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Please use this identifier to cite or link to this item: http://repository.li.mahidol.ac.th/dspace/handle/123456789/73830
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dc.contributor.authorPoramate Pitak-Arnnopen_US
dc.contributor.authorKeskanya Subbalekhaen_US
dc.contributor.authorNattapong Sirintawaten_US
dc.contributor.authorJean Paul Meningauden_US
dc.contributor.authorChatpong Tangmaneeen_US
dc.contributor.authorPrim Auychaien_US
dc.contributor.authorAndreas Neffen_US
dc.contributor.otherChulalongkorn Business Schoolen_US
dc.contributor.otherMahidol University, Faculty of Dentistryen_US
dc.contributor.otherChulalongkorn Universityen_US
dc.contributor.otherHôpital Henri Mondoren_US
dc.contributor.otherUniversitätsklinikum Gießen und Marburg, Standort Marburgen_US
dc.date.accessioned2022-08-04T03:55:55Z-
dc.date.available2022-08-04T03:55:55Z-
dc.date.issued2022-01-01en_US
dc.identifier.citationJournal of Stomatology, Oral and Maxillofacial Surgery. (2022)en_US
dc.identifier.issn24687855en_US
dc.identifier.other2-s2.0-85127340515en_US
dc.identifier.urihttp://repository.li.mahidol.ac.th/dspace/handle/123456789/73830-
dc.description.abstractPurpose: To identify factors associated with skull base involvement (SBI) of maxillary ameloblastomas (MA). Methods: This retrospective cohort study was composed of MA patients treated during a 7-year period. Demographic, radiographic, and nine immunohistopathologic predictor variables were included. The outcome variable was presence of SBI (yes/no). Descriptive, bi- and multivariate statistics were computed, and P ≤ .05 in multivariate analyses was considered statistically significant. Results: The sample comprised 23 subjects (34.8% females; 21.7% with SBI) with a mean age of 50.3 ± 18.2 years. Candidate predictors of an SBI in MAs were 1) male gender, 2) a low Karnofsky Performance Status score (KPS), 3) multilocular radiolucency, 4) ill-defined margins, 5) cortical perforation, 6) inclusion of an unerupted tooth, 7) moderate to strong reactivity to p53, Ki-67, CD10, astrocyte elevated gene-1 (AEG-1) protein, carbonic anhydrase IX (CA IX), calretinin (calbindin2; CALB2), and BRAF-V600E, and 8) negative to low immunopositivity to α-smooth muscle actin (α-SMA) and syndecan-1 (CD138). However, multivariate analyses confirmed the significant associations of SBI with negative/low syndecan-1 reactivity (P = .003; adjusted odds ratio [ORadj.], 4.04; 95% confidence interval [95% CI], −.89 to −.48; Pearson's Correlation Coefficient [r] = −.74) and with KPS (P = .003; ORadj., 4.04; 95% CI, −.78 to −.17; r = −.54) only. Conclusions: Our findings suggest an aggressive approach to MAs with negative to low syndecan-1 immunopositivity and/or in multi-morbid patients (who may have difficulty in access to health care). Otherwise, health care inequalities due to low KPS scores should be minimized or eliminated.en_US
dc.rightsMahidol Universityen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85127340515&origin=inwarden_US
dc.subjectDentistryen_US
dc.subjectMedicineen_US
dc.titleA retrospective cohort study on predictors associated with skull base invasion of maxillary ameloblastomasen_US
dc.typeArticleen_US
dc.rights.holderSCOPUSen_US
dc.identifier.doi10.1016/j.jormas.2022.03.015en_US
dc.identifier.urlhttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85127340515&origin=inwarden_US
Appears in Collections:Scopus 2022

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