作为抗磷脂综合征罕见并发症的脑脊液鼻出血的处理方法

Elissa Xian, Joel Hardman, Geoffrey Parker, Arjuna Nirmalananda
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引用次数: 0

摘要

抗磷脂综合征是一种复杂的自身免疫性疾病,可在全身任何血管床反复形成血栓。颈静脉血栓形成非常罕见,发生率仅为 0.9%,通常不会因颅内压升高而导致脑脊液鼻出血。一名 54 岁的患者因脑脊液(CSF)鼻出血和头痛就诊 9 个月,其背景是抗磷脂综合征。检查结果显示上腔静脉(SVC)和右颈内静脉(IJV)阻塞,颅内静脉压中度升高。她的脑磁共振成像(MRI)与脑脊液漏一致。患者成功接受了阻塞的SVC和右侧IJV血管内支架置入术,随后又接受了左侧乙状气室后部脑膜疝的手术修复。对于这种具有挑战性的病例,建议结合使用血管内技术和手术修复。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Management of cerebrospinal fluid rhinorrhea as a rare complication of antiphospholipid syndrome
Antiphospholipid syndrome is a complex autoimmune condition associated with the formation of recurrent thrombosis in any vascular bed throughout the body. Jugular vein thrombosis is very rare with only a 0.9% occurrence and is not typically associated with cerebrospinal rhinorrhea as a result of raised intracranial pressure. A 54-year-old patient presented with a 9-month history of cerebrospinal fluid (CSF) rhinorrhea and headache on a background of antiphospholipid syndrome. Investigations showed a superior vena cava (SVC) and right internal jugular vein (IJV) obstruction with moderately elevated intracranial venous pressures. Her magnetic resonance imaging (MRI) brain was consistent with a CSF leak. The patient underwent successful endovascular stenting of her obstructed SVC and right IJV followed by surgical repair of a herniating meningocele in the posterior left ethmoid air cells. CSF rhinorrhea is uncommon and never previously reported associated with SVC thrombosis induced by antiphospholipid syndrome. A combination of endovascular techniques and surgical repair is recommended for this challenging presentation.
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