A severe cerebral infarction associated with giant cell arteritis, which developed during tocilizumab therapy and was successfully treated with intravenous cyclophosphamide.

Koji Suzuki, Mitsuhiro Akiyama, Sho Ishigaki, Yasushi Kondo, Shuntaro Saito, Jun Kikuchi, Hironari Hanaoka, Yuko Kaneko
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引用次数: 1

Abstract

Giant cell arteritis (GCA) is a large vessel vasculitis that primarily involves aorta and its major branches. Cerebral infarction is a serious complication that can occur secondary to GCA in up to 3% of patients with a mortality rate of over 50%. Due to the rarity of this severe complication, no therapeutic strategies are currently available. Furthermore, despite the recent progress in molecular-targeted therapy for GCA, it remains unknown whether tocilizumab is effective for severe ischemic complications such as cerebral infarction. The accumulation of individual cases in which this fatal complication could be treated is apparently required to build a better management of the disease. We present our case of GCA that developed severe cerebral infarction during high-dose glucocorticoid and tocilizumab therapy, and its symptoms and image findings were improved by switching to intravenous cyclophosphamide. Our case suggests that an intensive immunosuppressive therapy, including cyclophosphamide, may be necessary to stabilise this fatal complication of GCA.

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严重脑梗死伴巨细胞动脉炎,在托珠单抗治疗期间发展,静脉注射环磷酰胺成功治疗。
巨细胞动脉炎(GCA)是一种主要累及主动脉及其主要分支的大血管炎。脑梗死是一种严重的并发症,可在高达3%的患者中继发于GCA,死亡率超过50%。由于这种严重并发症的罕见性,目前尚无治疗策略。此外,尽管最近在GCA的分子靶向治疗方面取得了进展,但tocilizumab对脑梗死等严重缺血性并发症是否有效仍不清楚。显然,需要积累可以治疗这种致命并发症的病例,以建立更好的疾病管理。我们提出了我们的病例GCA,在高剂量糖皮质激素和托珠单抗治疗期间发展为严重脑梗死,其症状和图像发现通过切换到静脉注射环磷酰胺得到改善。我们的病例提示强化免疫抑制治疗,包括环磷酰胺,可能需要稳定这种致命的GCA并发症。
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