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A Rare Case of Nasal Glial Heterotopia in an Infant

Glial heterotopias are the displacement of neuroglial tissue in extracranial sites. Nasal glial heterotopias can be of three types-extranasal, intranasal and mixed. Root of the nose is the most common location. These are rare anomalies with an incidence of 1 case in 20,000–40,000 live births. Here w...

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Autores principales: Tahlan, Karishma, Tanveer, Nadeem, Kumar, Harresh, Diwan, Himanshi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer - Medknow 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7646421/
https://www.ncbi.nlm.nih.gov/pubmed/33209002
http://dx.doi.org/10.4103/JCAS.JCAS_148_19
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author Tahlan, Karishma
Tanveer, Nadeem
Kumar, Harresh
Diwan, Himanshi
author_facet Tahlan, Karishma
Tanveer, Nadeem
Kumar, Harresh
Diwan, Himanshi
author_sort Tahlan, Karishma
collection PubMed
description Glial heterotopias are the displacement of neuroglial tissue in extracranial sites. Nasal glial heterotopias can be of three types-extranasal, intranasal and mixed. Root of the nose is the most common location. These are rare anomalies with an incidence of 1 case in 20,000–40,000 live births. Here we report the case of a 6-month-old infant with a congenital mass located at the root of the nose. Non-contrast computed tomography studies showed no evidence of intracranial communication of the lesion. The mass was excised, and on histopathological examination, it showed glial tissue with astrocytes in a fibrillary background and fibroconnective tissue. Masson’s trichrome stain showed the red staining of the glial tissue, whereas the background fibrosis was stained blue. On immunohistochemistry, glial fibrillary acidic protein was positive. Hence, the diagnosis of nasal glial heterotropia was made. The patient had an uneventful postoperative period.
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spelling pubmed-76464212020-11-17 A Rare Case of Nasal Glial Heterotopia in an Infant Tahlan, Karishma Tanveer, Nadeem Kumar, Harresh Diwan, Himanshi J Cutan Aesthet Surg Case Report Glial heterotopias are the displacement of neuroglial tissue in extracranial sites. Nasal glial heterotopias can be of three types-extranasal, intranasal and mixed. Root of the nose is the most common location. These are rare anomalies with an incidence of 1 case in 20,000–40,000 live births. Here we report the case of a 6-month-old infant with a congenital mass located at the root of the nose. Non-contrast computed tomography studies showed no evidence of intracranial communication of the lesion. The mass was excised, and on histopathological examination, it showed glial tissue with astrocytes in a fibrillary background and fibroconnective tissue. Masson’s trichrome stain showed the red staining of the glial tissue, whereas the background fibrosis was stained blue. On immunohistochemistry, glial fibrillary acidic protein was positive. Hence, the diagnosis of nasal glial heterotropia was made. The patient had an uneventful postoperative period. Wolters Kluwer - Medknow 2020 /pmc/articles/PMC7646421/ /pubmed/33209002 http://dx.doi.org/10.4103/JCAS.JCAS_148_19 Text en Copyright: © 2020 Journal of Cutaneous and Aesthetic Surgery http://creativecommons.org/licenses/by-nc-sa/4.0 This is an open access journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms.
spellingShingle Case Report
Tahlan, Karishma
Tanveer, Nadeem
Kumar, Harresh
Diwan, Himanshi
A Rare Case of Nasal Glial Heterotopia in an Infant
title A Rare Case of Nasal Glial Heterotopia in an Infant
title_full A Rare Case of Nasal Glial Heterotopia in an Infant
title_fullStr A Rare Case of Nasal Glial Heterotopia in an Infant
title_full_unstemmed A Rare Case of Nasal Glial Heterotopia in an Infant
title_short A Rare Case of Nasal Glial Heterotopia in an Infant
title_sort rare case of nasal glial heterotopia in an infant
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7646421/
https://www.ncbi.nlm.nih.gov/pubmed/33209002
http://dx.doi.org/10.4103/JCAS.JCAS_148_19
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