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[Supernumerary nostril].

G Cuervo de la Calle1, E Viviente Rodríguez, A Capitán Guarnizo

  • 1Servicio de ORL, Hospital General Universitario, Murcia.

Acta Otorrinolaringologica Espanola
|June 16, 2004
PubMed
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Supernumerary nostril, a rare congenital anomaly, often requires surgical correction. This case highlights a triple nostril linked with auricular hypoplasia, emphasizing the need for surgical intervention in such rare conditions.

Area of Science:

  • Otolaryngology
  • Developmental Biology
  • Pediatric Surgery

Background:

  • Supernumerary nostril is an extremely rare congenital anomaly stemming from aberrant embryological development.
  • This condition can manifest as a narrow cavity, either opening into the adjacent nasal cavity or terminating blindly.
  • It may occur in isolation or be associated with other congenital anomalies.

Observation:

  • A rare case of a triple nostril is presented.
  • The triple nostril anomaly was observed in association with congenital auricular hypoplasia.
  • This presentation underscores the varied clinical manifestations of supernumerary nostrils.

Findings:

  • The presented case involves a triple nostril, a rare congenital anomaly.
  • The anomaly was associated with congenital auricular hypoplasia, indicating potential syndromic presentation.

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  • Surgical treatment is the definitive management for supernumerary nostrils.
  • Implications:

    • This case contributes to the limited literature on supernumerary nostrils, particularly when associated with other anomalies.
    • Understanding the embryological basis is crucial for diagnosing and managing these rare conditions.
    • Surgical correction is essential for functional and aesthetic outcomes in patients with supernumerary nostrils.