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A rare case of left inferior vena cava presenting with May-Thurner syndrome
BACKGROUND: May–Thurner anomaly is characterized as external venous compression by the arterial framework against hard bony structures. This chronic anatomical lesion infrequently leads to deep vein thrombosis in the lower extremity, and it may lead to leg swelling as a long-term post-thrombotic com...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer International Publishing
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9249960/ https://www.ncbi.nlm.nih.gov/pubmed/35776262 http://dx.doi.org/10.1186/s42155-022-00305-2 |
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author | Moosavi, Jamal Sadeghipour, Parham Mohebbi, Bahram Rezaei-Kalantari, Kiara Khalilipur, Ehsan |
author_facet | Moosavi, Jamal Sadeghipour, Parham Mohebbi, Bahram Rezaei-Kalantari, Kiara Khalilipur, Ehsan |
author_sort | Moosavi, Jamal |
collection | PubMed |
description | BACKGROUND: May–Thurner anomaly is characterized as external venous compression by the arterial framework against hard bony structures. This chronic anatomical lesion infrequently leads to deep vein thrombosis in the lower extremity, and it may lead to leg swelling as a long-term post-thrombotic complication. Left iliac vein compression may not be as uncommon as was previously thought, and it typically occurs in women more than men. Congenital anomalies of venous tree are not rare; they exist in 8.7% of the general population. CASE-PRESENTATION: We herein present the first case of right-sided May Thurner Syndrome in a patient with IVC anomalies. In our patient, both common iliac veins formed the left-sided IVC, which extended to the hemiazygos vein and the superior vena cava. Additionally, there was a right-sided suprarenal IVC, which extended to the right atrium. CONCLUSION: Understanding the proper anatomy in May-Thurner syndrome helps in better decision making for management of disease pathophysiology. |
format | Online Article Text |
id | pubmed-9249960 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Springer International Publishing |
record_format | MEDLINE/PubMed |
spelling | pubmed-92499602022-07-03 A rare case of left inferior vena cava presenting with May-Thurner syndrome Moosavi, Jamal Sadeghipour, Parham Mohebbi, Bahram Rezaei-Kalantari, Kiara Khalilipur, Ehsan CVIR Endovasc Case Report BACKGROUND: May–Thurner anomaly is characterized as external venous compression by the arterial framework against hard bony structures. This chronic anatomical lesion infrequently leads to deep vein thrombosis in the lower extremity, and it may lead to leg swelling as a long-term post-thrombotic complication. Left iliac vein compression may not be as uncommon as was previously thought, and it typically occurs in women more than men. Congenital anomalies of venous tree are not rare; they exist in 8.7% of the general population. CASE-PRESENTATION: We herein present the first case of right-sided May Thurner Syndrome in a patient with IVC anomalies. In our patient, both common iliac veins formed the left-sided IVC, which extended to the hemiazygos vein and the superior vena cava. Additionally, there was a right-sided suprarenal IVC, which extended to the right atrium. CONCLUSION: Understanding the proper anatomy in May-Thurner syndrome helps in better decision making for management of disease pathophysiology. Springer International Publishing 2022-07-01 /pmc/articles/PMC9249960/ /pubmed/35776262 http://dx.doi.org/10.1186/s42155-022-00305-2 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Case Report Moosavi, Jamal Sadeghipour, Parham Mohebbi, Bahram Rezaei-Kalantari, Kiara Khalilipur, Ehsan A rare case of left inferior vena cava presenting with May-Thurner syndrome |
title | A rare case of left inferior vena cava presenting with May-Thurner syndrome |
title_full | A rare case of left inferior vena cava presenting with May-Thurner syndrome |
title_fullStr | A rare case of left inferior vena cava presenting with May-Thurner syndrome |
title_full_unstemmed | A rare case of left inferior vena cava presenting with May-Thurner syndrome |
title_short | A rare case of left inferior vena cava presenting with May-Thurner syndrome |
title_sort | rare case of left inferior vena cava presenting with may-thurner syndrome |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9249960/ https://www.ncbi.nlm.nih.gov/pubmed/35776262 http://dx.doi.org/10.1186/s42155-022-00305-2 |
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