Ide F, Shimoyama T, Horie N
Department of Oral Surgery, Saitama Medical Center, Saitama Medical School, Kawagoe, Japan.
J Oral Pathol Med. 1997 Mar;26(3):147-50. doi: 10.1111/j.1600-0714.1997.tb00039.x.
This report describes the morphologic and immunohistochemical features of two cases of glial choristoma arising in the palate. The bulk of the lesions consisted of mature neuroglial tissue admixed with salivary glands, adipose tissue and lymphoid aggregates in case 1 and of cartilage, bone and foci of smooth muscle cells in case 2. In addition, case 2 showed choroid plexus and melanin-containing epithelium. Neuroglial tissue was intensely positive for CD57 as well as for glial fibrillary acidic protein, S-100 protein and vimentin. Neuron-specific enolase and neurofilament were focally or weakly positive. Proliferating cell nuclear antigen was negative in case 1 but sparsely positive in case 2. These features reflect the fact that glial choristoma is a developmental malformation of heterotopic central nervous tissue with limited growth potential.
本报告描述了两例发生于腭部的神经胶质迷离瘤的形态学和免疫组化特征。病例1中,病变主要由成熟的神经胶质组织与唾液腺、脂肪组织和淋巴样聚集物混合组成;病例2中,病变由软骨、骨和平滑肌细胞灶组成。此外,病例2显示有脉络丛和含黑色素的上皮。神经胶质组织对CD57以及神经胶质纤维酸性蛋白、S-100蛋白和波形蛋白呈强阳性。神经元特异性烯醇化酶和神经丝呈局灶性或弱阳性。增殖细胞核抗原在病例1中为阴性,但在病例2中呈散在阳性。这些特征反映了神经胶质迷离瘤是一种具有有限生长潜能的异位中枢神经组织发育畸形这一事实。