Gangliocytic paraganglioma of the cauda equina with significant calcification: first description in pediatric age.

M Vural, A Arslantas, S Isiksoy, B Adapinar, M Atasoy, F Soylemezoglu
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引用次数: 13

Abstract

A 17-year-old boy was referred with a 2-month history of low back pain and bilateral sciatica and difficulty in ambulation. Neurological examination found mild muscle weakness and diminished deep tendon reflexes in his right leg. Lumbar magnetic resonance imaging revealed an intradural-extramedullary tumor at the level of the L4, exiting through the right L4-L5 intervertebral foramen into the right psoas muscle. After total resection of the tumor, histopathological diagnosis revealed a gangliocytic paraganglioma. There are 184 paraganglioma cases reported at the lumbar region to date, and only 4 of them were in the pediatric age group. This report is the fifth paraganglioma case in the lumbar region and the first gangliocytic paraganglioma case in the pediatric age population.

伴有明显钙化的马尾神经节细胞副神经节瘤:首次在儿童时期描述。
一名17岁的男孩因2个月的腰痛和双侧坐骨神经痛以及行走困难而被转诊。神经学检查发现他的右腿有轻微的肌肉无力和深层肌腱反射减弱。腰椎磁共振成像显示在L4水平的硬膜内-髓外肿瘤,通过右侧L4- l5椎间孔进入右侧腰肌。肿瘤全切除后,病理组织诊断为神经节细胞副神经节瘤。迄今为止,有184例腰椎副神经节瘤病例报告,其中只有4例为儿童年龄组。本报告是第5例腰椎副神经节瘤病例和第一例神经节细胞副神经节瘤病例在儿童年龄人群。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Zentralblatt Fur Neurochirurgie
Zentralblatt Fur Neurochirurgie 医学-神经科学
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