Medulloblastoma: Clinicopathological Correlates of SHH, WNT, and Non-WNT/SHH Molecular Subgroups Analysis and Prognostic Significance: Mono-Institutional Series

dc.contributor.authorHasbay, Bermal
dc.contributor.authorKayaselcuk, Fazilet
dc.contributor.authorSuner, Halil Ibrahim
dc.contributor.authorSarialioglu, Faik
dc.contributor.orcIDhttps://orcid.org/0000-0002-5957-8611en_US
dc.contributor.pubmedID000832603900001en_US
dc.contributor.researcherIDAAJ-5381-2021en_US
dc.date.accessioned2022-12-21T08:23:44Z
dc.date.available2022-12-21T08:23:44Z
dc.date.issued2022
dc.description.abstractAIM: To reevaluate the medulloblastoma cases according to histomorphological and molecular features, and to investigate the relationship between the prognostic factors of the new WHO classification by applying Beta-catenin, YAP1, GAP1, p53, and INI1 antibodies immunohistochemically. MATERIAL and METHODS: This study includes 41 patients who have been diagnosed with medulloblastoma between 2007-2019 in pathology department. Immunohistochemically, p53, beta-catenin, YAP1, GAP1, and INI1 immune markers were applied, and the relationship between the results and the prognostic parameters was evaluated statistically. RESULTS: When 41 patients were classified into WHO medulloblastoma histological subtype groups according to histomorphological features, 22 (53.7%) patients were classified as classical type, 11 (26.8%) patients as desmoplastic nodular type, and 8 (19.5%) patients as large cell/anaplastic type medulloblastoma. According to their molecular characteristics, 14 (34.1%) patients were in the Non-WNT/SHH group, 5 (12.2%) patients were SHH mutant, 17 (41.5%) patients were SHH wild, and 5 (12.2%) patients were in the WNT active group. There was no statistically significant correlation between age, gender, tumor size, recurrence, Ki67 proliferation index with molecular types and histopathological types. CONCLUSION: In our study, metastasis at the time of diagnosis, histological large cell anaplastic type, immunohistochemical p53 positivity, molecular SHH mutant type were the statistically significant indicators of worse prognosis and shorter survival time.en_US
dc.identifier.endpage602en_US
dc.identifier.issn1019-5149en_US
dc.identifier.issue4en_US
dc.identifier.scopus2-s2.0-85135373680en_US
dc.identifier.startpage595en_US
dc.identifier.urihttp://www.turkishneurosurgery.org.tr/pdf/pdf_JTN_2654.pdf
dc.identifier.urihttp://hdl.handle.net/11727/8394
dc.identifier.volume32en_US
dc.identifier.wos000832603900001en_US
dc.language.isoengen_US
dc.relation.isversionof10.5137/1019-5149.JTN.34490-21.3en_US
dc.relation.journalTURKISH NEUROSURGERYen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergien_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subjectMedulloblastomaen_US
dc.subjectHistological subtypeen_US
dc.subjectMolecular characteristicen_US
dc.subjectImmunohistochemistryen_US
dc.titleMedulloblastoma: Clinicopathological Correlates of SHH, WNT, and Non-WNT/SHH Molecular Subgroups Analysis and Prognostic Significance: Mono-Institutional Seriesen_US
dc.typeArticleen_US

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