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Rabdomiomas cardiacos múltiples, diagnóstico prenatal. Reporte de casos

Cardiac tumors are rare in children, having a maximum reported incidence of 0.027% in prenatal diagnosis, increasing the incidence in necropsy diagnosis; rhabdomyomas are the most frequent cardiac tumors, some cases are associated with tuberous sclerosis. We present the report of two cases in our un...

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Autores principales: Carrillo-Lima, Tania, Pacheco-López, Sandra L., Castro-Santiago, Paola L., Oseguera-Torres, Luis F.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Permanyer Publications 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8771041/
https://www.ncbi.nlm.nih.gov/pubmed/33621220
http://dx.doi.org/10.24875/ACM.200002031
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author Carrillo-Lima, Tania
Pacheco-López, Sandra L.
Castro-Santiago, Paola L.
Oseguera-Torres, Luis F.
author_facet Carrillo-Lima, Tania
Pacheco-López, Sandra L.
Castro-Santiago, Paola L.
Oseguera-Torres, Luis F.
author_sort Carrillo-Lima, Tania
collection PubMed
description Cardiac tumors are rare in children, having a maximum reported incidence of 0.027% in prenatal diagnosis, increasing the incidence in necropsy diagnosis; rhabdomyomas are the most frequent cardiac tumors, some cases are associated with tuberous sclerosis. We present the report of two cases in our unit that were diagnosed prenatal with follow-up after birth and one of them was associated with tuberous sclerosis. Both cases were admitted in a third level center, uncomplicated, without requiring surgical treatment, and could be discharged.
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spelling pubmed-87710412022-01-24 Rabdomiomas cardiacos múltiples, diagnóstico prenatal. Reporte de casos Carrillo-Lima, Tania Pacheco-López, Sandra L. Castro-Santiago, Paola L. Oseguera-Torres, Luis F. Arch Cardiol Mex Artículo Especial Cardiac tumors are rare in children, having a maximum reported incidence of 0.027% in prenatal diagnosis, increasing the incidence in necropsy diagnosis; rhabdomyomas are the most frequent cardiac tumors, some cases are associated with tuberous sclerosis. We present the report of two cases in our unit that were diagnosed prenatal with follow-up after birth and one of them was associated with tuberous sclerosis. Both cases were admitted in a third level center, uncomplicated, without requiring surgical treatment, and could be discharged. Permanyer Publications 2022 2021-02-23 /pmc/articles/PMC8771041/ /pubmed/33621220 http://dx.doi.org/10.24875/ACM.200002031 Text en Copyright: © 2022 Permanyer https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License
spellingShingle Artículo Especial
Carrillo-Lima, Tania
Pacheco-López, Sandra L.
Castro-Santiago, Paola L.
Oseguera-Torres, Luis F.
Rabdomiomas cardiacos múltiples, diagnóstico prenatal. Reporte de casos
title Rabdomiomas cardiacos múltiples, diagnóstico prenatal. Reporte de casos
title_full Rabdomiomas cardiacos múltiples, diagnóstico prenatal. Reporte de casos
title_fullStr Rabdomiomas cardiacos múltiples, diagnóstico prenatal. Reporte de casos
title_full_unstemmed Rabdomiomas cardiacos múltiples, diagnóstico prenatal. Reporte de casos
title_short Rabdomiomas cardiacos múltiples, diagnóstico prenatal. Reporte de casos
title_sort rabdomiomas cardiacos múltiples, diagnóstico prenatal. reporte de casos
topic Artículo Especial
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8771041/
https://www.ncbi.nlm.nih.gov/pubmed/33621220
http://dx.doi.org/10.24875/ACM.200002031
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