Episodic cluster headache with suspected giant cell arteritis, sinusitis-related headache, and dietary triggers: a case report.

IF 2.5 Q2 CLINICAL NEUROLOGY
Frontiers in pain research (Lausanne, Switzerland) Pub Date : 2026-07-23 eCollection Date: 2026-01-01 DOI:10.3389/fpain.2026.1884385
Shusheng Jiao, Ning Zhen
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引用次数: 0

Abstract

Background: Cluster headache is a primary trigeminal autonomic cephalalgia characterized by severe, strictly unilateral orbital/periorbital pain with ipsilateral autonomic features. It is rare for a patient with cluster headache to have coexisting multiple headache disorders and experience unusual triggers.

Case presentation: A 53-year-old male with a 14-year history of episodic cluster headache presented with his third cluster episode. He exhibited strictly unilateral left orbital/periorbital/temporal drilling pain [Visual Analogue Scale (VAS) 9-10/10], ipsilateral conjunctival injection, lacrimation, rhinorrhea, and agitation. Notably, during the second episode (2015), left maxillary sinusitis was identified and surgically treated, leading to immediate and complete headache resolution. During the current episode, physical examination revealed left temporal artery nodularity and tenderness-raising suspicion of giant cell arteritis. However, the erythrocyte sedimentation rate and C-reactive protein levels were within the normal range. Brain MRI/MRA revealed only nonspecific white matter changes, along with suspected wall thickening of the left superficial temporal artery. The patient declined temporal artery ultrasound, high-resolution MRI, and biopsy. In accordance with clinical guidelines, the patient was administered comprehensive treatment for cluster headache. Given the suspicion of giant cell arteritis, empirical prednisone was also initiated at a dose of 1 mg/kg/day. By day 3 of treatment, attack frequency had reduced from daily to 3-4 times per week, pain intensity decreased from VAS 10/10 to 3-6/10, attacks resolved within 30 min either spontaneously or after zolmitriptan, and temporal artery nodules had markedly diminished. Interestingly, during follow-up, the patient reported that ingestion of soy sauce or vinegar consistently triggered an unusual throat discomfort followed by headache within 30 min, whereas avoidance of these substances resulted in no attacks. The patient's strict avoidance of soy sauce and vinegar led to a marked reduction in headache frequency over a short period, ultimately resulting in a complete absence of headache episodes. He remains under follow-up.

Conclusion: This case highlights an unusual concurrence of episodic cluster headache with suspected giant cell arteritis and possible sinusitis-related headache in a single patient. The potential role of soy sauce and vinegar as triggers for cluster headache warrants further validation with extended follow-up and a larger case series.

阵发性丛集性头痛伴怀疑巨细胞动脉炎、鼻窦炎相关头痛及饮食诱因1例报告。
背景:丛集性头痛是一种原发性三叉神经自主神经性头痛,其特征是伴同侧自主神经特征的严重单侧眶/眶周疼痛。这是罕见的患者丛集性头痛有共存的多种头痛疾病和经历不寻常的触发。病例介绍:53岁男性,14年阵发性丛集性头痛病史,第三次出现丛集性头痛。他表现出严格的单侧左眼眶/眶周/颞部钻孔痛[视觉模拟评分(VAS) 9-10/10],同侧结膜注射,流泪,鼻漏和躁动。值得注意的是,在第二次发作(2015年)期间,发现了左上颌窦炎并进行了手术治疗,导致头痛立即完全解决。在这次发作中,体格检查显示左颞动脉结节和压痛,怀疑巨细胞动脉炎。但红细胞沉降率和c反应蛋白水平在正常范围内。脑MRI/MRA仅显示非特异性白质改变,同时疑似左侧颞浅动脉壁增厚。患者颞动脉超声、高分辨率MRI和活检下降。根据临床指南,对患者进行集束性头痛的综合治疗。考虑到怀疑巨细胞动脉炎,经验性泼尼松也以1mg /kg/天的剂量开始。到治疗的第3天,发作频率从每天减少到每周3-4次,疼痛强度从VAS 10/10下降到3-6/10,发作在30分钟内自行或服用唑米曲坦后消退,颞动脉结节明显减少。有趣的是,在随访期间,患者报告说,摄入酱油或醋持续引发不寻常的喉咙不适,随后在30分钟内头痛,而避免这些物质导致没有发作。患者严格避免酱油和醋导致头痛频率在短时间内显著减少,最终导致头痛发作完全消失。他仍在接受随访。结论:本病例突出了一个罕见的阵发性丛集性头痛同时伴有疑似巨细胞动脉炎和可能的鼻窦炎相关头痛的病例。酱油和醋作为丛集性头痛触发因素的潜在作用值得通过延长随访和更大的病例系列进一步验证。
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来源期刊
CiteScore
2.10
自引率
0.00%
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审稿时长
13 weeks
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