Taxy J B
Cancer. 1983 May 15;51(10):1904-6. doi: 10.1002/1097-0142(19830515)51:10<1904::aid-cncr2820511024>3.0.co;2-j.
The rare occurrence of a paraganglioma of the cauda equina is described. The correct diagnosis was made only retrospectively after examination of a recurrence nine years after initial surgery. Paragangliomas have not been mentioned in large tabulations of spinal cord tumors, perhaps reflecting the fact that it is only within the last decade that such tumors have been recognized in this unusual location. A literature review has revealed six cases of paraganglioma of the cauda equina reported since 1970. An awareness of the possibility of a paraganglioma intimately associated with the spinal cord as well as the histopathologic appearance are the bases of a correct diagnosis. These tumors are histopathologically similar to paragangliomas in conventional locations, exhibit ultrastructural granules and may, as in the current case, also demonstrate argyrophilic granules.
本文描述了一例罕见的马尾神经节细胞瘤。仅在初次手术后九年对复发情况进行检查后,才做出正确的回顾性诊断。在脊髓肿瘤的大型列表中未提及神经节细胞瘤,这可能反映出这样一个事实,即直到最近十年,才在这个不寻常的部位识别出此类肿瘤。文献综述显示,自1970年以来,已有6例马尾神经节细胞瘤的报道。认识到与脊髓密切相关的神经节细胞瘤的可能性以及其组织病理学表现是正确诊断的基础。这些肿瘤在组织病理学上与传统部位的神经节细胞瘤相似,具有超微结构颗粒,并且如本例所示,也可能显示嗜银颗粒。