胃肠道十二指肠间质瘤1例报告

A. Ghazanfar, Afifa Asghar, F. Zaman, H. Mumtaz, S. Habib, Shahzaib Ahmad 
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摘要

胃肠道间质瘤(GIST)是最常见的胃肠道间质肿瘤。它是由KIT和PDGFRα基因突变引起的。它占所有胃肠道肿瘤的不到1%。十二指肠胃肠道间质瘤占所有胃肠道间质瘤的4.5%。我们报告一位61岁的女士,在过去的3年里表现为全身腹痛,呕吐,腹胀和恶心。体格检查显示脸色苍白,腹部检查显示可触及的大肿块从骨盆延伸到腹部右上象限。CT扫描显示腹部和骨盆有一个大的不均匀回声肿块,该区域无淋巴结病变和远处转移。剖腹检查发现一个巨大的球状肿块,从骨盆延伸到腹部右上象限,附着在十二指肠的第三部分的壁上。用完整的包膜完成肿瘤的手术切除。镜下见肿瘤梭形细胞,肿瘤坏死。免疫组织化学研究证实GIST。
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A Case Presentation of Gastrointestinal Stromal Tumor of Duodenum
A gastrointestinal stromal tumor (GIST) is the most common mesenchymal tumor of the gastrointestinal tract. It is caused by the mutation in KIT and PDGFRα genes. It constitutes <1% of all gastrointestinal tumors. Duodenal GISTs constitute 4.5% of all GISTs. We report a 61-year-old lady, presented with generalized abdominal pain, vomiting, abdominal distension, and nausea for the last 3 years. Physical exam-ination showed a pallor and on abdominal examination, a large palpable mass was extending from the pelvis to the right upper quadrant of the abdomen. The CT scan showed a large heterogeneously echogenic mass in the abdomen and pelvis with no lymphadenopathy and distant metastasis in this region. Laparotomy showed a large globular mass extending from the pelvis to the right upper quadrant of the abdomen adherent to the wall of a third part of the duodenum. Complete surgical resection of tumor done with an intact capsule. Microscopic examination showed neoplastic spindle cells with tumor necrosis. An immunohistochemical study confirmed GIST.
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