起源于胸椎的中枢神经系统浅表性铁沉着1例报告。

Korean Journal of Spine Pub Date : 2016-06-01 Epub Date: 2016-06-30 DOI:10.14245/kjs.2016.13.2.83
Sung Mo Ryu, Eun-Sang Kim, Seung-Kook Kim, Sun-Ho Lee, Whan Eoh
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引用次数: 7

摘要

摘要浅表性中枢神经系统黄素沉着症(SSCNS)是一种罕见的以含铁血黄素沉积在中枢神经系统表面为特征的疾病。我们报告一例起源于胸椎的SSCNS,表现为神经功能障碍,包括感觉神经性听力丧失,共济失调以及皮质脊髓和背柱束体征。患者接受人工硬脑膜修补。临床表现是通过神经学检查、影像学检查和术中发现得出的,这些都是通过文献回顾来解决的。
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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Superficial Siderosis of the Central Nervous System Originating from the Thoracic Spine: A Case Report.

Superficial siderosis of the central nervous system(SSCNS) is a rare disease characterized by hemosiderin deposition on the surface of the central nervous system. We report a case of SSCNS originating from the thoracic spine, presenting with neurological deficits including, sensorineuronal hearing loss, ataxia, and corticospinal and dorsal column tract signs. The patient underwent dural repair with an artificial dural patch. Clinical findings were elicited by neurological examination, imaging studies, and intraoperative findings, and these were addressed through literature review.

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