Large laryngeal vascular malformation in a 5-year-old child

Christian Sander Danstrup1, Mette Hjørringgaard Madsen2, Jesper Bille1

  • 1Ear, Nose and Throat Department, Aarhus University Hospital, Aarhus, Denmark.

BMJ Case Reports
|March 22, 2015
PubMed

Insights

A rare arteriovenous malformation (AVM) caused persistent stridor in a child, initially misdiagnosed. Prompt diagnosis and multidisciplinary care are crucial for managing complex vascular anomalies.

Area of Science:

  • Vascular Surgery
  • Pediatric Otolaryngology
  • Diagnostic Imaging

Background:

  • A 5-year-old boy presented with persistent stridor and hoarseness, initially suspected as subglottic laryngitis.
  • Standard treatments for laryngitis, including epinephrine and glucocorticoids, were ineffective, prompting further investigation.

Observation:

  • Clinical presentation included prolonged hoarseness and a deep voice, atypical for subglottic laryngitis.
  • Direct laryngoscopy and blood work did not confirm the initial diagnosis.

Findings:

  • Magnetic Resonance Imaging (MRI) and subsequent angiography revealed a bilateral arteriovenous malformation (AVM) of the lingual and superior thyroid arteries.
  • The extensive nature of this AVM necessitated referral to a specialized center for treatment.

Implications:

  • This case highlights diagnostic challenges in pediatric stridor, emphasizing the need for advanced imaging when initial assessments are inconclusive.
  • It underscores the importance of a multidisciplinary approach in diagnosing and managing rare vascular malformations.

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