Matsumoto H, Kojima Y, Inoue T, Takegawa S, Tsuda H, Kobayashi A, Watanabe K
Department of Surgery, Kanazawa National Hospital, Japan.
Surg Today. 1996;26(2):119-22. doi: 10.1007/BF00311775.
We report herein what to our knowledge is the first documented case of a malignant granular cell tumor of the stomach. A 64-year-old woman was admitted to our hospital for investigation of gastric submucosal tumor. Endoscopy disclosed a large hemispherical mass located on the lesser curvature at the gastric antrum with a normal mucosal surface, and computed tomography (CT) revealed a solid tumor about 7 cm in diameter with clear margins. A laparotomy was carried out under the preoperative diagnosis of leiomyosarcoma of the stomach. A tumor was found in the gastric antrum, with extragastric extension to the hepatic hilum, and a distal partial gastrectomy was performed. However, a follow-up CT scan performed 21 months postoperatively revealed a solid tumor of about 10 cm in diameter with clear margins, situated between the liver and the transverse colon. This was subsequently diagnosed as local recurrence and a resection was carried out. Microscopic examination of both the first and second specimens showed that the tumor cells were large and polygonal, with medullary proliferation and finely granular eosinophilic cytoplasm. Mitotic figures were also present. Thus, the lesion was diagnosed as a malignant granular cell tumor of the stomach from the clinical and pathological findings.
据我们所知,本文报告了首例有文献记载的胃恶性颗粒细胞瘤病例。一名64岁女性因胃黏膜下肿瘤入院接受检查。内镜检查发现胃窦小弯侧有一个大的半球形肿块,黏膜表面正常,计算机断层扫描(CT)显示一个直径约7厘米、边界清晰的实性肿瘤。术前诊断为胃平滑肌肉瘤,遂行剖腹手术。术中发现胃窦部有肿瘤,向肝门部胃外浸润,行远端胃部分切除术。然而,术后21个月的CT复查显示,在肝脏和横结肠之间有一个直径约10厘米、边界清晰的实性肿瘤。随后诊断为局部复发并进行了切除。对首次和第二次手术标本的显微镜检查显示,肿瘤细胞大且呈多边形,有髓样增生,细胞质呈细颗粒状嗜酸性。也有有丝分裂象。因此,根据临床和病理表现,该病变被诊断为胃恶性颗粒细胞瘤。