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Journals / The Journal of Pediatric Research / 2018 / Cilt: 5 - Sayı: 1

Nasal heterotopy in a Newborn Infant: A Case Report

Tuğba KAYA BARSAN
Ayşe Aydan KÖSE
AYŞE NESLİHAN TEKİN
Pages
54–56
DOI
—
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AI Summary & Key Takeaways

AI Insight
⚡ TL;DR(Too Long; Didn't Read)

Although rare, because of their potential to connect to the central nervous system, these disorders are clinically important.

📌 3 Key Takeaways

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Objective & Hypothesis:Glial heterotopias are rare, congenital, benign, midline, non-teratomatous extracranial glial tissues which are mostly present in the nose and may masquerade as encephalocele or dermoid cyst.
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Key Findings & Data:These masses appear to share a similar embryogenic origin.
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Conclusion & Impact:Although rare, because of their potential to connect to the central nervous system, these disorders are clinically important.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Domain Parameters

Abstract

Glial heterotopias are rare, congenital, benign, midline, non-teratomatous extracranial glial tissues which are mostly present in the nose and may masquerade as encephalocele or dermoid cyst. These masses appear to share a similar embryogenic origin. Herein, we present a neonatal nasal glioma on the nasal root and glabella area. Although rare, because of their potential to connect to the central nervous system, these disorders are clinically important.

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Cite This Article

BARSAN, T. K., KÖSE, A. A., TEKİN, A. N. (2018). Nasal heterotopy in a Newborn Infant: A Case Report. The Journal of Pediatric Research, Cilt: 5 - Sayı: 1, 54–56. https://ajindex.com/articles/362773

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