Evidence map›Paper›PMID 41709878›Full record

ArticleCase reports in neurology

Tapia's Syndrome following Noninvasive Continuous Positive Airway Pressure Therapy: A Case Report.

Otabek Pulatov, Diego Rafael Alvarez Vega, Fatima Syed, Matthew Bokhari

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Article in Case reports in neurology. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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0 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Otabek PulatovNew York University Grossman Long Island School of Medicine, Mineola, NY, USA.
Diego Rafael Alvarez VegaNew York University Grossman Long Island School of Medicine, Mineola, NY, USA.
Fatima SyedDepartment of Neurology, NYU Langone Health - Long Island, Mineola, NY, USA.
Matthew BokhariDepartment of Neurology, NYU Langone Health - Long Island, Mineola, NY, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Tapia's syndrome is a rare neurological condition defined by concurrent unilateral paralysis of the vagus (cranial nerve X) and hypoglossal (cranial nerve XII) nerves. It is most commonly reported as an iatrogenic complication of procedures involving airway manipulation, such as orotracheal intubation. This report describes a unique case of Tapia's syndrome with a temporal association to the initiation of noninvasive continuous positive airway pressure (CPAP) therapy. Case Presentation: A 66-year-old female presented with a four-day history of acute-onset dysphonia, dysphagia, and right-sided tongue deviation. Her symptoms began shortly after initiating CPAP therapy with a full-face mask for newly diagnosed obstructive sleep apnea. She had also recently received multiple vaccinations. Clinical examination revealed right-sided vagus and hypoglossal nerve palsies, and laryngoscopy confirmed right vocal cord paralysis. Extensive diagnostic evaluation, including magnetic resonance imaging and angiography of the brain and neck, effectively excluded central nervous system pathologies such as stroke, demyelinating disease, or mass lesions and diagnosis of Tapia's syndrome was made. The patient was managed by discontinuing CPAP and administering a course of oral corticosteroids, alongside speech and swallowing therapy. She experienced a near-complete resolution of her symptoms over 6 weeks. Conclusion: This case suggests that Tapia's syndrome can be a rare complication of noninvasive airway support. A multifactorial etiology involving mechanical nerve compression from the CPAP apparatus, potentially compounded by an immune-mediated nerve sensitization from recent vaccinations, should be considered in the differential diagnosis of lower cranial neuropathies.

Indexed as

Case reportContinuous positive airway pressureCranial nerve palsyTapia’s syndrome

Identifiers

PMID41709878
PMCPMC12912766

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