Congenital liver hemangioma revealed by cholestasis syndrome: report of a rare case

Our paper reports a case of hepatic angioma revealed by neonatal cholestasis, thing that has never been reported in the literature to our knowledge. A newborn boy of 25 days of life had cholestatic jaundice since his fifth day of life. During its health assessment, the angioscan detected the presenc...

Descripción completa

Detalles Bibliográficos
Autores principales: Khairoun, Chaimae, Barkat, Amina
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The African Field Epidemiology Network 2020
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7467625/
https://www.ncbi.nlm.nih.gov/pubmed/32952836
http://dx.doi.org/10.11604/pamj.2020.36.192.21411
_version_ 1783578053616599040
author Khairoun, Chaimae
Barkat, Amina
author_facet Khairoun, Chaimae
Barkat, Amina
author_sort Khairoun, Chaimae
collection PubMed
description Our paper reports a case of hepatic angioma revealed by neonatal cholestasis, thing that has never been reported in the literature to our knowledge. A newborn boy of 25 days of life had cholestatic jaundice since his fifth day of life. During its health assessment, the angioscan detected the presence of multiple hepatic agiomas. The rest of the etiological report returned without any anomaly. Beta-blockers were started with a very good clinical and ultrasonographic evolution after 12 months of treatment.
format Online
Article
Text
id pubmed-7467625
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher The African Field Epidemiology Network
record_format MEDLINE/PubMed
spelling pubmed-74676252020-09-17 Congenital liver hemangioma revealed by cholestasis syndrome: report of a rare case Khairoun, Chaimae Barkat, Amina Pan Afr Med J Case Report Our paper reports a case of hepatic angioma revealed by neonatal cholestasis, thing that has never been reported in the literature to our knowledge. A newborn boy of 25 days of life had cholestatic jaundice since his fifth day of life. During its health assessment, the angioscan detected the presence of multiple hepatic agiomas. The rest of the etiological report returned without any anomaly. Beta-blockers were started with a very good clinical and ultrasonographic evolution after 12 months of treatment. The African Field Epidemiology Network 2020-07-17 /pmc/articles/PMC7467625/ /pubmed/32952836 http://dx.doi.org/10.11604/pamj.2020.36.192.21411 Text en Copyright: Chaimae Khairoun et al. https://creativecommons.org/licenses/by/4.0 The Pan African Medical Journal (ISSN: 1937-8688). This is an Open Access article distributed under the terms of the Creative Commons Attribution International 4.0 License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Khairoun, Chaimae
Barkat, Amina
Congenital liver hemangioma revealed by cholestasis syndrome: report of a rare case
title Congenital liver hemangioma revealed by cholestasis syndrome: report of a rare case
title_full Congenital liver hemangioma revealed by cholestasis syndrome: report of a rare case
title_fullStr Congenital liver hemangioma revealed by cholestasis syndrome: report of a rare case
title_full_unstemmed Congenital liver hemangioma revealed by cholestasis syndrome: report of a rare case
title_short Congenital liver hemangioma revealed by cholestasis syndrome: report of a rare case
title_sort congenital liver hemangioma revealed by cholestasis syndrome: report of a rare case
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7467625/
https://www.ncbi.nlm.nih.gov/pubmed/32952836
http://dx.doi.org/10.11604/pamj.2020.36.192.21411
work_keys_str_mv AT khairounchaimae congenitalliverhemangiomarevealedbycholestasissyndromereportofararecase
AT barkatamina congenitalliverhemangiomarevealedbycholestasissyndromereportofararecase

Ejemplares similares