Guo Yun-Lei, Ruan Li-Tao, Wang Qiu-Ping, Lian Jie
Department of Ultrasound Medicine.
Department of Medical Imaging.
Medicine (Baltimore). 2018 Nov;97(48):e13516. doi: 10.1097/MD.0000000000013516.
Undifferentiated carcinoma with osteoclast-like giant cells (UC-OGCs) of the pancreas is an extremely rare and aggressive pancreatic malignancy. To our knowledge, the computed tomography (CT) findings of this disease have rarely been analyzed.
A 65-year-old man who experienced weight loss of about 4 kg over 3 months presented to our clinic. The abdominal ultrasound (US) detected a 5.8 × 5.5 cm well-defined, cystic-solid mass in the head of the pancreas, which had been present for 1 month.
A benign pancreatic tumor was initially suspected on the basis of the US findings. The patient then received serum tumor markers and CT examinations for further diagnosis, including carbohydrate antigen 199 (CA199), carcinoembryonic antigen (CEA), carbohydrate antigen 125 (CA125), contrast-enhanced CT (CECT) and CT angiography (CTA). His CA199, CEA, and CA125 marker levels were normal, which supported the diagnosis of a benign tumor. CECT showed a well-defined cystic-solid mass in the head of the pancreas, with a slightly enhanced solid portion and pancreatic ductal dilatation, which led us to consider the possibility of a malignant tumor. CTA revealed that the tumor nourishing arteries emitted from the pancreaticoduodenal superior and inferior arteries into the mass. Then, the patient underwent a pancreaticoduodenectomy. Finally, postoperative pathology and immunohistochemistry confirmed UC-OGC of the pancreas.
The patient has been treated by a pancreaticoduodenectomy alone.
The operation had no complications, and the patient recovered well after surgery. Ten months after surgery, the patient reviewed the CECT, and no recurrence or metastasis was noted.
Old patients with cystic-solid lesions in the pancreas should be aware of UC-OGC. CT findings usually show a clear boundary and a slightly enhanced mass with pancreatic duct expansion.
胰腺未分化癌伴破骨细胞样巨细胞(UC - OGC)是一种极其罕见且侵袭性强的胰腺恶性肿瘤。据我们所知,该病的计算机断层扫描(CT)表现很少被分析。
一名65岁男性,3个月内体重减轻约4千克,前来我院就诊。腹部超声(US)检查发现胰腺头部有一个5.8×5.5厘米边界清晰的囊实性肿块,已存在1个月。
根据超声检查结果,最初怀疑为良性胰腺肿瘤。患者随后接受了血清肿瘤标志物和CT检查以进一步诊断,包括糖类抗原199(CA199)、癌胚抗原(CEA)、糖类抗原125(CA125)、增强CT(CECT)和CT血管造影(CTA)。他的CA199、CEA和CA125标志物水平正常,这支持了良性肿瘤的诊断。CECT显示胰腺头部有一个边界清晰的囊实性肿块,实性部分轻度强化,伴有胰管扩张,这使我们考虑到恶性肿瘤的可能性。CTA显示肿瘤滋养动脉发自胰十二指肠上、下动脉并进入肿块。随后,患者接受了胰十二指肠切除术。最后,术后病理和免疫组化证实为胰腺UC - OGC。
患者仅接受了胰十二指肠切除术治疗。
手术无并发症,患者术后恢复良好。术后10个月,患者复查CECT,未发现复发或转移。
胰腺有囊实性病变的老年患者应警惕UC - OGC。CT表现通常显示边界清晰,肿块轻度强化伴胰管扩张。