Evidence map›Paper›PMID 42253675›Full record

ArticleInternational journal of surgery case reports2026

Tapia syndrome after orthognathic surgery: a case report.

Reza Sharifi, Mohammad Nomani, Rahele Mousavi

Abstract readCase Reports
In one paragraph

Article in International journal of surgery case reports, 2026. 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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0citing papers in PubMed
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1 · What the graph read from it

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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

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3 · Its place in the literature

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0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

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5 · Who and what money

Authors and funding

3 authors.

Reza SharifiDepartment of Oral and Maxillofacial Surgery, Cranio Maxillofacial Research Center, Shariati Hospital, Tehran University of Medical Sciences, Tehran, Iran.
Mohammad NomaniDepartment of Oral and Maxillofacial Surgery, Dental School, Tehran University of Medical Sciences, Tehran, Iran.
Rahele MousaviDepartment of Oral and Maxillofacial Surgery, Dental School, Tehran University of Medical Sciences, Tehran, Iran.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction and importance: Tapia syndrome is a cranial neuropathy. It involves the hypoglossal and recurrent laryngeal nerves. The syndrome may follow airway manipulation or prolonged intubation. We report a case of Tapia syndrome, its presentation, management, and outcome. Presentation: A 45-year-old man with skeletal Class III malocclusion underwent orthognathic surgery. Nasotracheal intubation was difficult and required repeated maneuvers and a second attempt. During extubation, the patient developed laryngospasm and hoarseness, which necessitated re-intubation and 24 hours of mechanical ventilation. After successful re-extubation, he manifested complete tongue immobility and dysarthria. Electromyography performed on postoperative day 10 demonstrated partial right and complete left hypoglossal nerve paralysis. These findings are consistent with Tapia syndrome and correlate with clinical leftward tongue deviation. Discussion: Management included corticosteroid therapy and initiation of speech and language therapy. We added an adjunctive local low-level laser therapy. Serial clinical photographs and examinations documented steady improvement within 3 months. Conclusion: Early electrodiagnostic confirmation and multidisciplinary care were associated with near-complete functional recovery by 3 months. The report underscores the importance of careful airway techniques, vigilance for early postoperative bulbar signs, and early rehabilitation to optimize outcomes in iatrogenic cranial nerve injury.

Indexed as

case reportcorticosteroid therapycranial nerve XII palsyhypoglossal nerve paralysishypoglossal nerve paralysis/palsylaryngospasmorthognathic surgeryTapia syndrome

Identifiers

PMID42253675
PMCPMC13236253

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