Kawamoto Yusuke, Ome Yusuke, Terada Kazuhiro, Hashida Kazuki, Kawamoto Kazuyuki, Ito Tadashi
Department of Surgery, Kurashiki Central Hospital, Kurashiki, Okayama, Japan.
Department of Diagnostic Pathology, Kurashiki Central Hospital, Kurashiki, Okayama, Japan.
Int J Surg Case Rep. 2016;24:199-202. doi: 10.1016/j.ijscr.2016.04.057. Epub 2016 May 6.
Undifferentiated carcinomas with osteoclast-like giant cells (UC-OGCs) of the ampullary region are very rare, with only a few cases reported to date. The clinicopathological features, treatment options, and prognosis of UC-OGCs are unclear. This report describes a patient with UC-OGCs of the ampullary region.
A 78-year-old male patient was admitted for epigastric pain and fever. Contrast-enhanced computed tomography revealed a 2.6-cm mass at the duodenal papilla. Duodenoscopy revealed a smooth red protruding mass compressing the orifice of the papilla of Vater. Biopsy of the mass showed proliferation of osteoclast-like giant cells. A subtotal stomach-preserving pancreaticoduodenectomy was performed, and the tumor was histologically diagnosed as an UC-OGCs of the ampullary region. Carcinoma in situ was also observed, spreading from the tumor at the terminal segment of the common bile duct to the common hepatic duct, with carcinoma cells at the surgical margin of the common hepatic duct. One year after surgery, the patient is alive and without tumor recurrence.
UC-OGCs of the ampullary region is very rare neoplasm containing osteoclast-like giant cells and mononuclear cells. Osteoclast-like giant cells may originate from reactive mesenchymal cells and carcinoma in situ may spread to the common hepatic duct. Surgery including pancreaticoduodenectomy may be a treatment option for resectable tumors, whereas gemcitabine may be a treatment option for unresectable tumors.
Carcinoma in situ may spread quite far (5cm) to the common hepatic duct, making it desirable to intraoperatively confirm negative bile duct margins by rapid pathologic diagnosis.
壶腹区域具有破骨细胞样巨细胞的未分化癌(UC - OGCs)非常罕见,迄今为止仅有少数病例报道。UC - OGCs的临床病理特征、治疗选择和预后尚不清楚。本报告描述了一名患有壶腹区域UC - OGCs的患者。
一名78岁男性患者因上腹部疼痛和发热入院。增强计算机断层扫描显示十二指肠乳头处有一个2.6厘米的肿块。十二指肠镜检查发现一个光滑的红色突出肿块压迫 Vater 乳头开口。肿块活检显示破骨细胞样巨细胞增生。实施了保留胃的胰十二指肠次全切除术,肿瘤经组织学诊断为壶腹区域的UC - OGCs。还观察到原位癌,从胆总管末端的肿瘤蔓延至肝总管,肝总管手术切缘有癌细胞。术后一年,患者存活且无肿瘤复发。
壶腹区域的UC - OGCs是一种非常罕见的肿瘤,包含破骨细胞样巨细胞和单核细胞。破骨细胞样巨细胞可能起源于反应性间充质细胞,原位癌可能蔓延至肝总管。对于可切除的肿瘤,包括胰十二指肠切除术在内的手术可能是一种治疗选择,而吉西他滨可能是不可切除肿瘤的治疗选择。
原位癌可能向肝总管广泛蔓延(达5厘米),因此术中通过快速病理诊断确认胆管切缘阴性是可取的。