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Research and review articles are invited for publication in September - October 2026 (Volume 18, Issue 1) Submit manuscript

Laughter-Induced Syncope: A rare subtype of situational reflex syncope: A case report

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  • Laughter-Induced Syncope: A rare subtype of situational reflex syncope: A case report

Erhad Bilaro 1, *, George Kwesiga 2 and Bikolimana Masoud 2

1 Department of Internal Medicine, Kibaha College of Health and Allied Sciences, Tanzania.
2 Department of Outpatient, Dr. Ole Lengine’s Memorial Hospital, Dar es salaam, Tanzania.
 
Case Study
Magna Scientia Advanced Research and Reviews, 2025, 15(01), 098-101
Article DOI: 10.30574/msarr.2025.15.1.0114
DOI url: https://doi.org/10.30574/msarr.2025.15.1.0114
Received on 19 August 2025; revised on 25 September 2025; accepted on 27 September 2025
Background: Syncope is a common clinical presentation at medical facilities, often challenging to diagnose due to its diverse etiologies. Laughter-induced syncope (LIS) is a rare, under-recognized variant of syncope, triggered by intense laughter. While generally benign, it may be misdiagnosed as seizure or cardiac syncope without careful history-taking.
Case Presentation: A 35-year-old woman presented with recurrent brief episodes of loss of consciousness exclusively precipitated by sustained laughter.  Each episode lasted approximately 30 seconds with no tonic-clonic movements, incontinence, or postictal confusion. Episodes were self-limited with spontaneous, complete recovery. Past medical history and family history were all unremarkable. Physical examination, laboratory investigations, electrocardiography, echocardiography, and electroencephalography were all normal. Alternative causes, including cardiac arrhythmias, structural heart disease, seizures, metabolic disturbances, and cataplexy, were excluded.
Discussion: LIS likely results from a combination of increased intrathoracic pressure during vigorous laughter, transient reduction in venous return, reflex-mediated bradycardia or vasodilation, and subsequent cerebral hypoperfusion. Diagnosis is clinical, relying on detailed patient history and witness accounts, with exclusion of alternative causes. Management is primarily conservative, focusing on patient education, avoidance of prolonged intense laughter, and reassurance regarding the benign nature of the condition and its prognosis.
Conclusion: This report highlights the importance of systematic evaluation and careful history-taking in assessing transient loss of consciousness. Recognition of LIS prevents unnecessary investigations, facilitates accurate and timely diagnosis and provides reassurance to patients and their families on the benign nature of the condition. It also raises awareness among clinicians particularly in differentiating reflex syncope from potentially serious causes of transient loss of consciousness.
Laughter-Induced Syncope; Situational Syncope; Reflex Syncope; Transient Loss of Consciousness
https://msarr.magnascientiapub.com/sites/default/files/fulltext_pdf/MSARR-2025-…

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Erhad Bilaro, George Kwesiga and Bikolimana Masoud. Laughter-Induced Syncope: A rare subtype of situational reflex syncope: A case report. Magna Scientia Advanced Research and Reviews, 2025, 15(1), 098-101. Article DOI: https://doi.org/10.30574/msarr.2025.15.1.0114

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