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Proboscis lateralis: a case report.

S V Yildirim1, M Unal, O Barutçu

  • 1Department of Pediatrics, Başkent University School of Medicine, Adana Hospital, Adana, Turkey.

International Journal of Pediatric Otorhinolaryngology
|October 9, 2001
PubMed
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Proboscis lateralis, a rare nasal anomaly, was observed in a 9-month-old male. The case involved left-sided heminasal aplasia and associated ocular and neurological abnormalities.

Area of Science:

  • Craniofacial anomalies
  • Pediatric rare diseases
  • Medical imaging

Background:

  • Proboscis lateralis is a rare congenital facial malformation characterized by incomplete nasal development.
  • This condition often presents with other congenital abnormalities, making diagnosis and management complex.

Observation:

  • A 9-month-old male presented with a rare left-sided proboscis lateralis.
  • The patient exhibited associated left-sided heminasal aplasia, microphthalmia, and iris and retinal coloboma.
  • Radiological examination revealed an arachnoid cyst in the temporal fossa of the brain.

Findings:

  • The case highlights a severe presentation of proboscis lateralis with concurrent ocular and intracranial anomalies.
  • Clinical and radiological findings underscore the syndromic nature of some rare facial clefts.

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Implications:

  • This case expands the understanding of proboscis lateralis spectrum and its potential associations.
  • Early and comprehensive diagnostic evaluation is crucial for patients with rare facial anomalies.
  • Multidisciplinary management is essential for addressing the complex needs of affected children.