Tan Guangming, Vitellas Kenneth, Morrison Carl, Frankel Wendy L
Departments of Pathology and Radiology, The Ohio State University Medical Center, Columbus, OH 43210, USA.
Ann Diagn Pathol. 2003 Oct;7(5):285-91. doi: 10.1016/s1092-9134(03)00082-0.
Intrapancreatic schwannoma is a rare neoplasm. We report a case of a 46-year-old man with a cystic schwannoma in the head of the pancreas. This tumor, based on clinical manifestations and radiologic features, was initially suspected to be a cystic mucinous tumor of the pancreas or a pseudocyst. Histologically, the tumor was a typical schwannoma with cyst formation caused by degenerative changes. Immunostaining showed the tumor cells to be strongly and diffusely positive for S-100 protein, vimentin, and CD56, and negative for cytokeratin AE1/AE3, desmin, smooth muscle myosin specific, CD34, and CD117, which support the diagnosis of schwannoma. Cystic schwannoma is a rare neoplasm occurring in the pancreas and should be considered in the differential diagnoses for patients presenting with pancreatic cystic lesions.
胰腺内神经鞘瘤是一种罕见的肿瘤。我们报告一例46岁男性,其胰腺头部患有囊性神经鞘瘤。基于临床表现和放射学特征,该肿瘤最初被怀疑为胰腺囊性黏液性肿瘤或假性囊肿。组织学上,该肿瘤是典型的神经鞘瘤,伴有因退行性变形成的囊肿。免疫组化显示肿瘤细胞对S-100蛋白、波形蛋白和CD56呈强阳性且弥漫性阳性,对细胞角蛋白AE1/AE3、结蛋白、平滑肌肌球蛋白特异性抗体、CD34和CD117呈阴性,这些结果支持神经鞘瘤的诊断。囊性神经鞘瘤是一种发生于胰腺的罕见肿瘤,对于出现胰腺囊性病变的患者,在鉴别诊断时应予以考虑。