Kim Su Ho, Kim Jong Hyeok, Baik Gwang Ho, Baek Ilhyun, Hahn Taeho, Oh Soon Ok, Kim Jin Bong, Park Sang Hoon, Chang Woong Ki, Kim Dong Joon, Park Choong Kee, Park Hye Rim
Department of Internal Medicine, Hallym University College of Medicine, Chuncheon, Korea.
Korean J Gastroenterol. 2004 Jan;43(1):66-70.
GIST is a rare neoplasm, the majority of GISTs are located in the stomach and small intestine. Most GISTs are diagnosed histopathologically after resection because of submucosal location. A 37-year-old female patient presented with a 2-weeks history of generalized weakness, nausea accompanied by intermittent passage of black, tarry stools. Esophagogastroduodenoscopy and ERCP showed a large round mass measuring 5 cm in diameter in the ampulla of Vater with ulcer crack. Endoscopic multiple biopsies from the mass including ulcer base were taken. Light microscopic findings showed spindle-shaped and epitheloid tumor cells having high cellularity and frequent mitotic figures. On immunohistochemical stainings, the tumor cells were positive for CD34 and smooth muscle actin. Based on these preoperative findings, a diagnosis of malignant GIST of the ampulla of Vater was made probably. After operation, immunohistochemical studies revealed positive reaction for c-kit and vimentin, as well as focally reactive for CD34 and smooth muscle actin. We report a case of GIST in the ampulla of Vater presenting with melena that was diagnosed preoperatively and postoperatively.
胃肠道间质瘤(GIST)是一种罕见的肿瘤,大多数GIST位于胃和小肠。由于位于黏膜下层,大多数GIST在切除后经组织病理学诊断。一名37岁女性患者,有2周全身乏力、恶心伴间断排黑色柏油样便的病史。食管胃十二指肠镜检查和内镜逆行胰胆管造影(ERCP)显示在 Vater壶腹有一个直径5 cm的大圆形肿块,伴有溃疡破裂。从肿块包括溃疡底部取了内镜下多次活检。光镜检查结果显示梭形和上皮样肿瘤细胞,细胞密度高,有频繁的有丝分裂象。免疫组化染色显示肿瘤细胞CD34和平滑肌肌动蛋白呈阳性。基于这些术前检查结果,初步诊断为 Vater壶腹恶性GIST。术后免疫组化研究显示c-kit和波形蛋白呈阳性反应,CD34和平滑肌肌动蛋白呈局灶性反应。我们报告一例 Vater壶腹GIST患者,以黑便为表现,术前和术后均得以诊断。