Schofield J R, Hassell K L
Center for Multisystem Disease, Denver, CO, USA.
Department of Medicine, 129263University of Colorado, Aurora, CO, USA.
Lupus. 2023 Mar;32(3):319-324. doi: 10.1177/09612033231153790. Epub 2023 Jan 28.
Headache, often migrainous, is common in patients with antiphospholipid antibodies, whether or not they meet Sydney criteria for a definite diagnosis of Hughes syndrome. Migraine may be a harbinger of stroke in this patient population and even refractory migraine may be highly responsive to antithrombotic therapy in this clinical context.
To summarize what is known to date about managing this important manifestation of the immune-mediated hypercoagulable Hughes syndrome.
We provide a suggested management algorithm for refractory headache in this unique patient population.
Most neurologists don't see or recognize many aPL-positive patients in their practice, so hematologists and rheumatologists who see these patients should recognize that refractory headache may be a manifestation of their immune-mediated hypercoagulable disorder and understand that the potential risks of not addressing this issue may be high.
头痛,通常为偏头痛,在抗磷脂抗体阳性患者中很常见,无论他们是否符合悉尼标准中对确诊休斯综合征的诊断。偏头痛可能是该患者群体中风的先兆,在这种临床情况下,即使是难治性偏头痛对抗血栓治疗也可能有高度反应。
总结目前已知的关于管理免疫介导的高凝性休斯综合征这一重要表现的相关内容。
我们为这一独特患者群体中的难治性头痛提供了一种建议的管理算法。
大多数神经科医生在其临床实践中很少见到或认识许多抗磷脂抗体阳性患者,因此诊治这些患者的血液科医生和风湿科医生应认识到难治性头痛可能是其免疫介导的高凝性疾病的一种表现,并明白不解决这个问题可能存在的潜在风险很高。