Gastric inflammatory fibroid polyp tumor with acute intestinal obstruction-Vanek's tumor can mimick a giant gastrointestinal stromal tumor or a gastric lymphoma.

Journal of visualized surgery Pub Date : 2018-03-16 eCollection Date: 2018-01-01 DOI:10.21037/jovs.2018.02.09
Francesco Fleres, Carmelo Mazzeo, Antonio Ieni, Maurizio Rossitto, Eugenio Cucinotta
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引用次数: 10

Abstract

An inflammatory fibroid polyp (IFP) is a solitary rare benign neoplasm of the gastrointestinal tract, frequently located in the gastric antrum. IFPs account for about 0.1% of all gastric polyps. We report a case of a giant gastric inflammatory polyp of 2.5 cm × 7 cm that determines a gastric outlet obstruction called "ball valve syndrome" mimicking a gastrointestinal stromal tumor (GIST) and a gastric lymphoma, with an intestinal obstruction of high origin. Therefore, due to acute presentation we have decided to submit the patient to a subtotal gastrectomy. The patient was discharged two weeks later, asymptomatic. At 14 months of follow-up, patient is disease free at abdominal CT and OGDS. Depending on their size and location, IFPs can be associated with unspecific symptoms. Giant IFPs of the gastric antrum or the duodenum can determine an intermittent gastric outlet obstruction called "ball valve syndrome". Endoscopic biopsies are unhelpful and right diagnosis can be reached only with resection. In fact, only about 10% of the gastric lesions are diagnosed correctly prior to resection. Surgical treatment with complete resection with safe margins is curative. Giant IFPs are rare benign lesions whose atypical presentation can mimic GISTs, lymphomas or carcinomas. Clinical and radiological findings may not clarify the right diagnosis until histopathological evaluation aided with immunohistochemical analysis. The resection of IFPs with negative margins is curative with a good clinical outcome. In acute presentation, like in our case, surgery is the mainstay of treatment.

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胃炎性肌瘤息肉合并急性肠梗阻- vanek肿瘤可以模拟巨大的胃肠道间质瘤或胃淋巴瘤。
炎性肌瘤息肉(IFP)是一种孤立的罕见的胃肠道良性肿瘤,通常位于胃窦。IFPs约占所有胃息肉的0.1%。我们报告一个2.5 cm × 7 cm的巨大胃炎性息肉,确定了胃出口梗阻,称为“球阀综合征”,模拟胃肠道间质瘤(GIST)和胃淋巴瘤,高来源的肠梗阻。因此,由于急性表现,我们决定提交病人胃大部切除术。两周后出院,无症状。随访14个月,腹部CT和OGDS均无病变。根据其大小和位置,ifp可能与非特异性症状有关。胃窦或十二指肠的巨大ifp可以确定间歇性胃出口梗阻,称为“球阀综合征”。内镜活检是没有帮助的,只有切除才能得到正确的诊断。事实上,只有约10%的胃病变在切除前被正确诊断。手术治疗与完全切除安全边缘是可治愈的。巨大的IFPs是罕见的良性病变,其不典型的表现可以模仿胃肠道间质瘤、淋巴瘤或癌。在组织病理学评估和免疫组织化学分析的辅助下,临床和影像学检查可能无法明确正确的诊断。切除边缘呈阴性的IFPs具有良好的疗效和临床效果。在急性表现中,像我们的病例,手术是主要的治疗方法。
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