Department of clinical neurosciences, Neurosurgery service and Gamma knife centre, Lausanne university hospital (CHUV), Lausanne, Switzerland; Faculty of biology and medicine (FBM), university of Lausanne (UniL), Lausanne, Switzerland; Signal processing laboratory (LTS 5), École polytechnique fédérale de Lausanne (EPFL), Lausanne, Switzerland; Faculté de médecine, Sorbonne université, Paris, France; Service de neurochirurgie, Assistance publique-Hôpitaux de Paris, hôpitaux universitaires Paris-Sud, centre hospitalier universitaire de Bicêtre, Paris, France.
Service de neurochirurgie, Assistance publique-Hôpitaux de Paris, hôpitaux universitaires Paris-Sud, centre hospitalier universitaire de Bicêtre, Paris, France.
Neurochirurgie. 2020 Nov;66(5):359-364. doi: 10.1016/j.neuchi.2020.05.008. Epub 2020 Aug 28.
Subarachnoid haemorrhage (SAH), secondary to spinal hemangioblastoma (HBL), is extremely rare, with only a few case reports to date. We report the experience of our reference centre for spinal tumours and Von Hippel-Lindau (VHL) disease in patients with spinal HBL presenting with SAH. We further performed a systematic review of the literature.
We report two cases. A systematic search was performed using the PubMed, Embase and Cochrane databases, with no limit for publication date. Inclusion criteria were: patients with HBL presenting with SAH, with or without VHL. The systematic review retrieved only 10 studies, including 16 patients.
In our centre, the first case concerned radicular HBL at D12 level, presenting with spinal and brain SAH. The patient underwent uneventful microsurgical en bloc resection. Postoperative course was normal. The second case concerned HBL with SAH at the cervico-medullary junction, with rapidly fatal course. The systematic review revealed female predominance, at a median age of 40 years, with HBL predominantly located at cervical level, common preoperative symptoms being headache and signs of meningeal irritation.
In conclusion, spinal HBL is an extremely rare cause of SAH. The systematic review found putative risk factors: female gender, age 40-50 years, cervical location, and median size 2cm. Diagnosis can be difficult when presentation mimics intracerebral SAH. We advocate early surgical removal. The risk of rapidly fatal course, in case of major haemorrhage, needs to be borne in mind.
蛛网膜下腔出血(SAH)继发于脊髓血管母细胞瘤(HBL)极为罕见,迄今为止仅有少数病例报告。我们报告了我们的脊髓肿瘤参考中心和 von Hippel-Lindau(VHL)疾病患者的经验,这些患者因脊髓 HBL 引起 SAH。我们进一步对文献进行了系统回顾。
我们报告了两例病例。使用 PubMed、Embase 和 Cochrane 数据库进行了系统搜索,对出版日期没有限制。纳入标准为:HBL 患者伴有或不伴有 VHL 表现为 SAH。系统回顾仅检索到 10 项研究,包括 16 例患者。
在我们的中心,第一例病例是 D12 水平的神经根 HBL,表现为脊髓和脑 SAH。患者接受了无并发症的显微镜下整块切除术。术后恢复正常。第二例病例是颈髓交界处的 HBL 合并 SAH,病情迅速致命。系统回顾显示女性占优势,中位年龄为 40 岁,HBL 主要位于颈椎水平,常见的术前症状是头痛和脑膜刺激征。
总之,脊髓 HBL 是 SAH 的极罕见原因。系统回顾发现了一些可能的危险因素:女性、40-50 岁、颈椎位置和中位大小 2cm。当表现类似于颅内 SAH 时,诊断可能很困难。我们主张早期手术切除。在发生大出血的情况下,需要注意迅速致命的风险。