Kishi Shinji, Monma Hiroyuki, Hori Hiroshige, Kinugasa Shoichi, Fujimoto Masayo, Nakamura Takeshi
Department of Surgery, Hyogo Prefectural Kakogawa Medical Center, Kakogawa, Hyogo, Japan.
Department of Surgery, Kobe Rosai Hospital, Kobe, Hyogo, Japan.
Am J Case Rep. 2018 Jun 5;19:642-650. doi: 10.12659/AJCR.909261.
BACKGROUND Giant cell tumor of soft tissue (GCT-ST) is a rare disease generally generated from superficial tissue. We report an extremely rare case of giant cell tumor of soft tissue arising from retroperitoneal tissue. CASE REPORT A 78-year-old man visited our medical center with the chief complaint of fatigue and weight loss for 1 month. He had a hard and immobilized mass without pain in the left upper quadrant. Contrast-enhanced CT showed a huge tumor (22×20×16 cm) in the retroperitoneal space, and it invaded into the stomach, colon, pancreas, spleen, and left kidney. MRI demonstrated the tumor had a serous cystic component as T1 was low, T2 was high, and DWI was slightly high. We diagnosed the retroperitoneal malignant tumor, and tumor resection was performed with total gastrectomy, partial colectomy, distal pancreatectomy, left nephrectomy, and left adrenalectomy for complete resection, without any postoperative complications. The tumor predominantly consisted of a solid mass, and had necrotic lesions, cystic lesions, and calcification. The histological exam showed it was composed of spindle and multinucleated giant cells; however, there was no cellular atypia or pleomorphism. Immunohistochemical staining characterized the tumor with CD68+, SMA+, CD34-, Desmin-, and S-100-. We finally diagnosed it as GCT-ST with the intermediate group of malignancy, according to WHO criteria. Thereafter, the patient had no recurrence at 1 year after resection. CONCLUSIONS The huge GCT-ST arising from the retroperitoneal space, which has never before been reported, was successfully resected. We report it with pathological findings to add to the relevant literature.
背景 软组织巨细胞瘤(GCT-ST)是一种罕见疾病,通常起源于浅表组织。我们报告一例极其罕见的起源于腹膜后组织的软组织巨细胞瘤病例。病例报告 一名78岁男性因1个月来疲劳和体重减轻为主诉前来我院就诊。他左上腹有一个坚硬、固定的肿块,无疼痛。增强CT显示腹膜后间隙有一个巨大肿瘤(22×20×16 cm),并侵犯胃、结肠、胰腺、脾脏和左肾。MRI显示肿瘤有一个浆液性囊性成分,T1低信号,T2高信号,DWI稍高信号。我们诊断为腹膜后恶性肿瘤,为完整切除行肿瘤切除术,包括全胃切除术、部分结肠切除术、远端胰腺切除术、左肾切除术和左肾上腺切除术,术后无任何并发症。肿瘤主要由实性肿块组成,有坏死灶、囊性灶和钙化。组织学检查显示其由梭形细胞和多核巨细胞组成;然而,无细胞异型性或多形性。免疫组化染色显示肿瘤CD68+、SMA+、CD34-、Desmin-、S-100-。根据WHO标准,我们最终诊断为中间恶性组的GCT-ST。此后,患者术后1年无复发。结论 起源于腹膜后间隙的巨大GCT-ST此前未见报道,已成功切除。我们报告此病例及病理结果以丰富相关文献。