A rare cardiac tumor in childhood: Right atrial myxoma; [Çocuk yaş grubunda nadir bir kardiyak tümör: Saǧ atriyal miksoma]

dc.contributor.authorKurdal A.T.
dc.contributor.authorEserdaǧ M.
dc.contributor.authorIşkesen I.
dc.contributor.authorŞirin B.H.
dc.date.accessioned2024-07-22T08:20:08Z
dc.date.available2024-07-22T08:20:08Z
dc.date.issued2011
dc.description.abstractMyxoma is a rare tumor in childhood and unlike left atrial localization is quite rare in right atrium. A 14-year-old male child presented with complains of exertional dys-pnea and tachycardia. Transthoracic echocardiography revealed a huge myxoma in the right atrium, closing the inferior vena cava orifice and causing tricuspid stenosis. Cardiopulmonary bypass was started only with superior vena cava cannulation. Inferior vena cava cannulation was performed after cardiac arrest due to the embolic risk. The total resection was performed by right atriotomy.
dc.identifier.issn13015680
dc.identifier.urihttp://akademikarsiv.cbu.edu.tr:4000/handle/123456789/18012
dc.language.isoTurkish
dc.titleA rare cardiac tumor in childhood: Right atrial myxoma; [Çocuk yaş grubunda nadir bir kardiyak tümör: Saǧ atriyal miksoma]
dc.typeArticle

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