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A congenital extranasal glioma in a newborn

Nasal gliomas are extremely rare in neonates with an incidence of 1 in 20,000 to 40,000. They often are asymptomatic but can present with respiratory distress depending on the size and location of the tumor. A newborn female was prenatally diagnosed with a left nasal mass. After her birth, she was t...

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Detalles Bibliográficos
Autor principal: Bailey, Nicole A
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9772970/
https://www.ncbi.nlm.nih.gov/pubmed/36569035
http://dx.doi.org/10.1177/2050313X221144515
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author Bailey, Nicole A
author_facet Bailey, Nicole A
author_sort Bailey, Nicole A
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description Nasal gliomas are extremely rare in neonates with an incidence of 1 in 20,000 to 40,000. They often are asymptomatic but can present with respiratory distress depending on the size and location of the tumor. A newborn female was prenatally diagnosed with a left nasal mass. After her birth, she was transferred to a local children’s hospital for subspecialty evaluation and for diagnostic imaging. The mass was resected at 1 year of age. Pathology confirmed a nasal glioma. Several weeks after surgery, a nasal prosthetic device was applied to correct the nasal deformity caused by the pressure effect of the tumor. At almost 1 year of age, there was no evidence of metastasis or recurrence of the nasal glioma. The prognosis and outcome tend to be favorable. The rare case of a neonate with a congenital nasal glioma is presented.
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spelling pubmed-97729702022-12-23 A congenital extranasal glioma in a newborn Bailey, Nicole A SAGE Open Med Case Rep Case Report Nasal gliomas are extremely rare in neonates with an incidence of 1 in 20,000 to 40,000. They often are asymptomatic but can present with respiratory distress depending on the size and location of the tumor. A newborn female was prenatally diagnosed with a left nasal mass. After her birth, she was transferred to a local children’s hospital for subspecialty evaluation and for diagnostic imaging. The mass was resected at 1 year of age. Pathology confirmed a nasal glioma. Several weeks after surgery, a nasal prosthetic device was applied to correct the nasal deformity caused by the pressure effect of the tumor. At almost 1 year of age, there was no evidence of metastasis or recurrence of the nasal glioma. The prognosis and outcome tend to be favorable. The rare case of a neonate with a congenital nasal glioma is presented. SAGE Publications 2022-12-19 /pmc/articles/PMC9772970/ /pubmed/36569035 http://dx.doi.org/10.1177/2050313X221144515 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by-nc/4.0/This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (https://creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access page (https://us.sagepub.com/en-us/nam/open-access-at-sage).
spellingShingle Case Report
Bailey, Nicole A
A congenital extranasal glioma in a newborn
title A congenital extranasal glioma in a newborn
title_full A congenital extranasal glioma in a newborn
title_fullStr A congenital extranasal glioma in a newborn
title_full_unstemmed A congenital extranasal glioma in a newborn
title_short A congenital extranasal glioma in a newborn
title_sort congenital extranasal glioma in a newborn
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9772970/
https://www.ncbi.nlm.nih.gov/pubmed/36569035
http://dx.doi.org/10.1177/2050313X221144515
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