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Retroperitoneal lymphatic malformations: A case report

Retroperitoneal lymphatic malformation is a rare benign vascular malformation, of various locations, which can reveal itself at any age in its abdominal localizations. The retroperitoneal localization of this malformation is extremely rare. The clinical symptomatology is polymorphic depending on the...

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Autores principales: Zebbakh, Hajar, Imrani, Kaoutar, Lemrabet, Abir, Aaboudech, Taha Yassine, Bernoussi, Zakia, MoatassimBillah, Nabil, Nassar, Ittimade
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10315919/
https://www.ncbi.nlm.nih.gov/pubmed/37404219
http://dx.doi.org/10.1016/j.radcr.2023.05.078
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author Zebbakh, Hajar
Imrani, Kaoutar
Lemrabet, Abir
Aaboudech, Taha Yassine
Bernoussi, Zakia
MoatassimBillah, Nabil
Nassar, Ittimade
author_facet Zebbakh, Hajar
Imrani, Kaoutar
Lemrabet, Abir
Aaboudech, Taha Yassine
Bernoussi, Zakia
MoatassimBillah, Nabil
Nassar, Ittimade
author_sort Zebbakh, Hajar
collection PubMed
description Retroperitoneal lymphatic malformation is a rare benign vascular malformation, of various locations, which can reveal itself at any age in its abdominal localizations. The retroperitoneal localization of this malformation is extremely rare. The clinical symptomatology is polymorphic depending on the lesion volume and the presence or absence of complications. The diagnosis is evoked by the liquid character of the retroperitoneal mass on ultrasound, CT scan and abdomino-pelvic MRI, brought during surgery and confirmed by the histological study of the surgical specimen. The treatment of choice is complete surgical removal of the mass.
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spelling pubmed-103159192023-07-04 Retroperitoneal lymphatic malformations: A case report Zebbakh, Hajar Imrani, Kaoutar Lemrabet, Abir Aaboudech, Taha Yassine Bernoussi, Zakia MoatassimBillah, Nabil Nassar, Ittimade Radiol Case Rep Case Report Retroperitoneal lymphatic malformation is a rare benign vascular malformation, of various locations, which can reveal itself at any age in its abdominal localizations. The retroperitoneal localization of this malformation is extremely rare. The clinical symptomatology is polymorphic depending on the lesion volume and the presence or absence of complications. The diagnosis is evoked by the liquid character of the retroperitoneal mass on ultrasound, CT scan and abdomino-pelvic MRI, brought during surgery and confirmed by the histological study of the surgical specimen. The treatment of choice is complete surgical removal of the mass. Elsevier 2023-06-27 /pmc/articles/PMC10315919/ /pubmed/37404219 http://dx.doi.org/10.1016/j.radcr.2023.05.078 Text en © 2023 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
Zebbakh, Hajar
Imrani, Kaoutar
Lemrabet, Abir
Aaboudech, Taha Yassine
Bernoussi, Zakia
MoatassimBillah, Nabil
Nassar, Ittimade
Retroperitoneal lymphatic malformations: A case report
title Retroperitoneal lymphatic malformations: A case report
title_full Retroperitoneal lymphatic malformations: A case report
title_fullStr Retroperitoneal lymphatic malformations: A case report
title_full_unstemmed Retroperitoneal lymphatic malformations: A case report
title_short Retroperitoneal lymphatic malformations: A case report
title_sort retroperitoneal lymphatic malformations: a case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10315919/
https://www.ncbi.nlm.nih.gov/pubmed/37404219
http://dx.doi.org/10.1016/j.radcr.2023.05.078
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