Terada Tadashi
Department of Pathology, Shizuoka City Shimizu Hospital, Miyakami 1231 Shimizu-Ku, Shizuoka 424-8636, Japan. Email:
Gastroenterology Res. 2009 Dec;2(6):364-366. doi: 10.4021/gr2009.01.1266. Epub 2009 Nov 20.
The author reports a typical but rare case of non-functioning well differentiated endocrine carcinoma of the pancreas. A 67-year-old man was admitted to our hospital because of abdominal pain. No hormone-related symptoms were recognized. He has no familiar history of pancreatic neoplasms. Various imaging modalities including US, CT and MRI revealed a tumor of the pancreatic body. Distal pancreatectomy and splenectomy were performed. A solid well demarcated tumor was present in the pancreatic body. Peripancreatic lymph nodes showed marked swelling suggestive of metastases. Immunohistyochemically, tumor cells were positive for cytokeratin, synaptophysin, neuron-specific enolase, and CD56; they were negative for chromogranin, gastrin, glucagon, somatostatin, pancreatic polypeptide, and vasoactive intestinal polypeptide. The pathological diagnosis was non-functioning well differentiated endocrine carcinoma of the pancreas.
作者报告了一例典型但罕见的胰腺无功能性高分化内分泌癌病例。一名67岁男性因腹痛入院。未发现激素相关症状。他没有胰腺肿瘤家族史。包括超声、CT和MRI在内的各种影像学检查显示胰体有肿瘤。行远端胰腺切除术和脾切除术。在胰体发现一个边界清晰的实性肿瘤。胰周淋巴结明显肿大提示转移。免疫组织化学检查显示,肿瘤细胞细胞角蛋白、突触素、神经元特异性烯醇化酶和CD56呈阳性;嗜铬粒蛋白、胃泌素、胰高血糖素、生长抑素、胰多肽和血管活性肠多肽呈阴性。病理诊断为胰腺无功能性高分化内分泌癌。