Rapidly involuting congenital hemangioma, diagnosed prenatally with heart failure and posnatal follow up.

Objectives: Describe the clinical case of a RICH that was diagnosed in uterus, normally in obstetric ultrasounds they are often confused with arteriovenous malformations and other congenital tumors. The differential diagnosis of these entities is important, since they have a different evolution, pro...

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Autores principales: Santarelli, Agustina, Gimenez, María Candelaria, Salduna, María Dolores, Valente, Enrique
Formato: Artículo revista
Lenguaje:Español
Publicado: Universidad Nacional Córdoba. Facultad de Ciencias Médicas. Secretaria de Ciencia y Tecnología 2026
Materias:
tumor
hemangiomas
heart failure
hemangioma
insuficiencia cardiaca
Insuficiência Cardíaca
Acceso en línea:https://revistas.unc.edu.ar/index.php/med/article/view/44679
Aporte de:
Revista de la Facultad de Ciencias Médicas de Córdoba de Universidad Nacional de Córdoba
id I10-R327-article-44679
record_format ojs
institution Universidad Nacional de Córdoba
institution_str I-10
repository_str R-327
container_title_str Revista de la Facultad de Ciencias Médicas de Córdoba
language Español
format Artículo revista
topic tumor
hemangiomas
heart failure
tumor
hemangioma
insuficiencia cardiaca
Insuficiência Cardíaca
tumor
hemangioma
spellingShingle tumor
hemangiomas
heart failure
tumor
hemangioma
insuficiencia cardiaca
Insuficiência Cardíaca
tumor
hemangioma
Santarelli, Agustina
Gimenez, María Candelaria
Salduna, María Dolores
Valente, Enrique
Rapidly involuting congenital hemangioma, diagnosed prenatally with heart failure and posnatal follow up.
topic_facet tumor
hemangiomas
heart failure
tumor
hemangioma
insuficiencia cardiaca
Insuficiência Cardíaca
tumor
hemangioma
author Santarelli, Agustina
Gimenez, María Candelaria
Salduna, María Dolores
Valente, Enrique
author_facet Santarelli, Agustina
Gimenez, María Candelaria
Salduna, María Dolores
Valente, Enrique
author_sort Santarelli, Agustina
title Rapidly involuting congenital hemangioma, diagnosed prenatally with heart failure and posnatal follow up.
title_short Rapidly involuting congenital hemangioma, diagnosed prenatally with heart failure and posnatal follow up.
title_full Rapidly involuting congenital hemangioma, diagnosed prenatally with heart failure and posnatal follow up.
title_fullStr Rapidly involuting congenital hemangioma, diagnosed prenatally with heart failure and posnatal follow up.
title_full_unstemmed Rapidly involuting congenital hemangioma, diagnosed prenatally with heart failure and posnatal follow up.
title_sort rapidly involuting congenital hemangioma, diagnosed prenatally with heart failure and posnatal follow up.
description Objectives: Describe the clinical case of a RICH that was diagnosed in uterus, normally in obstetric ultrasounds they are often confused with arteriovenous malformations and other congenital tumors. The differential diagnosis of these entities is important, since they have a different evolution, prognosis and treatment. Clinical case: The clinical case of a RICH with incipient signs of heart failure is presented, it required an interdisciplinary approach with dermatologists, neonatologists, obstetricians and specialists in diagnostic imaging, to define diagnosis, conduct and follow-up. Postnatal follow-up was performed until complete and spontaneous involution, leaving almost no sequelae, despite the large size of the tumor. Conclusion: It is important to take into consideration the diagnosis of RICH, among intrauterine high-flow vascular tumors, so as not to perform unnecessary interventions.
publisher Universidad Nacional Córdoba. Facultad de Ciencias Médicas. Secretaria de Ciencia y Tecnología
publishDate 2026
url https://revistas.unc.edu.ar/index.php/med/article/view/44679
work_keys_str_mv AT santarelliagustina rapidlyinvolutingcongenitalhemangiomadiagnosedprenatallywithheartfailureandposnatalfollowup
AT gimenezmariacandelaria rapidlyinvolutingcongenitalhemangiomadiagnosedprenatallywithheartfailureandposnatalfollowup
AT saldunamariadolores rapidlyinvolutingcongenitalhemangiomadiagnosedprenatallywithheartfailureandposnatalfollowup
AT valenteenrique rapidlyinvolutingcongenitalhemangiomadiagnosedprenatallywithheartfailureandposnatalfollowup
AT santarelliagustina hemangiomacongenitorapidamenteinvolutivodiagnosticadoprenatalmenteconinsuficienciacardiacayseguimientopostnatal
AT gimenezmariacandelaria hemangiomacongenitorapidamenteinvolutivodiagnosticadoprenatalmenteconinsuficienciacardiacayseguimientopostnatal
