Watanabe Takayoshi, Araki Kenichiro, Ishii Norihiro, Igarashi Takamichi, Watanabe Akira, Kubo Norio, Kuwano Hiroyuki, Shirabe Ken
Department of Hepatobiliary and Pancreatic Surgery, Gunma University, Graduate School of Medicine, Gunma, Japan.
Integrative Center of General Surgery, Gunma University Hospital, Gunma, Japan.
Case Rep Gastroenterol. 2018 Feb 21;12(1):85-91. doi: 10.1159/000485559. eCollection 2018 Jan-Apr.
Pancreatic schwannomas are uncommon. About 60% of pancreatic schwannomas develop cystic lesions, and the differential diagnosis from other cystic pancreatic tumors is difficult. A 43-year-old man presented for evaluation of liver dysfunction detected during a medical checkup. Blood testing detected obstructive jaundice. A computed tomography scan revealed a well-defined polycystic tumor of about 5 cm at the pancreatic head. We performed surgical resection to treat the patient's symptoms and facilitate long-term management. Histopathological examination revealed spindle-shaped cells. Immunohistochemical studies showed S100 protein expression and the absence of CD34 and c-kit protein expression. Finally, we diagnosed a schwannoma. Pancreatic schwannoma is usually asymptomatic. The present case presented with obstructive jaundice, which is reportedly a rare symptom. Pancreatic schwannomas should be considered as a differential diagnosis of pancreatic cystic tumors. Dilatation of the pancreatic duct and the 18-fluorodeoxyglucose positron emission tomography findings are important for the differential diagnosis.
胰腺神经鞘瘤并不常见。约60%的胰腺神经鞘瘤会发展为囊性病变,与其他胰腺囊性肿瘤进行鉴别诊断较为困难。一名43岁男性因体检时发现肝功能异常前来评估。血液检测发现梗阻性黄疸。计算机断层扫描显示胰头有一个边界清晰的约5厘米的多囊性肿瘤。我们进行了手术切除以治疗患者症状并便于长期管理。组织病理学检查显示为梭形细胞。免疫组织化学研究显示S100蛋白表达阳性,且CD34和c-kit蛋白表达阴性。最终,我们诊断为神经鞘瘤。胰腺神经鞘瘤通常无症状。本病例表现为梗阻性黄疸,据报道这是一种罕见症状。胰腺神经鞘瘤应被视为胰腺囊性肿瘤的鉴别诊断之一。胰管扩张和18氟脱氧葡萄糖正电子发射断层扫描结果对鉴别诊断很重要。