Soffer D, Pittaluga S, Caine Y, Feinsod M
Cancer. 1983 May 15;51(10):1907-10. doi: 10.1002/1097-0142(19830515)51:10<1907::aid-cncr2820511025>3.0.co;2-7.
A case of a cauda equina paraganglioma in a 13-year-old boy is described. A review of literature revealed six similar reported cases. All were intradural extramedullarly tumors located in the cauda equina-filum terminale region. In all, the presenting and dominant symptom was low back pain, while neurologic deficit was mild or absent. Excessive CSF protein levels appeared to be a characteristic feature of the disease. Histologically, the tumor displayed the typical "Zellballen" pattern, however mild nuclear pleomorphism and some mitotic figures were noted. As it is impossible to predict the biological behaviour of paragangliomas from the histologic appearance, complete surgical resection with close follow-up is indicated in such cases.
本文描述了一例13岁男孩马尾神经副神经节瘤的病例。文献回顾显示有6例类似的报道病例。所有病例均为硬膜内髓外肿瘤,位于马尾神经终丝区域。总体而言,主要症状为腰痛,而神经功能缺损轻微或无。脑脊液蛋白水平升高似乎是该疾病的一个特征性表现。组织学上,肿瘤呈现典型的“Zellballen”模式,但可见轻度核异形性和一些有丝分裂象。由于无法从组织学表现预测副神经节瘤的生物学行为,此类病例建议行完整手术切除并密切随访。