Inai K, Kobuke T, Yonehara S, Tokuoka S
Department of Pathology, Hiroshima University School of Medicine, Japan.
Cancer. 1989 Jun 15;63(12):2540-5. doi: 10.1002/1097-0142(19890615)63:12<2540::aid-cncr2820631231>3.0.co;2-h.
A case of duodenal gangliocytic paraganglioma (DGP) in a 17-year-old boy is presented. In this case a lymph node in the peripancreatic region was involved by a metastatic tumor. A review of the literature on DGP indicates that this case represents the youngest patient and is the second case of DGP with metastasis. Immunohistochemical staining for neuron-specific enolase (NSE), neurofilament (NF), pancreatic polypeptide, and somatostatin showed positive results for epithelioid and ganglion-like cells, whereas spindle cells showed immunoreactivities for S-100 protein, NSE, and NF. The histogenesis of DGP is discussed.
本文报道了一名17岁男孩患十二指肠神经节细胞性副神经节瘤(DGP)的病例。在该病例中,胰腺周围区域的一个淋巴结被转移性肿瘤累及。对DGP相关文献的回顾表明,该病例是最年轻的患者,也是第二例发生转移的DGP。神经元特异性烯醇化酶(NSE)、神经丝(NF)、胰多肽和生长抑素的免疫组织化学染色显示,上皮样细胞和神经节样细胞呈阳性结果,而梭形细胞对S-100蛋白、NSE和NF呈免疫反应性。文中讨论了DGP的组织发生。