrointestinal stromal tumor patient without bona fide features of the Carney-Stratakis dyad.

机译:胃肠道间质瘤患者中的新种系SDHB突变,无Carney-Stratakis家族的真正特征。

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摘要

Gastrointestinal stromal tumors (GISTs) are the most common mesenchyme neoplasms of the gastrointestinal tract. Gain-of-function somatic mutations of the KIT or PDGFRA genes represent the most prevalent molecular alterations in GISTs. In Carney-Stratakis dyad, patients portray germline mutations of the succinate dehydrogenase subunits B (SDHB), C (SDHC) and D (SDHD) and develop multifocal GISTs and multicentric paragangliomas (PGLs). We herein report a novel germline SDHB mutation (c.T282A--Ile44Asn) occurring in a 26 years-old patient diagnosed with a spindle cell intermediate risk GIST that did not present KIT/PDGFRA/BRAF gene mutations. Further analyses revealed loss of the wild-type SDHB allele and complete loss of SDHB expression in the tumor tissue. After genetic screening of other family members, we detected in the patient's mother a SDHB mutation without any clinical/laboratorial evidence of GIST or PGL. Altogether, our findings (germline SDHB mutation with absence of PGL in the index case and of GIST and/or PGL in his mother) raise the possibility that this familiar setting corresponds to an incomplete phenotype of the Carney-Stratakis dyad.
机译:胃肠道间质瘤(GIST)是胃肠道最常见的间质肿瘤。 KIT或PDGFRA基因的功能获得性体细胞突变代表了GIST中最普遍的分子改变。在卡尼-斯特拉塔基斯(Carney-Stratakis)二元组中,患者表现出琥珀酸脱氢酶亚基B(SDHB),C(SDHC)和D(SDHD)的种系突变,并发展出多灶性GIST和多中心副神经节瘤(PGL)。我们在这里报告了一种新的种系SDHB突变(c.T282A--Ile44Asn)发生在一名26岁的被诊断患有梭形细胞中度危险性GIST的患者中,该GIST不存在KIT / PDGFRA / BRAF基因突变。进一步的分析揭示了野生型SDHB等位基因的丧失和肿瘤组织中SDHB表达的完全丧失。在对其他家庭成员进行基因筛选后,我们在患者母亲中检测到SDHB突变,而没有任何GIST或PGL的临床/实验室证据。总而言之,我们的发现(索引病例中没有PGL,母亲中没有GIST和/或PGL的种系SDHB突变)增加了这种熟悉的情况对应于Carney-Stratakis家族不完整表型的可能性。

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