Bilateral Meningioma: A Case Report and Review of the Literature

Here, we present a rarely seen example of bilateral meningiomas exhibiting different malignancy grades, I (meningothelial) and II (atypical), recorded in a 72-year-old patient. The presence of two separated lesions of different grades in a single patient can elucidate meningioma progression. To this...

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Main Authors: Anja Bukovac, Hana Panić, Tomislava Mrgan, Nika Šlaus, Anja Kafka, Niko Njirić, Nives Pećina-Šlaus
Format: Article
Language:English
Published: MDPI AG 2022-01-01
Series:International Journal of Molecular Sciences
Subjects:
Online Access:https://www.mdpi.com/1422-0067/23/3/1187
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author Anja Bukovac
Hana Panić
Tomislava Mrgan
Nika Šlaus
Anja Kafka
Niko Njirić
Nives Pećina-Šlaus
author_facet Anja Bukovac
Hana Panić
Tomislava Mrgan
Nika Šlaus
Anja Kafka
Niko Njirić
Nives Pećina-Šlaus
author_sort Anja Bukovac
collection DOAJ
description Here, we present a rarely seen example of bilateral meningiomas exhibiting different malignancy grades, I (meningothelial) and II (atypical), recorded in a 72-year-old patient. The presence of two separated lesions of different grades in a single patient can elucidate meningioma progression. To this end, the involvement of specific protein markers of epithelial to mesenchymal transition (EMT), the process responsible for progression, was tested in both tumors. Protein expression status of specific epithelial (E-cadherin) and mesenchymal markers (N-cadherin, SNAIL&SLUG and TWIST1) was investigated. Furthermore, markers that are connected to Wnt signaling pathway–beta-catenin, GSK3beta and DVL1—were also analyzed. For signs of neurofibromatosis and schwanomatosis genetic testing was performed. Immunohistochemistry evaluated by immunoreactivity score (IRS) was used to determine the signal strengths and proteins’ location. Our results indicated that, in comparison to the grade I tumor, mesenchymal markers SNAIL and SLUG were upregulated in the atypical meningioma. TWIST1, beta-catenin and GSK3beta were upregulated in both grades, while E-cadherin was partially lost. A pronounced cadherin switch could not be established; however, N-cadherin showed widespread tissue presence. Genetic testing did not detect changes of <i>NF2</i> or <i>SMARCB1</i> genes denying germline origin of the lesions. The rare presence of two different grades in one patient elucidate previously unknown molecules involved in meningioma progression.
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spelling doaj.art-166230a7df4740b88a1f5cbbaf34c7412023-11-23T16:36:21ZengMDPI AGInternational Journal of Molecular Sciences1661-65961422-00672022-01-01233118710.3390/ijms23031187Bilateral Meningioma: A Case Report and Review of the LiteratureAnja Bukovac0Hana Panić1Tomislava Mrgan2Nika Šlaus3Anja Kafka4Niko Njirić5Nives Pećina-Šlaus6Laboratory of Neuro-Oncology, Croatian Institute for Brain Research, School of Medicine, University of Zagreb, Šalata 12, 10000 Zagreb, CroatiaSchool of Medicine, University of Zagreb, Šalata 3, 10000 Zagreb, CroatiaSchool of Medicine, University of Zagreb, Šalata 3, 10000 Zagreb, CroatiaSchool of Medicine, University of Zagreb, Šalata 3, 10000 Zagreb, CroatiaLaboratory of Neuro-Oncology, Croatian Institute for Brain Research, School of Medicine, University of Zagreb, Šalata 12, 10000 Zagreb, CroatiaDepartment of Neurosurgery, University Hospital Center “Zagreb”, School of Medicine, University of Zagreb, Kišpatićeva 12, 10000 Zagreb, CroatiaLaboratory of Neuro-Oncology, Croatian Institute for Brain Research, School of Medicine, University of Zagreb, Šalata 12, 10000 Zagreb, CroatiaHere, we present a rarely seen example of bilateral meningiomas exhibiting different malignancy grades, I (meningothelial) and II (atypical), recorded in a 72-year-old patient. The presence of two separated lesions of different grades in a single patient can elucidate meningioma progression. To this end, the involvement of specific protein markers of epithelial to mesenchymal transition (EMT), the process responsible for progression, was tested in both tumors. Protein expression status of specific epithelial (E-cadherin) and mesenchymal markers (N-cadherin, SNAIL&SLUG and TWIST1) was investigated. Furthermore, markers that are connected to Wnt signaling pathway–beta-catenin, GSK3beta and DVL1—were also analyzed. For signs of neurofibromatosis and schwanomatosis genetic testing was performed. Immunohistochemistry evaluated by immunoreactivity score (IRS) was used to determine the signal strengths and proteins’ location. Our results indicated that, in comparison to the grade I tumor, mesenchymal markers SNAIL and SLUG were upregulated in the atypical meningioma. TWIST1, beta-catenin and GSK3beta were upregulated in both grades, while E-cadherin was partially lost. A pronounced cadherin switch could not be established; however, N-cadherin showed widespread tissue presence. Genetic testing did not detect changes of <i>NF2</i> or <i>SMARCB1</i> genes denying germline origin of the lesions. The rare presence of two different grades in one patient elucidate previously unknown molecules involved in meningioma progression.https://www.mdpi.com/1422-0067/23/3/1187multiple meningiomabilateral meningiomaEMTWnt signalingE-cadherinN-cadherin
spellingShingle Anja Bukovac
Hana Panić
Tomislava Mrgan
Nika Šlaus
Anja Kafka
Niko Njirić
Nives Pećina-Šlaus
Bilateral Meningioma: A Case Report and Review of the Literature
International Journal of Molecular Sciences
multiple meningioma
bilateral meningioma
EMT
Wnt signaling
E-cadherin
N-cadherin
title Bilateral Meningioma: A Case Report and Review of the Literature
title_full Bilateral Meningioma: A Case Report and Review of the Literature
title_fullStr Bilateral Meningioma: A Case Report and Review of the Literature
title_full_unstemmed Bilateral Meningioma: A Case Report and Review of the Literature
title_short Bilateral Meningioma: A Case Report and Review of the Literature
title_sort bilateral meningioma a case report and review of the literature
topic multiple meningioma
bilateral meningioma
EMT
Wnt signaling
E-cadherin
N-cadherin
url https://www.mdpi.com/1422-0067/23/3/1187
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