Abu-Zaid Ahmed, Azzam Ayman, Abou Al-Shaar Hussam, Alshammari Abdullah M, Amin Tarek, Mohammed Shamayel
College of Medicine, Alfaisal University, P.O. Box 50927, Riyadh 11533, Saudi Arabia ; Department of Surgical Oncology, King Faisal Specialist Hospital and Research Center (KFSH&RC), P.O. Box 3354, Riyadh 11211, Saudi Arabia.
Department of Surgical Oncology, King Faisal Specialist Hospital and Research Center (KFSH&RC), P.O. Box 3354, Riyadh 11211, Saudi Arabia ; Department of General Surgery, Faculty of Medicine, Alexandria University, Alexandria 21526, Egypt.
Case Rep Oncol Med. 2013;2013:416713. doi: 10.1155/2013/416713. Epub 2013 Nov 25.
Pancreatic schwannomas are exceedingly uncommon neoplasms. According to a recent study in 2012, less than 50 cases of pancreatic schwannoma have been described in the English literature over the past thirty years. The vast majority of pancreatic schwannomas take place in the head and body of pancreas, respectively. Herein, we report the case of pancreatic tail ancient schwannoma in a 44-year-old man who presented with a 4-month history of epigastric pain. On physical examination, epigastric region was moderately tender to palpation without evidence of a palpable mass. All laboratory tests were normal. Contrast-enhanced computed tomography (CT) scan showed a 9.2 × 9.5 × 11.5 cm, huge, and well-defined left suprarenal mass arising either from adrenal gland, pancreas, or retroperitoneum. The mass demonstrated mild heterogeneous enhancement with central cystic/necrotic area. No evidence of distant metastasis was identified. At laparoscopy, the mass was noticed to originate from pancreatic tail. Patient underwent surgical resection of pancreatic tail. Microscopic and immunohistochemical examination of the pancreatic tail specimen showed ancient schwannoma. Patient received no adjuvant therapy. At a postoperative 6-month followup, patient was completely asymptomatic and CT scan imaging showed no evidence of tumor recurrence. Moreover, a literature review on pancreatic schwannomas is presented.
胰腺神经鞘瘤是极其罕见的肿瘤。根据2012年的一项最新研究,在过去三十年里,英文文献中报道的胰腺神经鞘瘤病例不到50例。绝大多数胰腺神经鞘瘤分别发生在胰腺的头部和体部。在此,我们报告一例44岁男性胰腺尾部陈旧性神经鞘瘤的病例,该患者有4个月的上腹部疼痛病史。体格检查时,上腹部触诊有中度压痛,未触及肿块。所有实验室检查均正常。增强计算机断层扫描(CT)显示一个9.2×9.5×11.5厘米的巨大、边界清晰的左肾上腺肿块,可能起源于肾上腺、胰腺或腹膜后。肿块呈轻度不均匀强化,中央有囊性/坏死区。未发现远处转移的证据。在腹腔镜检查中,发现肿块起源于胰腺尾部。患者接受了胰腺尾部手术切除。对胰腺尾部标本进行显微镜和免疫组织化学检查显示为陈旧性神经鞘瘤。患者未接受辅助治疗。术后6个月随访时,患者完全无症状,CT扫描成像未显示肿瘤复发迹象。此外,还对胰腺神经鞘瘤进行了文献综述。