Cho Min Young, Min Youn Ki, Kim Nam Ryeol, Cho Seong Jin, Kim Han Kyeom, Lee Kwang Chul, Suh Sung Ock, Whang Cheung Wung
Department of Surgery, College of Medicine Korea University, Seoul, Korea.
J Korean Med Sci. 2002 Oct;17(5):699-703. doi: 10.3346/jkms.2002.17.5.699.
Gastric inflammatory myofibroblastic tumor (IMT) is an extremely rare lesion with mimicking malignant features and accompanied with various clinical manifestations. Here we present a 2-yr-old boy who had a gastric IMT with a huge extragastric mass, which closely resembled a neuroblastoma on imaging studies. He experienced intermittent fever and poor appetite for 6 weeks. Fever remained up to 38 degrees C even on the operation day. He underwent partial gastrectomy and distal pancreatectomy with splenectomy including the tumor. The preoperative fever disappeared and did not recur in the postoperative course.
胃炎性肌纤维母细胞瘤(IMT)是一种极其罕见的病变,具有类似恶性的特征,并伴有各种临床表现。在此,我们报告一名2岁男孩,他患有胃IMT并伴有巨大的胃外肿块,影像学检查显示该肿块酷似神经母细胞瘤。他持续间歇性发热6周,食欲不佳。甚至在手术当天体温仍高达38摄氏度。他接受了包括肿瘤在内的胃部分切除术、远端胰腺切除术和脾切除术。术前发热消失,术后未再复发。