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首页> 外文期刊>Pathology Research and Practice >Multiple sporadic gastrointestinal stromal tumors concomitant with ampullary adenocarcinoma: A case report with KIT and PDGFRA mutational analysis and miR-221/222 expression profile
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Multiple sporadic gastrointestinal stromal tumors concomitant with ampullary adenocarcinoma: A case report with KIT and PDGFRA mutational analysis and miR-221/222 expression profile

机译:多发性胃肠道间质瘤伴壶腹腺癌:1例KIT和PDGFRA突变分析及miR-221 / 222表达谱

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摘要

GISTs originating multifocally at different GI sites, in patients lacking familial syndromes, could be interpreted as recurrent/metastatic disease. MiR-221/222 have recently been identified as regulators of KIT expression in GISTs. We report the first case of synchronous GISTs in the stomach and duodenum concomitant with an ampullary adenocarcinoma. Different CD117 expression patterns could be related to different KIT mutational status in the two lesions: gastric GIST showed a dot-like pattern and lacked KIT mutations; duodenal GIST had a strong membranous expression pattern, likely due to KIT exon 9 duplication, which is associated with lower response to imatinib. MiR-221/222 were downregulated in GISTs as compared with normal tissue (p<. 0.05) and expressed increased levels in the gastric GIST as compared with duodenal one (p<. 0.05). Our data support an independent origin of the two GISTs. Determining whether these tumors are multiple primaries or recurrencies is helpful to predict their malignancy and to select proper treatment.
机译:在缺乏家族综合症的患者中,多灶性起源于不同GI位点的GIST可被解释为复发/转移性疾病。 MiR-221 / 222最近被确定为GIST中KIT表达的调节剂。我们报告在胃和十二指肠同时壶腹腺癌同步GISTs的第一例。在两种病变中,不同的CD117表达模式可能与不同的KIT突变状态有关:胃GIST呈点状模式且缺乏KIT突变;十二指肠GIST具有很强的膜表达模式,这可能是由于KIT外显子9重复引起的,这与对伊马替尼的反应较低有关。与正常组织相比,GIST中的MiR-221 / 222被下调(p <.0.05),与十二指肠之一相比,其胃GIST中的表达水平升高(p <.0.05)。我们的数据支持两个GIST的独立来源。确定这些肿瘤是多发性原发性还是复发性有助于预测其恶性程度并选择合适的治疗方法。

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