抗降钙素基因相关肽单克隆抗体对结膜注射和撕裂反应的难治性单侧神经痛性头痛发作1例报告。

Gabriel Bsteh, Christian Bsteh, Gregor Broessner
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引用次数: 3

摘要

背景:短时间单侧神经性头痛发作伴结膜注射撕裂(SUNCT)是一种罕见但严重致残的三叉神经自主神经性头痛,缺乏循证治疗。病例:我们报告了一例67岁的慢性SUNCT患者,对各种符合指南的治疗尝试都难治,对galcanezumab反应良好。结论:本病例报告表明,针对降钙素基因相关肽的单克隆抗体,特别是galcanezumab,可能是SUNCT的一种治疗选择,值得进一步研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Refractory short-lasting unilateral neuralgiform headache attacks with conjunctival injection and tearing responsive to anti-calcitonin gene-related peptide monoclonal antibodies: A case report.

Background: Short-lasting unilateral neuralgiform headache attacks with conjunctival injection and tearing (SUNCT) is a rare but severely disabling variant within the spectrum of trigeminal autonomic cephalalgia lacking evidence-based treatment.

Case: We report a case of chronic SUNCT in a 67-year-old man refractory to various guideline-conforming treatment attempts responding excellently to galcanezumab.

Conclusions: This case report indicates that monoclonal antibodies against calcitonin gene-related peptide, specifically galcanezumab, might be a treatment option for SUNCT warranting further investigation.

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