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Atrialised right ventricular myxoma in a patient with Ebstein’s anomaly

dc.contributor.authorJohn, T. J.en_ZA
dc.contributor.authorSnyman, H. W.en_ZA
dc.contributor.authorJanson, J.en_ZA
dc.contributor.authorPecoraro, A. J. K.en_ZA
dc.date.accessioned2019-09-17T08:27:08Z
dc.date.available2019-09-17T08:27:08Z
dc.date.issued2018
dc.identifier.citationJohn, T. J., et al. 2018. Atrialised right ventricular myxoma in a patient with Ebstein’s anomaly. Echo Research and Practice, 5(1):K23-K27, doi:10.1530/ERP-17-0065
dc.identifier.issn2055-0464 (online)
dc.identifier.otherdoi:10.1530/ERP-17-0065
dc.identifier.urihttp://hdl.handle.net/10019.1/106479
dc.descriptionCITATION: John, T. J., et al. 2018. Atrialised right ventricular myxoma in a patient with Ebstein’s anomaly. Echo Research and Practice, 5(1):K23-K27, doi:10.1530/ERP-17-0065.
dc.descriptionThe original publication is available at https://erp.bioscientifica.com
dc.description.abstractEbstein’s anomaly is a rare entity affecting around 1 in 200,000 live births and accounts for less than 1% of congenital heart diseases. Ebstein’s anomaly with an associated right-sided myxoma is extremely rare, with only one other case report found in the literature. Previous reports have also noted cases of Ebstein’s anomaly associated with left-sided myxomas. We describe a female patient with, to our knowledge, the first case of a histopathologically confirmed right ventricular myxoma in the setting of Ebstein’s anomaly.en_ZA
dc.description.urihttps://erp.bioscientifica.com/view/journals/echo/5/1/ERP-17-0065.xml
dc.format.extent5 pages
dc.language.isoen_ZAen_ZA
dc.publisherBioScientifica
dc.subjectMyxomaen_ZA
dc.subjectEbstein's anomalyen_ZA
dc.titleAtrialised right ventricular myxoma in a patient with Ebstein’s anomalyen_ZA
dc.typeArticleen_ZA
dc.description.versionPublisher's version
dc.rights.holderAuthors retain copyright


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