病例报告:一名可能患有持续性头痛和劳累性头痛的患者的哈勒金综合征--两者之间有联系吗?

IF 2.2 3区 医学 Q3 CLINICAL NEUROLOGY BMC Neurology Pub Date : 2024-07-17 DOI:10.1186/s12883-024-03731-y
Markus Miedl, Philipp Baumgartner, Leah Raffaela Disse, Konrad Peter Weber, Heiko Pohl, Susanne Wegener
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引用次数: 0

摘要

背景:哈奎因综合征是一种罕见的自主神经系统疾病,其特征是在暴露于高温或体力活动后单侧脸部潮红和出汗减少。它由交感神经功能障碍引起,最常见的是特发性。初次出现时必须排除潜在病理(如颈动脉剥离、肿瘤)引起的继发性发展。有证据表明,头颅自律神经系统参与了三叉神经自律神经性头痛(如持续性头痛)的病理生理学。因此,哈雷综合征和三叉神经自律性头痛疾病的病理生理学重叠似乎是可信的。然而,从未有报道称哈雷金综合征与连续性头痛伴发:本文描述的是一名 42 岁女性患者在我院头痛科就诊的病例。患者报告了持续性单侧头痛,右侧为拖曳性或挤压性,伴有三叉神经自主神经症状,包括流泪、鼻塞、结膜注射和霍纳综合征,对 75 毫克/天的吲哚美辛治疗有反应。初诊五个月后,患者注意到慢跑后右上脸部苍白。经诊断,她患上了哈勒普综合征。此外,她在剧烈运动时出现持续时间短的双侧搏动性头痛,与劳累性头痛一致。综合诊断评估包括头颅和颈椎磁共振成像扫描、实验室检查和活组织检查,最终确诊为斯约格伦综合征。这一发现表明,三叉神经-自主神经功能障碍可能是特发性的,也可能是斯约格伦综合征的直接表现:本报告记录了一例罕见的头痛合并症,类似于可能的连续性头痛和哈勒金综合征(甚至是劳累性头痛)。它从临床角度说明了自律神经系统的基本解剖结构,并强调了交感神经活动异常与三叉神经自律神经性头痛之间存在病理生理联系的假设。
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Harlequin syndrome in a patient with probable hemicrania continua and exertional headache - is there a link? a case report.

Background: The harlequin syndrome is a rare disorder of the autonomic nervous system characterized by unilateral diminished flushing and sweating of the face following exposure to heat or physical activity. It results from sympathetic dysfunction and most commonly occurs idiopathically. A secondary development due to an underlying pathology (e.g., carotid artery dissection, tumors) must be excluded at first appearance. There is evidence that the cranial autonomic system is involved in the pathophysiology of trigeminal autonomic headaches like hemicrania continua. Therefore, an overlap in the pathophysiology of harlequin syndrome and trigeminal autonomic headache disorders seems plausible. However, the association of a harlequin syndrome with hemicrania continua was never reported.

Case presentation: This work describes the case of a 42-year-old female patient presenting to our headache unit. The patient reported persisting unilateral headache of the right side of dragging or squeezing character accompanied by trigeminal autonomic symptoms, including lacrimation, nasal congestion, conjunctival injection and Horner's syndrome, and was responsive to treatment with 75mg/d indomethacin. Five months after the initial consultation, the patient noted that the upper right quadrant of her face was pale after jogging. A harlequin syndrome was diagnosed. Further, she developed a short-lasting, bilateral headache of pulsatile character during strenuous exercise consistent with exertional headache. Comprehensive diagnostic evaluations, encompassing cranial and cervical MRI scans, laboratory tests, and biopsies, culminated in the diagnosis of Sjögren's syndrome. This finding suggests that the trigemino-autonomic dysfunction may either be idiopathic or a direct manifestation of Sjögren's syndrome.

Conclusions: This report documents the case of a rare combination of a headache resembling probable hemicrania continua and the harlequin syndrome (and even exertional headache). It illustrates the underlying anatomy of the autonomic nervous system in a clinical context and emphasizes the hypothesis of a pathophysiological link between abnormal sympathetic activity and trigeminal autonomic headaches.

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来源期刊
BMC Neurology
BMC Neurology 医学-临床神经学
CiteScore
4.20
自引率
0.00%
发文量
428
审稿时长
3-8 weeks
期刊介绍: BMC Neurology is an open access, peer-reviewed journal that considers articles on all aspects of the prevention, diagnosis and management of neurological disorders, as well as related molecular genetics, pathophysiology, and epidemiology.
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