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Multicystic oligodendroglioma with calvarial destruction

CONTEXT: Calvarial erosion is known to occur with some superficially located tumors. Very few case reports of calvarial erosion associated with oligodendroglioma are reported in the literature, but calvarial destruction with oligodendroglioma is very rare. AIM: To report an unusual case of multicyst...

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Autor principal: Bajaj, Ajay
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4129584/
https://www.ncbi.nlm.nih.gov/pubmed/25126125
http://dx.doi.org/10.4103/1793-5482.136723
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author Bajaj, Ajay
author_facet Bajaj, Ajay
author_sort Bajaj, Ajay
collection PubMed
description CONTEXT: Calvarial erosion is known to occur with some superficially located tumors. Very few case reports of calvarial erosion associated with oligodendroglioma are reported in the literature, but calvarial destruction with oligodendroglioma is very rare. AIM: To report an unusual case of multicystic frontoparietal oligodendroglioma with destruction of the calvaria and scalp involvement in the absence of prior surgery or radiation. MATERIALS AND METHODS: A 30-year-old male presented with the history of left focal seizure with secondary generalization for last three to four years along with left sided weakness for the past one month. There was history of slowly progressive decreased vision in both eyes leading to complete blindness in both eyes for the past one month. On neurological examination, patient had left hemiparesis of grade-2/5 with perception of light absent in both eyes. Fundus examination revealed bilateral optic atrophy. Magnetic resonance imaging (MRI) of the brain showed a large supratentorial heterogenous multicystic ring enhancing mass lesion involving right frontal lobe, right frontotemporal opercular region, and posteriorly abutting the central sulcus and anteriorly destroying the calvaria. Patient underwent right frontoparietal craniotomy and near total excision of tumor. Histopathological examination revealed oligodendroglioma WHO grade-2. Patient received postoperative chemoradiotherapy. RESULTS: At nine month follow-up patient neurological status was same and his seizure was controlled on single AED. There was no recurrence of seizure at nine month of follow-up. CONCLUSIONS: Calvarial destruction in association with extra and intra axial neoplasm should include oligodendroglioma especially in patients with long history of symptoms, although calvarial destruction is very rare. However, the final diagnosis is established by means of histopathological examination.
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spelling pubmed-41295842014-08-14 Multicystic oligodendroglioma with calvarial destruction Bajaj, Ajay Asian J Neurosurg Case Report CONTEXT: Calvarial erosion is known to occur with some superficially located tumors. Very few case reports of calvarial erosion associated with oligodendroglioma are reported in the literature, but calvarial destruction with oligodendroglioma is very rare. AIM: To report an unusual case of multicystic frontoparietal oligodendroglioma with destruction of the calvaria and scalp involvement in the absence of prior surgery or radiation. MATERIALS AND METHODS: A 30-year-old male presented with the history of left focal seizure with secondary generalization for last three to four years along with left sided weakness for the past one month. There was history of slowly progressive decreased vision in both eyes leading to complete blindness in both eyes for the past one month. On neurological examination, patient had left hemiparesis of grade-2/5 with perception of light absent in both eyes. Fundus examination revealed bilateral optic atrophy. Magnetic resonance imaging (MRI) of the brain showed a large supratentorial heterogenous multicystic ring enhancing mass lesion involving right frontal lobe, right frontotemporal opercular region, and posteriorly abutting the central sulcus and anteriorly destroying the calvaria. Patient underwent right frontoparietal craniotomy and near total excision of tumor. Histopathological examination revealed oligodendroglioma WHO grade-2. Patient received postoperative chemoradiotherapy. RESULTS: At nine month follow-up patient neurological status was same and his seizure was controlled on single AED. There was no recurrence of seizure at nine month of follow-up. CONCLUSIONS: Calvarial destruction in association with extra and intra axial neoplasm should include oligodendroglioma especially in patients with long history of symptoms, although calvarial destruction is very rare. However, the final diagnosis is established by means of histopathological examination. Medknow Publications & Media Pvt Ltd 2014 /pmc/articles/PMC4129584/ /pubmed/25126125 http://dx.doi.org/10.4103/1793-5482.136723 Text en Copyright: © 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-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
Bajaj, Ajay
Multicystic oligodendroglioma with calvarial destruction
title Multicystic oligodendroglioma with calvarial destruction
title_full Multicystic oligodendroglioma with calvarial destruction
title_fullStr Multicystic oligodendroglioma with calvarial destruction
title_full_unstemmed Multicystic oligodendroglioma with calvarial destruction
title_short Multicystic oligodendroglioma with calvarial destruction
title_sort multicystic oligodendroglioma with calvarial destruction
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4129584/
https://www.ncbi.nlm.nih.gov/pubmed/25126125
http://dx.doi.org/10.4103/1793-5482.136723
work_keys_str_mv AT bajajajay multicysticoligodendrogliomawithcalvarialdestruction