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Neurofibroma of the stomach without Recklinghausens disease: a case report

机译:无雷克林豪森氏病的胃神经纤维瘤:一例报告

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摘要

Neurofibromas of the stomach can occur in the course of Recklinghausen's disease. Sporadic gastric neurofibroma appears rarely. This tumour may look like an ulcer and can be a cause of abdominal pain, nausea, and bleeding from the gastrointestinal tract. We reported a 61-year-old women complaining of stomachache for several months. Gastroscopy revealed a tumour with ulceration in the prepyloric part of the stomach. Helicobacter pylori infection was also present. Helicobacter pylori eradication and prolonged treatment of proton pump inhibitors did not decrease the ailments or the size of the tumour. It was not possible to determine the nature and origin of the tumour by carrying out examinations such as endoscopic ultrasound and computed tomography of the abdomen. Only after surgery and histopathological examination with immunohistochemistry was this tumour identified as a neurofibroma. In order to differentiate the tumour the following immunohistochemical examinations were carried out: CD34 (slightly +), CD117 (–), S-100 (+), desmin (–), NSE (+), GFAP (–), SMA (–), bc12 (–), CD99 (–), ALK1 (–), and MiB (1–1.5%). In such cases excision of the tumour is the preferred treatment.
机译:胃神经纤维瘤可发生在雷克林豪森氏病的过程中。偶发性胃神经纤维瘤很少出现。该肿瘤看起来像溃疡,可能是引起腹痛,恶心和胃肠道出血的原因。我们报道了一名61岁的女性抱怨胃痛了几个月。胃镜检查发现肿瘤在胃的幽门前部有溃疡。还存在幽门螺杆菌感染。幽门螺杆菌的根除和质子泵抑制剂的长期治疗并未减少疾病或肿瘤的大小。通过进行诸如内窥镜超声检查和腹部计算机断层扫描等检查无法确定肿瘤的性质和起源。仅在手术和免疫组织化学组织病理学检查后,该肿瘤才被鉴定为神经纤维瘤。为了区分肿瘤,进行了以下免疫组化检查:CD34(轻微+),CD117(–),S-100(+),结蛋白(–),NSE(+),GFAP(–),SMA(– ),bc12(-),CD99(-),ALK1(-)和MiB(1-1.5%)。在这种情况下,切除肿瘤是首选的治疗方法。

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