Pleomorphic xanthoastrocytoma with anaplastic features: A case report

Pleomorphic xanthoastrocytoma has been considered as an astrocytic tumor with relatively favorable prognosis. It corresponds to WHO Grade-II neoplasm. Recently, several patterns with relatively poor prognosis have been recorded and a new concept of "PXA with anaplastic features" has been p...

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Main Authors: Sadiya Niamathullah, S Sivaselvam, Mitra Ghosh, Siddhartha Ghosh
Format: Article
Language:English
Published: Wolters Kluwer Medknow Publications 2014-01-01
Series:Indian Journal of Pathology and Microbiology
Subjects:
Online Access:http://www.ijpmonline.org/article.asp?issn=0377-4929;year=2014;volume=57;issue=1;spage=101;epage=104;aulast=Niamathullah
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author Sadiya Niamathullah
S Sivaselvam
Mitra Ghosh
Siddhartha Ghosh
author_facet Sadiya Niamathullah
S Sivaselvam
Mitra Ghosh
Siddhartha Ghosh
author_sort Sadiya Niamathullah
collection DOAJ
description Pleomorphic xanthoastrocytoma has been considered as an astrocytic tumor with relatively favorable prognosis. It corresponds to WHO Grade-II neoplasm. Recently, several patterns with relatively poor prognosis have been recorded and a new concept of "PXA with anaplastic features" has been proposed. The present case is about a 9-year-old girl who presented with symptoms of recurrent headache, seizures and poor academic performance. MRI revealed left fronto-parietal irregular enhancing mass lesion with callosal involvement and right mid-brain arteriovenous malformation. Clinical and radiological examination was suggestive of a high grade glial neoplasm/PNET. A diagnosis of high grade glial neoplasm was rendered on the squash smears submitted for frozen sections based on the presence of spindle cells, admixed with pleomorphic bizarre, giant cells with multilobated nuclei showing few atypical mitosis and abundant eosinophilic cytoplasm. Frontal craniotomy with debulking of the tumor was performed and permanent sections revealed a biphasic glial neoplasm with spindle cells arranged in fascicles admixed with bizarre multinucleated giant cells showing abundant vacuolated and lipidized cytoplasm, nuclear hyperchromasia with intranuclear inclusions. Eosinophilic granular bodies, mitosis of 7/10 HPF, micro vascular proliferation, necrosis and invasion into the underlying brain parenchyma were noted. With these histomorphological findings a diagnosis of pleomorphic xanthoastrocytoma with anaplastic features was rendered.
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spelling doaj.art-d0250c65c075478783188a67e23751cc2022-12-22T00:58:36ZengWolters Kluwer Medknow PublicationsIndian Journal of Pathology and Microbiology0377-49292014-01-0157110110410.4103/0377-4929.130913Pleomorphic xanthoastrocytoma with anaplastic features: A case reportSadiya NiamathullahS SivaselvamMitra GhoshSiddhartha GhoshPleomorphic xanthoastrocytoma has been considered as an astrocytic tumor with relatively favorable prognosis. It corresponds to WHO Grade-II neoplasm. Recently, several patterns with relatively poor prognosis have been recorded and a new concept of "PXA with anaplastic features" has been proposed. The present case is about a 9-year-old girl who presented with symptoms of recurrent headache, seizures and poor academic performance. MRI revealed left fronto-parietal irregular enhancing mass lesion with callosal involvement and right mid-brain arteriovenous malformation. Clinical and radiological examination was suggestive of a high grade glial neoplasm/PNET. A diagnosis of high grade glial neoplasm was rendered on the squash smears submitted for frozen sections based on the presence of spindle cells, admixed with pleomorphic bizarre, giant cells with multilobated nuclei showing few atypical mitosis and abundant eosinophilic cytoplasm. Frontal craniotomy with debulking of the tumor was performed and permanent sections revealed a biphasic glial neoplasm with spindle cells arranged in fascicles admixed with bizarre multinucleated giant cells showing abundant vacuolated and lipidized cytoplasm, nuclear hyperchromasia with intranuclear inclusions. Eosinophilic granular bodies, mitosis of 7/10 HPF, micro vascular proliferation, necrosis and invasion into the underlying brain parenchyma were noted. With these histomorphological findings a diagnosis of pleomorphic xanthoastrocytoma with anaplastic features was rendered.http://www.ijpmonline.org/article.asp?issn=0377-4929;year=2014;volume=57;issue=1;spage=101;epage=104;aulast=NiamathullahAnaplastic featuresastrocytic tumorpleomorphic xanthoastrocytoma
spellingShingle Sadiya Niamathullah
S Sivaselvam
Mitra Ghosh
Siddhartha Ghosh
Pleomorphic xanthoastrocytoma with anaplastic features: A case report
Indian Journal of Pathology and Microbiology
Anaplastic features
astrocytic tumor
pleomorphic xanthoastrocytoma
title Pleomorphic xanthoastrocytoma with anaplastic features: A case report
title_full Pleomorphic xanthoastrocytoma with anaplastic features: A case report
title_fullStr Pleomorphic xanthoastrocytoma with anaplastic features: A case report
title_full_unstemmed Pleomorphic xanthoastrocytoma with anaplastic features: A case report
title_short Pleomorphic xanthoastrocytoma with anaplastic features: A case report
title_sort pleomorphic xanthoastrocytoma with anaplastic features a case report
topic Anaplastic features
astrocytic tumor
pleomorphic xanthoastrocytoma
url http://www.ijpmonline.org/article.asp?issn=0377-4929;year=2014;volume=57;issue=1;spage=101;epage=104;aulast=Niamathullah
work_keys_str_mv AT sadiyaniamathullah pleomorphicxanthoastrocytomawithanaplasticfeaturesacasereport
AT ssivaselvam pleomorphicxanthoastrocytomawithanaplasticfeaturesacasereport
AT mitraghosh pleomorphicxanthoastrocytomawithanaplasticfeaturesacasereport
AT siddharthaghosh pleomorphicxanthoastrocytomawithanaplasticfeaturesacasereport