Shao-Yan Xu, Ying-Sheng Wu, Jian-Hui Li, Zhen-Hua Hu, Shu-Sen Zheng, Wei-Lin Wang, Division of Hepatobiliary and Pancreatic Surgery, Department of Surgery, First Affiliated Hospital, School of Medicine, Zhejiang University, Hangzhou 310003, Zhejiang Province, China.
World J Gastroenterol. 2017 May 28;23(20):3744-3751. doi: 10.3748/wjg.v23.i20.3744.
Schwannomas are neurogenic tumors that arise from the neural sheaths of peripheral nerves. These tumors can be located in any area of the human body; the most common locations are the head, neck, trunk and extremities. Pancreatic schwannomas are very rare. Over the past 40 years, only 67 cases of pancreatic schwannomas have been reported in the English literature. Here we present a case of pancreatic schwannoma in a 62-year-old male. The tumor was revealed by ultrasound and computed tomography in the neck and body of the pancreas. An accurate diagnosis was difficult to obtain preoperatively. The patient consented to the performance of a laparotomy, and the mass was found in the neck and body of the pancreas and successfully treated using a spleen-preserving distal pancreatectomy with splenic artery and vein preservation. The procedure has only been reported in one other case of pancreatic schwannoma; here we present the second reported case. Macroscopically, the tumor was well circumscribed, gray-white in color and 3.3 cm × 2.8 cm in size. Microscopically, the tumor cells were spindle-shaped and had a palisading arrangement with no atypia, which are results compatible with a benign tumor. Both hypercellular and hypocellular areas were visible. Immunohistochemically, the tumor cells were strongly positive for S-100 protein. The tumor was definitively diagnosed as a schwannoma of the pancreatic neck and body. The patient was followed for 72 mo and has been doing well without any complications.
神经鞘瘤是起源于周围神经神经鞘的神经源性肿瘤。这些肿瘤可以发生在人体的任何部位;最常见的部位是头部、颈部、躯干和四肢。胰腺神经鞘瘤非常罕见。在过去的 40 年中,英文文献中仅报道了 67 例胰腺神经鞘瘤。本文报道了 1 例 62 岁男性胰腺神经鞘瘤患者。肿瘤在颈部和胰腺体部通过超声和计算机断层扫描发现。术前很难获得准确的诊断。患者同意行剖腹探查术,在胰腺颈部和体部发现肿块,并成功采用保留脾脏的胰体尾切除术联合脾动静脉保留术进行治疗。该手术仅在另 1 例胰腺神经鞘瘤中报道;在此我们报道第 2 例。大体上,肿瘤边界清楚,灰白色,大小为 3.3cm×2.8cm。镜下,肿瘤细胞呈梭形,栅栏状排列,无异型性,符合良性肿瘤的结果。可见细胞丰富区和细胞稀少区。免疫组化染色,肿瘤细胞 S-100 蛋白阳性表达强。最终诊断为胰腺颈部和体部神经鞘瘤。患者随访 72 个月,情况良好,无任何并发症。