Kulkarni A V, Willinsky R A, Gray T, Cusimano M D
Division of Neurosurgery, St. Michael's Hospital, Toronto, Ontario, Canada.
Neurosurgery. 1998 Feb;42(2):398-400; discussion 400-1. doi: 10.1097/00006123-199802000-00125.
Spinal subdural hematoma (SSDH) is a rare entity, and cases are usually managed as surgical emergencies. We describe a patient with a SSDH who demonstrated incomplete clinical resolution with nonsurgical management, despite continued anticoagulation treatment. We provide the most complete demonstration of the magnetic resonance imaging (MRI) characteristics of a large SSDH from its initiation to its radiological resolution.
A 61-year-old woman developed a large SSDH as a complication of a lumbar puncture. Her only neurological deficit was urinary retention.
Because of the extensiveness of the hematoma and the relative neurological preservation of the patient, she was treated conservatively. Serial MRI scans were obtained at 4, 7, 13, and 25 days. The evolution of deoxyhemoglobin in the hematoma to methemoglobin was observed. By 25 days, MRI scans showed virtual resolution.
SSDHs undergo MRI signal changes that are similar to those of brain hematomas. In certain cases, even large SSDHs demonstrate swift and dramatic spontaneous resolution, despite continued anticoagulation treatment. This report suggests that there is a role for conservative management for selected cases of SSDHs.
脊髓硬膜下血肿(SSDH)是一种罕见疾病,病例通常作为外科急症处理。我们描述了一名患有SSDH的患者,尽管持续进行抗凝治疗,但非手术治疗后临床症状未完全缓解。我们提供了一个大型SSDH从形成到影像学消退的磁共振成像(MRI)特征的最完整展示。
一名61岁女性因腰椎穿刺并发症出现大型SSDH。她唯一的神经功能缺损是尿潴留。
由于血肿范围广泛且患者神经功能相对保留,对她进行了保守治疗。在第4、7、13和25天进行了系列MRI扫描。观察到血肿中脱氧血红蛋白向高铁血红蛋白的演变。到第25天,MRI扫描显示几乎完全消退。
SSDH的MRI信号变化与脑血肿相似。在某些情况下,即使是大型SSDH,尽管持续抗凝治疗,也会迅速且显著地自发消退。本报告表明,对于某些SSDH病例,保守治疗有一定作用。