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Mitral Annular Tumors: Report of Two Cases in Childhood

dc.authorid Kutay, Veysel/0000-0002-5822-5259
dc.authorscopusid 6602259733
dc.authorscopusid 7005925621
dc.authorscopusid 55931157400
dc.authorwosid Ekim, Hasan/Aam-3084-2021
dc.contributor.author Kutay, V
dc.contributor.author Yakut, C
dc.contributor.author Ekim, H
dc.date.accessioned 2025-05-10T17:29:00Z
dc.date.available 2025-05-10T17:29:00Z
dc.date.issued 2006
dc.department T.C. Van Yüzüncü Yıl Üniversitesi en_US
dc.department-temp Yuzuncu Yil Univ, KVC Klin, TR-65200 Van, Turkey; Yuzuncu Yil Univ, Fac Med, Cardiovasc Surg Clin, Van, Turkey en_US
dc.description Kutay, Veysel/0000-0002-5822-5259 en_US
dc.description.abstract Primary tumors of the mitral valve are extremely rare especially in the pediatric age group; only a few cases have been reported previously. The clinical appearance of the tumor may mimic other pathological findings of heart structures or remain asymptomatic. We describe two different benign primary cardiac tumors, which were hemangioma and myxoma originating from the anterior annulus of the mitral valve and presenting with an unusual clinical course in two children. Both tumors were resected successfully with mitral valve conservation and there was no recurrence at 6-month and 1-year follow-ups. en_US
dc.description.woscitationindex Science Citation Index Expanded
dc.identifier.doi 10.1111/j.1540-8191.2006.00205.x
dc.identifier.endpage 194 en_US
dc.identifier.issn 0886-0440
dc.identifier.issn 1540-8191
dc.identifier.issue 2 en_US
dc.identifier.pmid 16492286
dc.identifier.scopus 2-s2.0-33645239631
dc.identifier.scopusquality Q3
dc.identifier.startpage 191 en_US
dc.identifier.uri https://doi.org/10.1111/j.1540-8191.2006.00205.x
dc.identifier.uri https://hdl.handle.net/20.500.14720/12209
dc.identifier.volume 21 en_US
dc.identifier.wos WOS:000235417200023
dc.identifier.wosquality Q3
dc.language.iso en en_US
dc.publisher Wiley en_US
dc.relation.publicationcategory Diğer en_US
dc.rights info:eu-repo/semantics/closedAccess en_US
dc.title Mitral Annular Tumors: Report of Two Cases in Childhood en_US
dc.type Editorial en_US

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