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Congenital facial teratoma in a neonate: Surgical management and outcome

Teratomas are among the most common tumors of childhood, but craniofacial teratomas are rare. They can be diagnosed antenatally. Craniofacial teratomas may cause airway obstruction in the newborn. We present a case of a newborn male child who was diagnosed to have a facial tumor in the 8(th) month o...

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Autores principales: Kekre, Geeta, Gupta, Abhaya, Kothari, Paras, Dikshit, Vishesh, Patil, Prashant, Deshmukh, Shahji, Kulkarni, Apoorva, Deshpande, Aditi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4979331/
https://www.ncbi.nlm.nih.gov/pubmed/27563624
http://dx.doi.org/10.4103/2231-0746.186140
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author Kekre, Geeta
Gupta, Abhaya
Kothari, Paras
Dikshit, Vishesh
Patil, Prashant
Deshmukh, Shahji
Kulkarni, Apoorva
Deshpande, Aditi
author_facet Kekre, Geeta
Gupta, Abhaya
Kothari, Paras
Dikshit, Vishesh
Patil, Prashant
Deshmukh, Shahji
Kulkarni, Apoorva
Deshpande, Aditi
author_sort Kekre, Geeta
collection PubMed
description Teratomas are among the most common tumors of childhood, but craniofacial teratomas are rare. They can be diagnosed antenatally. Craniofacial teratomas may cause airway obstruction in the newborn. We present a case of a newborn male child who was diagnosed to have a facial tumor in the 8(th) month of gestation. He was delivered normally and had no respiratory or feeding difficulties. He was also found to have a cleft palate. Serum alpha fetoprotein levels were normal. He underwent excision on day of life 9. At 11 months follow-up, he is well with no evidence of recurrence and good functional outcome.
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spelling pubmed-49793312016-08-25 Congenital facial teratoma in a neonate: Surgical management and outcome Kekre, Geeta Gupta, Abhaya Kothari, Paras Dikshit, Vishesh Patil, Prashant Deshmukh, Shahji Kulkarni, Apoorva Deshpande, Aditi Ann Maxillofac Surg Case Report - Congenital Deformity Teratomas are among the most common tumors of childhood, but craniofacial teratomas are rare. They can be diagnosed antenatally. Craniofacial teratomas may cause airway obstruction in the newborn. We present a case of a newborn male child who was diagnosed to have a facial tumor in the 8(th) month of gestation. He was delivered normally and had no respiratory or feeding difficulties. He was also found to have a cleft palate. Serum alpha fetoprotein levels were normal. He underwent excision on day of life 9. At 11 months follow-up, he is well with no evidence of recurrence and good functional outcome. Medknow Publications & Media Pvt Ltd 2016 /pmc/articles/PMC4979331/ /pubmed/27563624 http://dx.doi.org/10.4103/2231-0746.186140 Text en Copyright: © Annals of Maxillofacial Surgery http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 3.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as the author is credited and the new creations are licensed under the identical terms.
spellingShingle Case Report - Congenital Deformity
Kekre, Geeta
Gupta, Abhaya
Kothari, Paras
Dikshit, Vishesh
Patil, Prashant
Deshmukh, Shahji
Kulkarni, Apoorva
Deshpande, Aditi
Congenital facial teratoma in a neonate: Surgical management and outcome
title Congenital facial teratoma in a neonate: Surgical management and outcome
title_full Congenital facial teratoma in a neonate: Surgical management and outcome
title_fullStr Congenital facial teratoma in a neonate: Surgical management and outcome
title_full_unstemmed Congenital facial teratoma in a neonate: Surgical management and outcome
title_short Congenital facial teratoma in a neonate: Surgical management and outcome
title_sort congenital facial teratoma in a neonate: surgical management and outcome
topic Case Report - Congenital Deformity
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4979331/
https://www.ncbi.nlm.nih.gov/pubmed/27563624
http://dx.doi.org/10.4103/2231-0746.186140
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