Concomitant Double Tumors of Myxopapillary Ependymoma Presented at Cauda Equina-Filum Terminale in Adult Patient.

Korean Journal of Spine Pub Date : 2016-03-01 Epub Date: 2016-03-31 DOI:10.14245/kjs.2016.13.1.33
Ulaş Yener, Mustafa Güdük, Murat Şakir Ekşi, Murat Hamit Aytar, Aydın Sav, Serdar Özgen
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引用次数: 10

Abstract

A 32-year-old man presented with gradually increasing bilateral buttock pain. He had intermittent claudication. Multiple, homogenously enhanced intradural extramedullary lesions at L2-L3 and L5-S1 levels were observed on magnetic resonance imaging. The tumors were debulked and were removed in piecemeal pattern until they had completely been resected. Histopathological examination of the surgical specimens confirmed that both tumors were myxopapillary ependymomas (MPE). MPE presenting as concomitant double tumor at conus-cauda-filum level are very rare. This kind of presentation could not be directly considered as dissemination, since both tumors were in the site of classical origin of MPE. Ten cases of double spinal MPEs have been reported to date. Including the present case, analysis of the 11 patients revealed some facts. There is a male predominance, which is opposite to the ependymomas that are commonly observed in females. Median age at presentation is 15 years. Most pronounced symptom is low back pain that sometimes radiates to lower extremities. Surgical approach was aimed in all tumors, which could be succeeded in all tumors except one. Adjuvant radiation therapy was applied in 5 patients. No recurrences have been reported after surgery or surgery + radiotherapy regimens.

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成人马尾-终丝状黏液乳头状室管膜瘤合并双瘤。
32岁男性,双侧臀部疼痛逐渐加重。他有间歇性跛行。磁共振成像在L2-L3和L5-S1水平观察到多发性均匀增强的硬膜内髓外病变。肿瘤被切除,并被分段切除,直到完全切除。手术标本的组织病理学检查证实两例肿瘤均为黏液乳头状室管膜瘤(MPE)。MPE表现为圆锥-尾-丝水平的双重肿瘤是非常罕见的。这种表现不能直接认为是播散,因为这两个肿瘤都在MPE的经典起源部位。迄今为止已报道了10例双脊柱MPEs病例。包括本病例在内,对11例患者的分析揭示了一些事实。男性多见,这与女性常见的室管膜瘤相反。发病年龄中位数为15岁。最明显的症状是腰痛,有时会扩散到下肢。手术入路对所有肿瘤均有效,除一例肿瘤外均可成功。辅助放射治疗5例。手术或手术+放疗方案后无复发报告。
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