Evidence map›Paper›PMID 39020271›Full record

ArticleBMC neurology2024

Harlequin syndrome in a patient with probable hemicrania continua and exertional headache - is there a link? a case report.

Markus Miedl, Philipp Baumgartner, Leah Raffaela Disse, Konrad Peter Weber, Heiko Pohl, Susanne Wegener

Abstract readCase Reports
In one paragraph

Article in BMC neurology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Harlequin syndrome: using clinical features and autonomic testing to unmask the disorder.Clinical autonomic research : official journal of the Clinical Autonomic Research Society · 2025
    Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors.

Markus MiedlDepartment of Neurology, University Hospital Zurich, Zurich, Switzerland.
Philipp BaumgartnerDepartment of Neurology, University Hospital Zurich, Zurich, Switzerland.
Leah Raffaela DisseDepartment of Neurology, University Hospital Zurich, Zurich, Switzerland.
Konrad Peter WeberDepartment of Neurology, University Hospital Zurich, Zurich, Switzerland.
Heiko PohlDepartment of Neurology, University Hospital Zurich, Zurich, Switzerland.
Susanne WegenerDepartment of Neurology, University Hospital Zurich, Zurich, Switzerland. susanne.wegener@usz.ch.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe 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.

conclusionsThis 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.

Indexed as

Autonomic Nervous System DiseasesFlushingHypohidrosisAdultFemaleHeadacheHumansExercise (exertional) headacheHarlequin syndromeHemicrania continuaHorner’s syndromeSjögren`s syndromeSympathetic nervous systemTrigeminal autonomic headacheUnilateral flushing

Identifiers

PMID39020271
PMCPMC11253322

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.