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first_indexed 2026-03-27T05:14:33Z
last_indexed 2026-03-27T05:14:33Z
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spelling I10-R327-article-446792026-03-13T16:59:06Z Rapidly involuting congenital hemangioma, diagnosed prenatally with heart failure and posnatal follow up. Hemangioma congénito rápidamente involutivo, diagnosticado prenatalmente con insuficiencia cardíaca y seguimiento postnatal Hemangioma congênito de rápida involução, diagnosticado no pré-natal com insuficiência cardíaca e acompanhamento pós-natal Santarelli, Agustina Gimenez, María Candelaria Salduna, María Dolores Valente, Enrique tumor hemangiomas heart failure tumor hemangioma insuficiencia cardiaca Insuficiência Cardíaca tumor hemangioma Objectives: Describe the clinical case of a RICH that was diagnosed in uterus, normally in obstetric ultrasounds they are often confused with arteriovenous malformations and other congenital tumors. The differential diagnosis of these entities is important, since they have a different evolution, prognosis and treatment. Clinical case: The clinical case of a RICH with incipient signs of heart failure is presented, it required an interdisciplinary approach with dermatologists, neonatologists, obstetricians and specialists in diagnostic imaging, to define diagnosis, conduct and follow-up. Postnatal follow-up was performed until complete and spontaneous involution, leaving almost no sequelae, despite the large size of the tumor. Conclusion: It is important to take into consideration the diagnosis of RICH, among intrauterine high-flow vascular tumors, so as not to perform unnecessary interventions. Objetivos: Describir el caso clínico de un RICH que fue diagnosticado intraútero, normalmente en las ecografías obstétricas suelen ser confundidos con malformaciones arteriovenosas y otros tumores congénitos. El diagnóstico diferencial de estas entidades es importante, ya que estos tienen una evolución, pronóstico y tratamiento diferentes. Caso clínico: Se presenta el caso clínico de un RICH con signos incipientes de insuficiencia cardíaca que requirió un abordaje interdisciplinario con dermatólogos, neonatólogos, obstetras y especialistas en diagnósticos por imágenes, para definir diagnóstico, conducta y seguimiento. Se realizó seguimiento posnatal hasta su  involución completa y espontánea, sin dejar casi secuelas, a pesar del gran tamaño del tumor.                                Conclusión: Es importante tener en consideración el diagnóstico de RICH, entre las  tumoraciones vasculares de alto flujo intrauterinas, para no realizar intervenciones innecesarias. Objetivos: Descrever o caso clínico de uma RICH que foi diagnosticada ainda no útero, normalmente em ultrassonografias obstétricas são frequentemente confundidas com malformações arteriovenosas e outros tumores congênitos. O diagnóstico diferencial destas entidades é importante, uma vez que apresentam evolução, prognóstico e tratamento diferentes. Caso clínico: É apresentado o caso clínico de um RICH com sinais incipientes de insuficiência cardíaca que exigiu uma abordagem interdisciplinar com dermatologistas, neonatologistas, obstetras e especialistas em diagnóstico por imagem, para definição do diagnóstico, conduta e acompanhamento. O acompanhamento pós-natal foi realizado até a involução completa e espontânea, quase sem deixar sequelas, apesar do grande tamanho do tumor. Conclusão: É importante levar em consideração o diagnóstico de RICH, dentre os tumores vasculares intrauterinos de alto fluxo, para não realizar intervenções desnecessárias. Universidad Nacional Córdoba. Facultad de Ciencias Médicas. Secretaria de Ciencia y Tecnología 2026-03-13 info:eu-repo/semantics/article info:eu-repo/semantics/publishedVersion application/pdf https://revistas.unc.edu.ar/index.php/med/article/view/44679 10.31053/1853.0605.v83.n1.44679 Revista de la Facultad de Ciencias Médicas de Córdoba.; Vol. 83 No. 1 (2026): Avance de publicación; e44679 Revista de la Facultad de Ciencias Médicas de Córdoba; Vol. 83 Núm. 1 (2026): Avance de publicación; e44679 Revista da Faculdade de Ciências Médicas de Córdoba; v. 83 n. 1 (2026): Avance de publicación; e44679 1853-0605 0014-6722 10.31053/1853.0605.v83.n1 spa https://revistas.unc.edu.ar/index.php/med/article/view/44679/52569 Derechos de autor 2026 Universidad Nacional de Córdoba https://creativecommons.org/licenses/by-nc/4.0

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