Murata I, Makiyama K, Miyazaki K, Kawamoto A S, Yoshida N, Muta K, Itsuno M, Hara K, Nakagoe T, Tomita M
Second Department of Internal Medicine, Nagasaki University School of Medicine, Japan.
Gastroenterol Jpn. 1993 Aug;28(4):554-63. doi: 10.1007/BF02776955.
Primary malignant fibrous histiocytoma seldom occurs in the alimentary tract. This report documents a case in which a 50-year-old man presented with abdominal fullness and anorexia, together with inflammatory reactions such as fever, leukocytosis, an elevated erythrocyte sedimentation rate and positive CRP. Radiologic and endoscopic studies revealed a large mass in the ascending colon. The histology of the resected tumor revealed inflammatory malignant fibrous histiocytoma, a histologic subtype which is rare among not only soft tissue fibrous but also as gastrointestinal histiocytomas. The inflammatory reactions disappeared following resection of the tumor. Although we suspected that the tumor produced granulocyte colony-stimulating factor because of the slightly elevated serum level and the characteristics of the tumor histology, an immunohistochemical study failed to show the G-CSF production by the tumor cells.
原发性恶性纤维组织细胞瘤很少发生于消化道。本报告记录了一例病例,一名50岁男性出现腹部饱胀和厌食,同时伴有发热、白细胞增多、红细胞沉降率升高和C反应蛋白阳性等炎症反应。影像学和内镜检查显示升结肠有一个大肿块。切除肿瘤的组织学检查显示为炎症性恶性纤维组织细胞瘤,这种组织学亚型不仅在软组织纤维瘤中罕见,在胃肠道组织细胞瘤中也很少见。肿瘤切除后炎症反应消失。尽管由于血清水平略有升高和肿瘤组织学特征,我们怀疑肿瘤产生了粒细胞集落刺激因子,但免疫组化研究未能显示肿瘤细胞产生G-CSF。