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Melanotic neuroectodermal tumor of infancy: A rare case report with differential diagnosis and review of the literature

Melanotic neuroectodermal tumor of infancy is a very rare benign but locally aggressive neoplasm of neural crest origin with a high recurrence rate. It usually affects infants of less than 1 year of age. Most commonly, the lesion affects the maxilla followed by skull, mandible, brain and other extra...

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Autores principales: Bangi, Balaji Babu, Tejasvi, M. L. Avinash
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3341745/
https://www.ncbi.nlm.nih.gov/pubmed/22557910
http://dx.doi.org/10.4103/0976-237X.94559
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author Bangi, Balaji Babu
Tejasvi, M. L. Avinash
author_facet Bangi, Balaji Babu
Tejasvi, M. L. Avinash
author_sort Bangi, Balaji Babu
collection PubMed
description Melanotic neuroectodermal tumor of infancy is a very rare benign but locally aggressive neoplasm of neural crest origin with a high recurrence rate. It usually affects infants of less than 1 year of age. Most commonly, the lesion affects the maxilla followed by skull, mandible, brain and other extracranial sites. We report an 11-month-old female baby with a similar tumor involving the anterior region of maxilla along with a brief review of the literature and differential diagnosis. A wide surgical excision was performed by an intraoral approach. A 2-year follow-up of the patient showed no recurrence.
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spelling pubmed-33417452012-05-03 Melanotic neuroectodermal tumor of infancy: A rare case report with differential diagnosis and review of the literature Bangi, Balaji Babu Tejasvi, M. L. Avinash Contemp Clin Dent Case Report Melanotic neuroectodermal tumor of infancy is a very rare benign but locally aggressive neoplasm of neural crest origin with a high recurrence rate. It usually affects infants of less than 1 year of age. Most commonly, the lesion affects the maxilla followed by skull, mandible, brain and other extracranial sites. We report an 11-month-old female baby with a similar tumor involving the anterior region of maxilla along with a brief review of the literature and differential diagnosis. A wide surgical excision was performed by an intraoral approach. A 2-year follow-up of the patient showed no recurrence. Medknow Publications & Media Pvt Ltd 2012 /pmc/articles/PMC3341745/ /pubmed/22557910 http://dx.doi.org/10.4103/0976-237X.94559 Text en Copyright: © Contemporary Clinical Dentistry 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-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Bangi, Balaji Babu
Tejasvi, M. L. Avinash
Melanotic neuroectodermal tumor of infancy: A rare case report with differential diagnosis and review of the literature
title Melanotic neuroectodermal tumor of infancy: A rare case report with differential diagnosis and review of the literature
title_full Melanotic neuroectodermal tumor of infancy: A rare case report with differential diagnosis and review of the literature
title_fullStr Melanotic neuroectodermal tumor of infancy: A rare case report with differential diagnosis and review of the literature
title_full_unstemmed Melanotic neuroectodermal tumor of infancy: A rare case report with differential diagnosis and review of the literature
title_short Melanotic neuroectodermal tumor of infancy: A rare case report with differential diagnosis and review of the literature
title_sort melanotic neuroectodermal tumor of infancy: a rare case report with differential diagnosis and review of the literature
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3341745/
https://www.ncbi.nlm.nih.gov/pubmed/22557910
http://dx.doi.org/10.4103/0976-237X.94559
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