Yoshida Hiroshi, Mamada Yasuhiro, Taniai Nobuhiko, Mizuguchi Yoshiaki, Nakamura Yoshiharu, Nomura Tsutomu, Okuda Takeshi, Uchida Eiji, Fukuda Yuh, Watanabe Manabu, Tajiri Takashi
Surgery for Organ Function and Biological Regulation, Graduate School of Medicine, Nippon Medical School, 1-1-5 Sendagi, Bunkyo-ku, Tokyo 113-8603, Japan.
J Nippon Med Sch. 2005 Oct;72(5):304-7. doi: 10.1272/jnms.72.304.
Calcifications within primary gastrointestinal tumors are rare. Gastrointestinal stromal tumor (GIST) is an unusual nonepithelial tumor that develops in the gastrointestinal tract. In this paper we describe a case of spurt bleeding from a calcificated GIST in the stomach successfully treated by partial gastric resection. A 77-year-old man was admitted for chest discomfort and loss of consciousness. Endoscopic examination revealed spurt bleeding from the top of the submucosal tumor. No other lesions or points of bleeding were found in the stomach. Emergency partial gastrectomy was performed, and the stomach was closed. The cut surface of the tumor had a firm, solid, whitish-gray parenchyma with patchy calcification. Microscopic observation revealed a profusion of spindle-shaped tumor cells with calcification growing from the gastric muscular propria to the submucosa. The cells exhibited low mitotic activity and no prominent signs of nuclear atypia. Immunohistochemical staining of the tumor demonstrated positive reactivity for CD34, KIT, and vimentin, but negative reactivity for alpha-smooth muscle actin, desmin, and S-100 protein. Tumor cells positive for Mib-1 were rare. The diagnosis of the tumor was established as GIST.
原发性胃肠道肿瘤内的钙化罕见。胃肠道间质瘤(GIST)是一种发生于胃肠道的非上皮性罕见肿瘤。本文描述了1例胃内钙化性GIST导致的喷射性出血,经胃部分切除成功治疗的病例。一名77岁男性因胸部不适和意识丧失入院。内镜检查显示黏膜下肿瘤顶部喷射性出血。胃内未发现其他病变或出血点。急诊行胃部分切除术,并关闭胃。肿瘤切面有坚实、实性、灰白色实质,伴有散在钙化。显微镜观察显示大量梭形肿瘤细胞伴钙化,从胃固有肌层向黏膜下层生长。细胞有低有丝分裂活性,无明显核异型性迹象。肿瘤的免疫组织化学染色显示CD34、KIT和波形蛋白呈阳性反应,但α-平滑肌肌动蛋白、结蛋白和S-100蛋白呈阴性反应。Mib-1阳性的肿瘤细胞罕见。肿瘤诊断为GIST。