特发性自发性脊髓硬膜下血肿引起短暂性截瘫:1例报告并文献复习

Q Medicine

Neurosurgery Quarterly Pub Date : 2015-11-01 DOI:10.1097/WNQ.0000000000000092

Y. Oh, Jong-pil Eun

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引用次数: 3

摘要

自发性脊髓硬膜下血肿(SSDH)更为罕见，它可能发生在基础疾病包括肿瘤或动静脉畸形的凝血异常患者中。此外，自发性SSDH没有可检测到的结构病变或凝血功能障碍的病例极为罕见。我们经历了一个罕见的情况下，27岁的男子自发性急性SSDH无凝血功能障碍，谁提出了一过性截瘫。患者接受保守治疗后，神经系统症状完全恢复。为了讨论SSDH患者自发消退的可能机制，我们报告了我们的病例并回顾了文献。

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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Idiopathic Spontaneous Spinal Subdural Hematoma Causing Transient Paraparesis: Case Report With a Review of the Literature

Spontaneous spinal subdural hematoma (SSDH) is even rarer, and it may occur in patients with coagulation abnormalities whose underlying diseases include neoplasm or arteriovenous malformation. Moreover, there are extremely rare cases of spontaneous SSDH without detectable structural lesion or coagulopathy. We experienced a rare case of a 27-year-old man with spontaneous acute SSDH without coagulopathy who presented with transient paraparesis. The patient received a conservative treatment and then achieved a complete recovery of the neurologic symptoms. To discuss the possible mechanism of spontaneous resolution in patients with SSDH, we report our case with a review of the literature.

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来源期刊

Neurosurgery Quarterly 医学-神经科学

CiteScore

0.08

自引率

0.00%

发文量

审稿时长

6-12 weeks

期刊介绍： Neurosurgery Quarterly synthesizes the broad wealth of material on international developments in the diagnosis, management, and surgical treatment of neurological disorders. By encompassing viewpoints from worldwide sources, the journal provides information in greater depth than is usually found in the medical literature.