Pytel Peter, Krausz Thomas, Wollmann Robert, Utset Manuel F
Department of Pathology, University of Chicago Hospitals, Chicago, IL 60637, USA.
Hum Pathol. 2005 Apr;36(4):444-6. doi: 10.1016/j.humpath.2005.01.024.
This study presents a rare case of compound paraganglioma/ganglioneuroma with comprehensive immunohistochemical studies that reveal strong cytokeratin expression in all components. A 74-year-old woman presented with a mass lesion of the cauda equina. The 1.8-cm tumor showed 3 histomorphologically and immunohistochemically distinct components: typical paragangliomatous neuroendocrine areas, mature ganglion cell-like neuronal areas, and a "neuromatous" proliferation of Schwann cells with admixed axons. As often seen in cauda equina paragangliomas, the neuroendocrine cells were cytokeratin-positive. In addition, immunoreactivity for cytokeratins was also observed in the neurons and axons. This tumor illustrates the broad spectrum of divergent differentiation that can be seen in cells of sympathoadrenal lineage.
本研究报告了一例罕见的复合性副神经节瘤/神经节神经瘤病例,并进行了全面的免疫组织化学研究,结果显示所有成分均有强烈的细胞角蛋白表达。一名74岁女性因马尾区肿块就诊。这个1.8厘米的肿瘤在组织形态学和免疫组织化学上显示出3种不同成分:典型的副神经节瘤样神经内分泌区域、成熟的神经节细胞样神经元区域,以及伴有混合轴突的雪旺细胞“神经瘤样”增殖。如马尾区副神经节瘤常见的那样,神经内分泌细胞呈细胞角蛋白阳性。此外,在神经元和轴突中也观察到细胞角蛋白的免疫反应性。该肿瘤说明了交感肾上腺谱系细胞中可见的广泛分化谱。