Recurrent multi-cameral cardiac myxomas in a child with Carney complex

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dc.contributor.authorOscar Ballivián Burgos
dc.contributor.authorEricka Perez Albrecht
dc.contributor.authorJesus Pozo Robles
dc.contributor.authorRaquel Barron Mondaca
dc.contributor.authorRodrigo Soto
dc.contributor.authorTom R. Karl
dc.coverage.spatialBolivia
dc.date.accessioned2026-03-22T15:14:35Z
dc.date.available2026-03-22T15:14:35Z
dc.date.issued2023
dc.descriptionCitaciones: 4
dc.description.abstractCardiac myxoma is a relatively rare tumour, usually solitary, that occurs primarily in the left atrium of adults, but comprises only 30% of cardiac tumours in children. We recently treated a 12-year-old girl with multiple recurrent myxomas in three cardiac chambers(following surgical resection 3 years earlier). Genomic analysis showed the PKAR1A mutation typical for Carney complex.
dc.identifier.doi10.1017/s1047951122003961
dc.identifier.urihttps://doi.org/10.1017/s1047951122003961
dc.identifier.urihttps://andeanlibrary.org/handle/123456789/51221
dc.language.isoen
dc.publisherCambridge University Press
dc.relation.ispartofCardiology in the Young
dc.sourceMinisterio de Salud
dc.subjectMedicine
dc.subjectCarney complex
dc.subjectMyxoma
dc.subjectLeft atrium
dc.subjectGirl
dc.subjectResection
dc.subjectHeart neoplasms
dc.subjectSurgical resection
dc.subjectMutation
dc.subjectInternal medicine
dc.titleRecurrent multi-cameral cardiac myxomas in a child with Carney complex
dc.typearticle

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