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Diagnosis and Surgical Management of Congenital Intranasal Teratoma in a Newborn: A Rare Case Report

Teratomas are the most common germ cell tumors of childhood. Head and neck teratomas, however, account for less than five percent of all teratomas. Considered rare at an incidence of 1 in 20,000 to 40,000 live births, they may occur in the cervical region, nasopharynx, brain, orbit, or oropharynx. T...

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Autores principales: Yeo, W. X., Tan, K. K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5933031/
https://www.ncbi.nlm.nih.gov/pubmed/29850332
http://dx.doi.org/10.1155/2018/1403912
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author Yeo, W. X.
Tan, K. K.
author_facet Yeo, W. X.
Tan, K. K.
author_sort Yeo, W. X.
collection PubMed
description Teratomas are the most common germ cell tumors of childhood. Head and neck teratomas, however, account for less than five percent of all teratomas. Considered rare at an incidence of 1 in 20,000 to 40,000 live births, they may occur in the cervical region, nasopharynx, brain, orbit, or oropharynx. Teratoma presenting as an isolated intranasal mass is extremely rare. In this report, we describe a case of a mature teratoma arising from the roof of the nasal cavity presenting as an isolated intranasal mass, the first of its kind from our literature review. The tumor was resected endoscopically with no recurrence detected.
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spelling pubmed-59330312018-05-30 Diagnosis and Surgical Management of Congenital Intranasal Teratoma in a Newborn: A Rare Case Report Yeo, W. X. Tan, K. K. Case Rep Otolaryngol Case Report Teratomas are the most common germ cell tumors of childhood. Head and neck teratomas, however, account for less than five percent of all teratomas. Considered rare at an incidence of 1 in 20,000 to 40,000 live births, they may occur in the cervical region, nasopharynx, brain, orbit, or oropharynx. Teratoma presenting as an isolated intranasal mass is extremely rare. In this report, we describe a case of a mature teratoma arising from the roof of the nasal cavity presenting as an isolated intranasal mass, the first of its kind from our literature review. The tumor was resected endoscopically with no recurrence detected. Hindawi 2018-04-19 /pmc/articles/PMC5933031/ /pubmed/29850332 http://dx.doi.org/10.1155/2018/1403912 Text en Copyright © 2018 W. X. Yeo and K. K. Tan. http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Yeo, W. X.
Tan, K. K.
Diagnosis and Surgical Management of Congenital Intranasal Teratoma in a Newborn: A Rare Case Report
title Diagnosis and Surgical Management of Congenital Intranasal Teratoma in a Newborn: A Rare Case Report
title_full Diagnosis and Surgical Management of Congenital Intranasal Teratoma in a Newborn: A Rare Case Report
title_fullStr Diagnosis and Surgical Management of Congenital Intranasal Teratoma in a Newborn: A Rare Case Report
title_full_unstemmed Diagnosis and Surgical Management of Congenital Intranasal Teratoma in a Newborn: A Rare Case Report
title_short Diagnosis and Surgical Management of Congenital Intranasal Teratoma in a Newborn: A Rare Case Report
title_sort diagnosis and surgical management of congenital intranasal teratoma in a newborn: a rare case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5933031/
https://www.ncbi.nlm.nih.gov/pubmed/29850332
http://dx.doi.org/10.1155/2018/1403912
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