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Congenital Nasal Pyriform Aperture Stenosis in Association With Polymalformative Syndrome of the Midline

Congenital nasal pyriform aperture stenosis (CNPAS) is a rare neonatal entity characterized by a reduction in the pyriform orifice of the nasal cavity. Because of its nonspecific clinical presentation as respiratory distress symptoms, it can mimic choanal atresia. Although isolated forms have been d...

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Autores principales: Tropsek, Robert, Horoi, Mihaela, Ziereisen, France
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cureus 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10498658/
https://www.ncbi.nlm.nih.gov/pubmed/37711266
http://dx.doi.org/10.7759/cureus.45153
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author Tropsek, Robert
Horoi, Mihaela
Ziereisen, France
author_facet Tropsek, Robert
Horoi, Mihaela
Ziereisen, France
author_sort Tropsek, Robert
collection PubMed
description Congenital nasal pyriform aperture stenosis (CNPAS) is a rare neonatal entity characterized by a reduction in the pyriform orifice of the nasal cavity. Because of its nonspecific clinical presentation as respiratory distress symptoms, it can mimic choanal atresia. Although isolated forms have been described, CNPAS is often associated with other congenital midline malformations. A single median incisor is usually found, with or without other cervical and maxillofacial malformations. The existence of hypothalamic-pituitary axis malformations with endocrine disorders is also possible and, in some cases, a moderate to severe intellectual deficit in association with other brain malformations. Radiological investigation is a central point in the multidisciplinary management of this type of polymalformative syndrome.
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spelling pubmed-104986582023-09-14 Congenital Nasal Pyriform Aperture Stenosis in Association With Polymalformative Syndrome of the Midline Tropsek, Robert Horoi, Mihaela Ziereisen, France Cureus Pediatrics Congenital nasal pyriform aperture stenosis (CNPAS) is a rare neonatal entity characterized by a reduction in the pyriform orifice of the nasal cavity. Because of its nonspecific clinical presentation as respiratory distress symptoms, it can mimic choanal atresia. Although isolated forms have been described, CNPAS is often associated with other congenital midline malformations. A single median incisor is usually found, with or without other cervical and maxillofacial malformations. The existence of hypothalamic-pituitary axis malformations with endocrine disorders is also possible and, in some cases, a moderate to severe intellectual deficit in association with other brain malformations. Radiological investigation is a central point in the multidisciplinary management of this type of polymalformative syndrome. Cureus 2023-09-13 /pmc/articles/PMC10498658/ /pubmed/37711266 http://dx.doi.org/10.7759/cureus.45153 Text en Copyright © 2023, Tropsek et al. https://creativecommons.org/licenses/by/3.0/This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Pediatrics
Tropsek, Robert
Horoi, Mihaela
Ziereisen, France
Congenital Nasal Pyriform Aperture Stenosis in Association With Polymalformative Syndrome of the Midline
title Congenital Nasal Pyriform Aperture Stenosis in Association With Polymalformative Syndrome of the Midline
title_full Congenital Nasal Pyriform Aperture Stenosis in Association With Polymalformative Syndrome of the Midline
title_fullStr Congenital Nasal Pyriform Aperture Stenosis in Association With Polymalformative Syndrome of the Midline
title_full_unstemmed Congenital Nasal Pyriform Aperture Stenosis in Association With Polymalformative Syndrome of the Midline
title_short Congenital Nasal Pyriform Aperture Stenosis in Association With Polymalformative Syndrome of the Midline
title_sort congenital nasal pyriform aperture stenosis in association with polymalformative syndrome of the midline
topic Pediatrics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10498658/
https://www.ncbi.nlm.nih.gov/pubmed/37711266
http://dx.doi.org/10.7759/cureus.45153
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