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Combination between Dunbar Syndrome and May–Thurner Syndrome: A Rare Case Report

Dunbar syndrome (DS) and May–Thurner syndrome (MTS) are part of a group of rare vascular disorders known as “vascular compression syndromes.” Dunbar’s syndrome is caused by the median arcuate ligament of diaphragm, which, due to an abnormal course, causes celiac artery compression. MTS is caused by...

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Autores principales: Farina, Renato, Galioto, Federica, Castiglione, Davide, Basile, Antonio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer - Medknow 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10668899/
https://www.ncbi.nlm.nih.gov/pubmed/38024998
http://dx.doi.org/10.4103/jmu.jmu_27_22
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author Farina, Renato
Galioto, Federica
Castiglione, Davide
Basile, Antonio
author_facet Farina, Renato
Galioto, Federica
Castiglione, Davide
Basile, Antonio
author_sort Farina, Renato
collection PubMed
description Dunbar syndrome (DS) and May–Thurner syndrome (MTS) are part of a group of rare vascular disorders known as “vascular compression syndromes.” Dunbar’s syndrome is caused by the median arcuate ligament of diaphragm, which, due to an abnormal course, causes celiac artery compression. MTS is caused by the left common iliac vein compression pushed against the spine by the right common iliac artery causing progressive flow congestion and leading to thrombosis. Ultrasound is the first-level examination for the diagnosis of these rare pathologies and allows to recognize vascular compressions and to obtain an estimate of stenosis degree. We describe a very rare case of DS and MTS combination in a young man with postprandial pain and left lower limb thrombosis.
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spelling pubmed-106688992022-10-07 Combination between Dunbar Syndrome and May–Thurner Syndrome: A Rare Case Report Farina, Renato Galioto, Federica Castiglione, Davide Basile, Antonio J Med Ultrasound Case Report Dunbar syndrome (DS) and May–Thurner syndrome (MTS) are part of a group of rare vascular disorders known as “vascular compression syndromes.” Dunbar’s syndrome is caused by the median arcuate ligament of diaphragm, which, due to an abnormal course, causes celiac artery compression. MTS is caused by the left common iliac vein compression pushed against the spine by the right common iliac artery causing progressive flow congestion and leading to thrombosis. Ultrasound is the first-level examination for the diagnosis of these rare pathologies and allows to recognize vascular compressions and to obtain an estimate of stenosis degree. We describe a very rare case of DS and MTS combination in a young man with postprandial pain and left lower limb thrombosis. Wolters Kluwer - Medknow 2022-10-07 /pmc/articles/PMC10668899/ /pubmed/38024998 http://dx.doi.org/10.4103/jmu.jmu_27_22 Text en Copyright: © 2022 Journal of Medical Ultrasound https://creativecommons.org/licenses/by-nc-sa/4.0/This is an open access journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms.
spellingShingle Case Report
Farina, Renato
Galioto, Federica
Castiglione, Davide
Basile, Antonio
Combination between Dunbar Syndrome and May–Thurner Syndrome: A Rare Case Report
title Combination between Dunbar Syndrome and May–Thurner Syndrome: A Rare Case Report
title_full Combination between Dunbar Syndrome and May–Thurner Syndrome: A Rare Case Report
title_fullStr Combination between Dunbar Syndrome and May–Thurner Syndrome: A Rare Case Report
title_full_unstemmed Combination between Dunbar Syndrome and May–Thurner Syndrome: A Rare Case Report
title_short Combination between Dunbar Syndrome and May–Thurner Syndrome: A Rare Case Report
title_sort combination between dunbar syndrome and may–thurner syndrome: a rare case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10668899/
https://www.ncbi.nlm.nih.gov/pubmed/38024998
http://dx.doi.org/10.4103/jmu.jmu_27_22
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