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Intradural Eosinophilic Granuloma Invading Skull: Case Report and Review of the Literature

Eosinophilic granuloma is a localized form of Langerhans cell histiocytosis, most commonly involving the skeletal system. Their origin from the dura is rare with only a handful of cases on record. We present one such rare case of an eosinophilic granuloma originating from the dura mater with seconda...

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Autores principales: Mardi, Kavita, Thakur, R. C., Negi, Lalita
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5652098/
https://www.ncbi.nlm.nih.gov/pubmed/29114286
http://dx.doi.org/10.4103/ajns.AJNS_47_15
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author Mardi, Kavita
Thakur, R. C.
Negi, Lalita
author_facet Mardi, Kavita
Thakur, R. C.
Negi, Lalita
author_sort Mardi, Kavita
collection PubMed
description Eosinophilic granuloma is a localized form of Langerhans cell histiocytosis, most commonly involving the skeletal system. Their origin from the dura is rare with only a handful of cases on record. We present one such rare case of an eosinophilic granuloma originating from the dura mater with secondary osseous invasion in an 11-year-old female child who presented with a swelling in the right parietal region. Magnetic resonance imaging demonstrated an enhancing mass with a wide dural attachment with a lytic lesion in the overlying skull. Right parietal extended craniotomy was done with the excision of mass from the dura. Histopathological features of mass were characteristic of eosinophilic granuloma which was confirmed by positive immunohistochemical staining for CD1a.
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spelling pubmed-56520982017-11-07 Intradural Eosinophilic Granuloma Invading Skull: Case Report and Review of the Literature Mardi, Kavita Thakur, R. C. Negi, Lalita Asian J Neurosurg Case Report Eosinophilic granuloma is a localized form of Langerhans cell histiocytosis, most commonly involving the skeletal system. Their origin from the dura is rare with only a handful of cases on record. We present one such rare case of an eosinophilic granuloma originating from the dura mater with secondary osseous invasion in an 11-year-old female child who presented with a swelling in the right parietal region. Magnetic resonance imaging demonstrated an enhancing mass with a wide dural attachment with a lytic lesion in the overlying skull. Right parietal extended craniotomy was done with the excision of mass from the dura. Histopathological features of mass were characteristic of eosinophilic granuloma which was confirmed by positive immunohistochemical staining for CD1a. Medknow Publications & Media Pvt Ltd 2017 /pmc/articles/PMC5652098/ /pubmed/29114286 http://dx.doi.org/10.4103/ajns.AJNS_47_15 Text en Copyright: © 2017 Asian Journal of Neurosurgery 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
Mardi, Kavita
Thakur, R. C.
Negi, Lalita
Intradural Eosinophilic Granuloma Invading Skull: Case Report and Review of the Literature
title Intradural Eosinophilic Granuloma Invading Skull: Case Report and Review of the Literature
title_full Intradural Eosinophilic Granuloma Invading Skull: Case Report and Review of the Literature
title_fullStr Intradural Eosinophilic Granuloma Invading Skull: Case Report and Review of the Literature
title_full_unstemmed Intradural Eosinophilic Granuloma Invading Skull: Case Report and Review of the Literature
title_short Intradural Eosinophilic Granuloma Invading Skull: Case Report and Review of the Literature
title_sort intradural eosinophilic granuloma invading skull: case report and review of the literature
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5652098/
https://www.ncbi.nlm.nih.gov/pubmed/29114286
http://dx.doi.org/10.4103/ajns.AJNS_47_15
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