Yamada K, Nakahara T, Yamamato K, Muranaka T, Ushio Y
Department of Neurosurgery, Kumamoto University Medical School, Kumamoto, Japan.
Acta Neurochir (Wien). 2003 Feb;145(2):151-5; discussion 155. doi: 10.1007/s00701-002-1045-z.
Spontaneous occurrence of spinal subdural haematoma (SSH) is very rare. While many neurological disorders can develop in pregnant patients in relation to haemostatic imbalance, there have been no reports in the literature suggesting that pregnancy and/or childbirth per se could be a single risk factor for acute SSH.A 38-year-old previously healthy woman gave birth to a baby via transvaginal normal delivery. The patient had no history of receiving anticoagulants. Eight days after delivery, she experienced sudden onset severe interscapular back pain, and the next day she developed dysesthesia in the both legs and mild urinary retention. Severe meningeal signs were noted. Lumbar puncture revealed bloody cerebrospinal fluid. Magnetic resonance images revealed SSH in the ventral position spreading from levels Th1 to Th7. The patient underwent conservative treatment after which the symptoms gradually improved. Serial MRI study at 17 and 69 days after onset showed spontaneous regression of the SSH. Spinal angiography did not show any vascular malformations, but simultaneous cerebral angiography revealed a co-existing cerebral aneurysm on the C2 segment of the left internal carotid artery. It is unlikely that the cerebral aneurysm was the origin of the SSH, based on the clinical and radiographic findings. Moreover, we confirmed the unruptured nature of the aneurysm during the clipping procedure at open surgery. We report the unique case of subacute SSH occurring 8 days after childbirth without other known risk factors. The possible etiology and magnetic resonance imaging (MRI) findings in this case, and the current controversy concerning therapy for SSH are discussed.
自发性脊髓硬膜下血肿(SSH)的发生非常罕见。虽然许多神经系统疾病可在妊娠患者中因止血失衡而发展,但文献中尚无报道表明妊娠和/或分娩本身可能是急性SSH的单一危险因素。一名38岁既往健康的女性经阴道顺产分娩一名婴儿。该患者无接受抗凝剂治疗史。产后8天,她突然出现严重的肩胛间区背痛,次日双下肢出现感觉异常并伴有轻度尿潴留。发现有明显的脑膜刺激征。腰椎穿刺显示脑脊液呈血性。磁共振成像显示腹侧位置的SSH从胸1至胸7节段扩散。患者接受了保守治疗,症状逐渐改善。发病后17天和69天的系列磁共振成像研究显示SSH自发消退。脊髓血管造影未显示任何血管畸形,但同时进行的脑血管造影显示左侧颈内动脉C2段存在一个并存的脑动脉瘤。根据临床和影像学表现,脑动脉瘤不太可能是SSH的起源。此外,我们在开放手术夹闭过程中证实了动脉瘤未破裂。我们报告了这例产后8天发生的无其他已知危险因素的亚急性SSH的独特病例。讨论了该病例可能的病因、磁共振成像(MRI)表现以及目前关于SSH治疗的争议。