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Lymphoplasmacyte-rich meningioma with atypical cystic-solid feature: A case report
BACKGROUND: Lymphoplasmacyte-rich meningioma (LPRM) is one of the rarest variants of meningioma and is classified as grade I (benign) tumor. It is characterized by abundant infiltrates of lymphocytes and plasma cells. Here, we report an extremely rare case of LPRM with an atypical imaging finding of...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Baishideng Publishing Group Inc
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7520769/ https://www.ncbi.nlm.nih.gov/pubmed/33024789 http://dx.doi.org/10.12998/wjcc.v8.i18.4272 |
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author | Gu, Kang-Chen Wan, Yang Xiang, Li Wang, Long-Sheng Yao, Wen-Jun |
author_facet | Gu, Kang-Chen Wan, Yang Xiang, Li Wang, Long-Sheng Yao, Wen-Jun |
author_sort | Gu, Kang-Chen |
collection | PubMed |
description | BACKGROUND: Lymphoplasmacyte-rich meningioma (LPRM) is one of the rarest variants of meningioma and is classified as grade I (benign) tumor. It is characterized by abundant infiltrates of lymphocytes and plasma cells. Here, we report an extremely rare case of LPRM with an atypical imaging finding of multiple cysts around a solid mass. CASE SUMMARY: The patient was a 36-year-old man with intermittent headache, dizziness, and vomiting for 2 years. Computed tomography and magnetic resonance imaging presented a cystic solid mass in the right frontal lobe with heavy peritumoral edema and obvious contrast enhancement. The patient was treated with right frontotemporal craniotomy, and gross total resection of the tumor was achieved without adjuvant therapy. There was no clinical or neuroradiological evidence of recurrent or residual tumor for 3 years after initial surgery. CONCLUSION: LPRM is one of the rarest variants of meningioma. Although, the mass of this case had common features, multiple cysts with nonuniform size and thin wall around the solid part are uncommon imaging finding, increasing the rate of misdiagnosis. The definitive diagnosis of LPRM relies on histopathological findings. |
format | Online Article Text |
id | pubmed-7520769 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Baishideng Publishing Group Inc |
record_format | MEDLINE/PubMed |
spelling | pubmed-75207692020-10-05 Lymphoplasmacyte-rich meningioma with atypical cystic-solid feature: A case report Gu, Kang-Chen Wan, Yang Xiang, Li Wang, Long-Sheng Yao, Wen-Jun World J Clin Cases Case Report BACKGROUND: Lymphoplasmacyte-rich meningioma (LPRM) is one of the rarest variants of meningioma and is classified as grade I (benign) tumor. It is characterized by abundant infiltrates of lymphocytes and plasma cells. Here, we report an extremely rare case of LPRM with an atypical imaging finding of multiple cysts around a solid mass. CASE SUMMARY: The patient was a 36-year-old man with intermittent headache, dizziness, and vomiting for 2 years. Computed tomography and magnetic resonance imaging presented a cystic solid mass in the right frontal lobe with heavy peritumoral edema and obvious contrast enhancement. The patient was treated with right frontotemporal craniotomy, and gross total resection of the tumor was achieved without adjuvant therapy. There was no clinical or neuroradiological evidence of recurrent or residual tumor for 3 years after initial surgery. CONCLUSION: LPRM is one of the rarest variants of meningioma. Although, the mass of this case had common features, multiple cysts with nonuniform size and thin wall around the solid part are uncommon imaging finding, increasing the rate of misdiagnosis. The definitive diagnosis of LPRM relies on histopathological findings. Baishideng Publishing Group Inc 2020-09-26 2020-09-26 /pmc/articles/PMC7520769/ /pubmed/33024789 http://dx.doi.org/10.12998/wjcc.v8.i18.4272 Text en ©The Author(s) 2020. Published by Baishideng Publishing Group Inc. All rights reserved. http://creativecommons.org/licenses/by-nc/4.0/ This article is an open-access article which was selected by an in-house editor and fully peer-reviewed by external reviewers. It is distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. |
spellingShingle | Case Report Gu, Kang-Chen Wan, Yang Xiang, Li Wang, Long-Sheng Yao, Wen-Jun Lymphoplasmacyte-rich meningioma with atypical cystic-solid feature: A case report |
title | Lymphoplasmacyte-rich meningioma with atypical cystic-solid feature: A case report |
title_full | Lymphoplasmacyte-rich meningioma with atypical cystic-solid feature: A case report |
title_fullStr | Lymphoplasmacyte-rich meningioma with atypical cystic-solid feature: A case report |
title_full_unstemmed | Lymphoplasmacyte-rich meningioma with atypical cystic-solid feature: A case report |
title_short | Lymphoplasmacyte-rich meningioma with atypical cystic-solid feature: A case report |
title_sort | lymphoplasmacyte-rich meningioma with atypical cystic-solid feature: a case report |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7520769/ https://www.ncbi.nlm.nih.gov/pubmed/33024789 http://dx.doi.org/10.12998/wjcc.v8.i18.4272 |
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