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Extensive solitary lymphatic malformation of the liver in a child: a case report and literature review

Intrabdominal lymphatic malformations are rare benign congenital vascular anomalies that account for less than 5% of benign masses in childhood, with an extremely variable clinical presentation. For this reason, although their radiological appearance is usually typical, diagnosis can be challenging...

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Autores principales: Parmeggiani, Anna, Baldazzi, Michelangelo, Carfagnini, Filomena, Vivacqua, Donatella, Golfieri, Rita, Lovato, Luigi, Greco, Laura
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8666449/
https://www.ncbi.nlm.nih.gov/pubmed/34917222
http://dx.doi.org/10.1016/j.radcr.2021.11.022
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author Parmeggiani, Anna
Baldazzi, Michelangelo
Carfagnini, Filomena
Vivacqua, Donatella
Golfieri, Rita
Lovato, Luigi
Greco, Laura
author_facet Parmeggiani, Anna
Baldazzi, Michelangelo
Carfagnini, Filomena
Vivacqua, Donatella
Golfieri, Rita
Lovato, Luigi
Greco, Laura
author_sort Parmeggiani, Anna
collection PubMed
description Intrabdominal lymphatic malformations are rare benign congenital vascular anomalies that account for less than 5% of benign masses in childhood, with an extremely variable clinical presentation. For this reason, although their radiological appearance is usually typical, diagnosis can be challenging and not always immediate. This report describes a unique case of extensive solitary hepatic lymphatic malformation in a 10-year-old boy with both extra- and intraparenchymal development with no associated symptoms. A literature review of reported cases of solitary hepatic lymphatic malformation is also included.
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spelling pubmed-86664492021-12-15 Extensive solitary lymphatic malformation of the liver in a child: a case report and literature review Parmeggiani, Anna Baldazzi, Michelangelo Carfagnini, Filomena Vivacqua, Donatella Golfieri, Rita Lovato, Luigi Greco, Laura Radiol Case Rep Case Report Intrabdominal lymphatic malformations are rare benign congenital vascular anomalies that account for less than 5% of benign masses in childhood, with an extremely variable clinical presentation. For this reason, although their radiological appearance is usually typical, diagnosis can be challenging and not always immediate. This report describes a unique case of extensive solitary hepatic lymphatic malformation in a 10-year-old boy with both extra- and intraparenchymal development with no associated symptoms. A literature review of reported cases of solitary hepatic lymphatic malformation is also included. Elsevier 2021-12-09 /pmc/articles/PMC8666449/ /pubmed/34917222 http://dx.doi.org/10.1016/j.radcr.2021.11.022 Text en © 2021 The Authors. Published by Elsevier Inc. on behalf of University of Washington. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Case Report
Parmeggiani, Anna
Baldazzi, Michelangelo
Carfagnini, Filomena
Vivacqua, Donatella
Golfieri, Rita
Lovato, Luigi
Greco, Laura
Extensive solitary lymphatic malformation of the liver in a child: a case report and literature review
title Extensive solitary lymphatic malformation of the liver in a child: a case report and literature review
title_full Extensive solitary lymphatic malformation of the liver in a child: a case report and literature review
title_fullStr Extensive solitary lymphatic malformation of the liver in a child: a case report and literature review
title_full_unstemmed Extensive solitary lymphatic malformation of the liver in a child: a case report and literature review
title_short Extensive solitary lymphatic malformation of the liver in a child: a case report and literature review
title_sort extensive solitary lymphatic malformation of the liver in a child: a case report and literature review
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8666449/
https://www.ncbi.nlm.nih.gov/pubmed/34917222
http://dx.doi.org/10.1016/j.radcr.2021.11.022
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