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CC BY-NC-ND 4.0 · Asian J Neurosurg 2016; 11(04): 448-449
DOI: 10.4103/1793-5482.145084
CASE REPORT

Lymphoplasmacyte-rich meningioma with invasion of bone: A case report and review of literature

Dhruba Kurmi
Department of Neurosurgery, SMS Medical College, Jaipur, Rajasthan
,
Achal Sharma
Department of Neurosurgery, SMS Medical College, Jaipur, Rajasthan
,
R Mittal
Department of Neurosurgery, SMS Medical College, Jaipur, Rajasthan
,
Shashi Singhvi
1   Department of Pathology, SMS Medical College, Jaipur, Rajasthan
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Lymphoplasmacyte-rich (LPR) meningioma is a rare variant of meningioma, which is characterized by conspicuous infiltration of plasma cells and lymphocytes and a variable proportion of meningothelial elements, and is classified as a grade I tumor in World Health Organization (WHO) classification of tumors of central nervous system. The origin and biological behavior of this rare variant of meningioma is still not clear. Till date, very few cases of LPR meningioma have been reported globally. Here, we are presenting a case of right parietal convexity LPR meningioma with invasion of bone in a 32-year-old male patient, who presented to us with complaints of focal seizures and weakness in left upper limb.

Key-words:

Grade I - invasive - lymphoplasmacyte-rich meningioma


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Artikel online veröffentlicht:
20. September 2022

© 2016. Asian Congress of Neurological Surgeons. This is an open access article published by Thieme under the terms of the Creative Commons Attribution-NonDerivative-NonCommercial License, permitting copying and reproduction so long as the original work is given appropriate credit. Contents may not be used for commercial purposes, or adapted, remixed, transformed or built upon. (https://creativecommons.org/licenses/by-nc-nd/4.0/)

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