Department of Neurosurgery, Klinikum Rechts der Isar, Technical University Munich, Munich, Germany.
Department of Neuroradiology, Klinikum Rechts der Isar, Technical University Munich, Munich, Germany.
Acta Neurochir (Wien). 2024 Aug 28;166(1):353. doi: 10.1007/s00701-024-06240-6.
Spontaneous spinal hematoma (SSH), a rare neurological disorder, demands immediate diagnostic evaluation and intervention to prevent lasting deficits. This case series analyzes instances, particularly highlighting cases where vascular causes were identified despite inconclusive initial imaging.
In a retrospective study of 20 patients treated for SSH at a Level I spine center from 01/01/2017 to 11/15/2023, we examined demographics, clinical presentation, imaging, and treatment details. Excluding traumatic cases, we present 4 instances of SSH associated with diverse vascular pathologies.
Patient ages ranged from 39 to 85 years, with a median age of 66 years. 45% were male, and 55% were female. Among 20 cases, 14 were epidural hematomas, 4 subdural, 1 combined epidural and subdural, and 1 subarachnoid hemorrhage. 85% presented with neurological deficits, while 3 solely had pain-related symptoms. 55% were under anticoagulant medication, and vascular anomalies were found in 25% of cases. The cause of SSH remained unclear in 20% of cases. MRI was performed for all patients, and DSA was conducted in 25% of cases. The 4 highlighted cases involved individuals with distinct vascular pathologies managed surgically.
Urgent attention is crucial for SSH due to possible lasting neurological consequences. The study emphasizes comprehensive diagnostics and surgical exploration, especially in cases with unclear etiology, to identify and address vascular causes, preventing hematoma progression or recurrence. Despite their rarity, vascular malformations contributing to spinal hematomas warrant particular attention.
自发性脊柱血肿(SSH)是一种罕见的神经系统疾病,需要立即进行诊断评估和干预,以防止出现持久的损伤。本病例系列分析了一些病例,特别是强调了在初始影像学检查结果不明确的情况下发现血管原因的情况。
在对 2017 年 1 月 1 日至 2023 年 11 月 15 日在一级脊柱中心接受 SSH 治疗的 20 名患者进行回顾性研究中,我们检查了人口统计学、临床表现、影像学和治疗细节。排除外伤性病例后,我们报告了 4 例与不同血管病变相关的 SSH 病例。
患者年龄为 39 至 85 岁,中位数年龄为 66 岁。45%为男性,55%为女性。20 例中,14 例为硬膜外血肿,4 例为硬膜下血肿,1 例为硬膜外和硬膜下混合血肿,1 例为蛛网膜下腔出血。85%的患者出现神经功能缺损,而 3 例仅表现为与疼痛相关的症状。55%的患者正在接受抗凝药物治疗,25%的患者发现血管异常。20%的病例 SSH 的病因仍不清楚。所有患者均行 MRI 检查,25%的患者行 DSA 检查。4 例重点病例涉及到 4 名具有不同血管病变的患者,这些患者接受了手术治疗。
由于可能导致持久的神经后果,SSH 需要立即关注。该研究强调了全面的诊断和手术探索,特别是在病因不明的情况下,以识别和处理血管原因,防止血肿进展或复发。尽管血管畸形导致脊柱血肿的情况很少见,但需要特别注意。