Department of Neurology, Boston Children's Hospital, Boston, MA, USA.
Harvard Medical School, Boston, MA, USA.
Cephalalgia. 2021 Jan;41(1):122-126. doi: 10.1177/0333102420950484. Epub 2020 Aug 19.
Cerebral proliferative angiopathy is a vascular malformation associated with compromised blood-brain barrier and with migraine-like headache. Treating blood-brain barrier-compromised patients with erenumab, an anti-calcitonin gene-related peptide receptor monoclonal antibody, may be risky.
We describe a case of a 22-year-old chronic migraine patient with cerebral proliferative angiopathy who presented to our hospital in status epilepticus 2 d after his first dose of erenumab. Serial magnetic resonance imaging (MRI) studies demonstrated progressive areas of diffusion restriction including the brain tissue adjacent to the cerebral proliferative angiopathy, bilateral white matter and hippocampi. His 6-month post-presentation magnetic resonance imaging was notable for white matter injury, encephalomalacia surrounding cerebral proliferative angiopathy and bilateral hippocampal sclerosis. He remains clinically affected with residual symptoms, including refractory epilepsy and cognitive deficits.
The evidence presented in this case supports further investigation into potential deleterious side effects of erenumab in patients with compromised blood-brain barrier, such as individuals with intracranial vascular malformations.
脑增殖性血管病是一种与血脑屏障受损相关的血管畸形,伴有偏头痛样头痛。用降钙素基因相关肽受体单克隆抗体依那西普治疗血脑屏障受损的患者可能存在风险。
我们描述了一例 22 岁的慢性偏头痛合并脑增殖性血管病患者,在接受依那西普首剂量后 2 天出现癫痫持续状态。连续磁共振成像(MRI)研究显示,扩散受限区域逐渐扩大,包括脑增殖性血管病邻近的脑组织、双侧白质和海马。他发病后 6 个月的磁共振成像显示白质损伤、脑增殖性血管病周围脑软化和双侧海马硬化。他仍然受到影响,存在残留症状,包括难治性癫痫和认知障碍。
本病例提供的证据支持进一步研究依那西普在血脑屏障受损患者中的潜在有害作用,例如颅内血管畸形患者。