Oh Jung-Hwan, Jwa Seung-Joo, Yang Tae Ki, Lee Chang Sub, Oh Kyungmi, Kang Ji-Hoon
Department of Neurology, Jeju National University Hospital, Jeju 63241, Korea.
Department of Neurosurgery, Jeju National University Hospital, Jeju 63241, Korea.
Exp Neurobiol. 2015 Dec;24(4):366-70. doi: 10.5607/en.2015.24.4.366. Epub 2015 Dec 2.
Spontaneous spinal subdural hematoma (SDH) is very rare. Furthermore, intracranial vasospasm (ICVS) associated with spinal hemorrhage has been very rarely reported. We present an ICVS case without intracranial hemorrhage following SDH. A 41-year-old woman was admitted to our hospital with a complaint of severe headache. Multiple intracranial vasospasms were noted on a brain CT angiogram and transfemoral cerebral angiography. However, intracranial hemorrhage was not revealed by brain MRI or CT. On day 3 after admission, weakness of both legs and urinary incontinence developed. Spine MRI showed C7~T6 spinal cord compression due to hyperacute stage of SDH. After hematoma evacuation, her symptoms gradually improved. We suggest that spinal cord evaluation should be considered in patients with headache who have ICVS, although intracranial hemorrhage would not be visible in brain images.
自发性脊髓硬膜下血肿(SDH)非常罕见。此外,与脊髓出血相关的颅内血管痉挛(ICVS)鲜有报道。我们报告一例SDH后无颅内出血的ICVS病例。一名41岁女性因严重头痛入院。脑部CT血管造影和经股脑血管造影显示多处颅内血管痉挛。然而,脑部MRI或CT未发现颅内出血。入院第3天,患者出现双下肢无力和尿失禁。脊柱MRI显示由于SDH超急性期导致C7至T6脊髓受压。血肿清除术后,她的症状逐渐改善。我们建议,对于有ICVS的头痛患者,尽管脑部影像未显示颅内出血,也应考虑进行脊髓评估。