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以雷击样头痛为表现的自发性脊髓硬膜外血肿并自发恢复。

Thunderclap headache as a presentation of spontaneous spinal epidural hematoma with spontaneous recovery.

作者信息

Sathirapanya Pornchai, Setthawatcharawanich Suwanna, Limapichat Kitti, Phabphal Kanitpong

机构信息

Department of Internal Medicine, Faculty of Medicine, Prince of Songkla University, Hat Yai, Songkhla, Thailand.

出版信息

J Spinal Cord Med. 2013 Nov;36(6):707-10. doi: 10.1179/2045772313Y.0000000104. Epub 2013 Apr 13.

Abstract

BACKGROUND

Spontaneous spinal epidural hematoma (SSEH) is a rare spinal cord compression disorder. Thunderclap headache mimicking subarachnoid hemorrhage as an initial manifestation of this disorder has been scarcely reported. Moreover, the neurological outcome of conservative treatment is satisfactory only in some clinical settings. The unusual presentation and mechanisms for spontaneous recovery of SSEH are discussed.

OBJECTIVE

To report a case of SSEH that presented with acute severe headache that mimicked subarachnoid hemorrhage. After a period of neurological deficit, spontaneous improvement was seen, which progressed to full recovery without neurosurgical intervention.

FINDINGS

A 62-year-old man presented with acute occipital headache and neck stiffness for which subarachnoid hemorrhage was initially suspected. An emergency computed tomographic brain scan and cerebrospinal fluid analysis excluded subarachnoid hemorrhage. Later, he developed acute paraparesis, hypoesthesia up to the fourth thoracic dermatomal level (T4) as well as bowel and bladder dysfunction. The magnetic resonance imaging eventually revealed spinal epidural hematoma, located anterior to C7 through T4 spinal level. He had no previous history of spinal injury, systemic, and hematological disorders. The neurological recovery began 20 hours after the onset and continued until complete recovery, 4 months after the onset without neurosurgical intervention.

CONCLUSION

SSEH could sometimes imitate subarachnoid hemorrhages when it located in the cervical region. Spontaneous recovery of SSEH without surgical intervention might be possible in cases with continuing neurological recovery, although the recovery began much later in the clinical course.

摘要

背景

自发性脊髓硬膜外血肿(SSEH)是一种罕见的脊髓压迫性疾病。作为该疾病的初始表现,模仿蛛网膜下腔出血的霹雳样头痛鲜有报道。此外,保守治疗的神经学结果仅在某些临床情况下令人满意。本文讨论了SSEH不寻常的表现及自发恢复的机制。

目的

报告一例以模仿蛛网膜下腔出血的急性严重头痛为表现的SSEH病例。在出现一段时间的神经功能缺损后,病情出现自发改善,并在未进行神经外科干预的情况下完全恢复。

结果

一名62岁男性因急性枕部头痛和颈部僵硬就诊,最初怀疑为蛛网膜下腔出血。紧急脑部计算机断层扫描和脑脊液分析排除了蛛网膜下腔出血。随后,他出现急性截瘫、至第四胸皮节水平(T4)的感觉减退以及肠道和膀胱功能障碍。磁共振成像最终显示脊髓硬膜外血肿,位于C7至T4脊髓节段前方。他既往无脊髓损伤、全身性和血液系统疾病史。神经功能恢复在发病后20小时开始,并持续至发病后4个月完全恢复,未进行神经外科干预。

结论

当SSEH位于颈部时,有时可模仿蛛网膜下腔出血。对于神经功能持续恢复的病例,SSEH有可能在未进行手术干预的情况下自发恢复,尽管恢复在临床病程中开始得较晚。

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