Atypical presentation of polymorphous low-grade neuroepithelial tumor of young (PLNTY): a case report

Abstract The polymorphous low-grade neuroepithelial tumor of young (PLNTY) is considered as one among the low-grade neuroepithelial tumor; as per WHO-2021 classification of Brain Tumors in the fifth edition. The term PLNTY was first coined by Huse in 2016. These morphologically variable tumors are c...

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Main Authors: Vijay Joshi, Meghana V. Chougule, Anand Mudkanna, Rakesh Kumar Mishra, Ved Prakash Maurya, Amit Agrawal
Format: Article
Language:English
Published: SpringerOpen 2023-02-01
Series:Egyptian Journal of Neurosurgery
Subjects:
Online Access:https://doi.org/10.1186/s41984-023-00192-2
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author Vijay Joshi
Meghana V. Chougule
Anand Mudkanna
Rakesh Kumar Mishra
Ved Prakash Maurya
Amit Agrawal
author_facet Vijay Joshi
Meghana V. Chougule
Anand Mudkanna
Rakesh Kumar Mishra
Ved Prakash Maurya
Amit Agrawal
author_sort Vijay Joshi
collection DOAJ
description Abstract The polymorphous low-grade neuroepithelial tumor of young (PLNTY) is considered as one among the low-grade neuroepithelial tumor; as per WHO-2021 classification of Brain Tumors in the fifth edition. The term PLNTY was first coined by Huse in 2016. These morphologically variable tumors are characterized by their oligodendroglioma-like cellular components, infiltrative growth pattern, and Cluster of Differentiation 34 (CD34) immunopositivity. Frequent genetic abnormalities involving mitogen-activated protein kinase pathway constituents like the BRAF proto-oncogene or fibroblast growth receptor 2/3 are harbored by PLNTYs. Radiologically, these are found to be well-circumscribed lesions with calcified and cystic components, affecting primarily temporal lobes. Clinically, they present with seizures/epilepsy in young adults (< 30 years). In the present manuscript we are reporting a case of 37-year-old male, presenting with a gradually progressive headache for 6 months, found to have a left frontal multiloculated cystic lesion with dystrophic calcifications. Based on the distinctive histopathological feature of the oligodendroglioma-like infiltrative lesion showing CD34 immunopositivity, a diagnosis of a polymorphous low-grade neuroepithelial tumor of young was made.
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spelling doaj.art-a1391c466ce5419d87518fcd881d48912023-03-22T10:42:06ZengSpringerOpenEgyptian Journal of Neurosurgery2520-82252023-02-013811610.1186/s41984-023-00192-2Atypical presentation of polymorphous low-grade neuroepithelial tumor of young (PLNTY): a case reportVijay Joshi0Meghana V. Chougule1Anand Mudkanna2Rakesh Kumar Mishra3Ved Prakash Maurya4Amit Agrawal5Sparsh Neuro and Superspeciality HospitalShant Pathology Laboratory and Cancer Diagnosis CentreSparsh Neuro and Superspeciality HospitalDepartment of Neurosurgery, Institute of Medical Sciences, Trauma Centre and Mahamana Centenary Superspeciality Hospital, Banaras Hindu UniversityDepartment of Neurosurgery, SGPGIMSDepartment of Neurosurgery, All India Institute of Medical SciencesAbstract The polymorphous low-grade neuroepithelial tumor of young (PLNTY) is considered as one among the low-grade neuroepithelial tumor; as per WHO-2021 classification of Brain Tumors in the fifth edition. The term PLNTY was first coined by Huse in 2016. These morphologically variable tumors are characterized by their oligodendroglioma-like cellular components, infiltrative growth pattern, and Cluster of Differentiation 34 (CD34) immunopositivity. Frequent genetic abnormalities involving mitogen-activated protein kinase pathway constituents like the BRAF proto-oncogene or fibroblast growth receptor 2/3 are harbored by PLNTYs. Radiologically, these are found to be well-circumscribed lesions with calcified and cystic components, affecting primarily temporal lobes. Clinically, they present with seizures/epilepsy in young adults (< 30 years). In the present manuscript we are reporting a case of 37-year-old male, presenting with a gradually progressive headache for 6 months, found to have a left frontal multiloculated cystic lesion with dystrophic calcifications. Based on the distinctive histopathological feature of the oligodendroglioma-like infiltrative lesion showing CD34 immunopositivity, a diagnosis of a polymorphous low-grade neuroepithelial tumor of young was made.https://doi.org/10.1186/s41984-023-00192-2Polymorphous low-grade neuroepithelial tumor of youngPLNTYCD34MAPK pathwayLow-grade epilepsy-associated tumors
spellingShingle Vijay Joshi
Meghana V. Chougule
Anand Mudkanna
Rakesh Kumar Mishra
Ved Prakash Maurya
Amit Agrawal
Atypical presentation of polymorphous low-grade neuroepithelial tumor of young (PLNTY): a case report
Egyptian Journal of Neurosurgery
Polymorphous low-grade neuroepithelial tumor of young
PLNTY
CD34
MAPK pathway
Low-grade epilepsy-associated tumors
title Atypical presentation of polymorphous low-grade neuroepithelial tumor of young (PLNTY): a case report
title_full Atypical presentation of polymorphous low-grade neuroepithelial tumor of young (PLNTY): a case report
title_fullStr Atypical presentation of polymorphous low-grade neuroepithelial tumor of young (PLNTY): a case report
title_full_unstemmed Atypical presentation of polymorphous low-grade neuroepithelial tumor of young (PLNTY): a case report
title_short Atypical presentation of polymorphous low-grade neuroepithelial tumor of young (PLNTY): a case report
title_sort atypical presentation of polymorphous low grade neuroepithelial tumor of young plnty a case report
topic Polymorphous low-grade neuroepithelial tumor of young
PLNTY
CD34
MAPK pathway
Low-grade epilepsy-associated tumors
url https://doi.org/10.1186/s41984-023-00192-2
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