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脊髓硬膜下血肿源自颅内硬膜下血肿的迁移:两例报告及文献综述

Spinal Subdural Hematoma Migration From a Cranial Subdural Hematoma: Two Case Reports and Literature Review.

作者信息

Sakai Mamiko, Hotta Kensuke, Ikuta Ko, Nakashima Yasuharu

机构信息

Department of Orthopaedic Surgery, Kyushu Central Hospital, Fukuoka, JPN.

Department of Orthopaedic Surgery, Amagi Central Hspital, Asakura, JPN.

出版信息

Cureus. 2022 Jun 17;14(6):e26028. doi: 10.7759/cureus.26028. eCollection 2022 Jun.

Abstract

Spinal subdural hematoma (SSDH) associated with cranial subdural hematoma (CSDH) is considered extremely rare and the etiology remains unclear. Herein, we report two cases of spontaneous SSDH concomitant with CSDH, with no history of trauma. First, a healthy 35-year-old woman suffered from left leg pain following a headache caused by acute CSDH. Magnetic resonance imaging (MRI) of the lumbar spine showed SSDH extending from the L5 to S2 vertebral levels. The leg symptoms were gradually relieved with conservative treatments within two weeks after onset. The SSDH was completely resolved six months after onset on MRI evaluations. Next, a 69-year-old woman developed a headache and right hemiparesis. Brain computed tomography (CT) demonstrated chronic left-sided CSDH and she underwent a single burr-hole craniotomy. Three weeks after surgery, she experienced difficulty walking because of severe leg pain caused by SSDH extending from the L3 to S1. The clinical symptoms were completely resolved with conservative treatment within one month after onset. At 3 months follow-up, SSDH disappeared on MRI evaluation. Herein, we presented two cases of SSDH associated with CSDH. In both cases, the leg symptoms of SSDH developed following the onset of CSDH. Given that both patients remained active during the interval between CSDH onset and the appearance of SSDH symptoms, the SSDH was likely caused by migration of the CSDH contents to the lumbar spine because of gravity.

摘要

与颅骨硬膜下血肿(CSDH)相关的脊髓硬膜下血肿(SSDH)被认为极为罕见,其病因尚不清楚。在此,我们报告两例自发性SSDH合并CSDH的病例,患者均无外伤史。第一例,一名35岁健康女性因急性CSDH引起头痛后出现左腿疼痛。腰椎磁共振成像(MRI)显示SSDH从L5延伸至S2椎体水平。发病后两周内,经保守治疗腿部症状逐渐缓解。发病六个月后,MRI评估显示SSDH完全消退。第二例,一名69岁女性出现头痛和右侧偏瘫。脑部计算机断层扫描(CT)显示左侧慢性CSDH,她接受了单孔钻颅手术。术后三周,她因SSDH从L3延伸至S1导致严重腿痛而行走困难。发病后一个月内,经保守治疗临床症状完全缓解。随访3个月时,MRI评估显示SSDH消失。在此,我们展示了两例与CSDH相关的SSDH病例。在这两例中,SSDH的腿部症状均在CSDH发病后出现。鉴于两名患者在CSDH发病至SSDH症状出现的间隔期内仍活动自如,SSDH可能是由于CSDH内容物因重力作用向腰椎迁移所致。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6312/9288657/b966588189cf/cureus-0014-00000026028-i01.jpg

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