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Recurring hematuria revealing absence of infrarenal segment of the inferior vena cava

Abnormal development of the inferior vena cava is a relatively rare condition. We report the case of a 47-year-old woman presenting with an absent infrarenal segment of the inferior vena cava revealed by recurring episodes of gross hematuria. This entity probably resulted from perinatal acquired thr...

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Detalles Bibliográficos
Autores principales: Louagé, Fabian, Moradi, Massoud, Vanrossomme, Axel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9440369/
https://www.ncbi.nlm.nih.gov/pubmed/36065243
http://dx.doi.org/10.1016/j.radcr.2022.07.112
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author Louagé, Fabian
Moradi, Massoud
Vanrossomme, Axel
author_facet Louagé, Fabian
Moradi, Massoud
Vanrossomme, Axel
author_sort Louagé, Fabian
collection PubMed
description Abnormal development of the inferior vena cava is a relatively rare condition. We report the case of a 47-year-old woman presenting with an absent infrarenal segment of the inferior vena cava revealed by recurring episodes of gross hematuria. This entity probably resulted from perinatal acquired thrombosis rather than from a congenital anomaly and is associated with compensatory dilation of collateral venous pathways. This extremely rare hemorrhagic presentation is presumably caused by rupture of small dilated renal or vesical veins. Ignorance of this atypical presentation can lead to erroneous or delayed diagnoses.
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spelling pubmed-94403692022-09-04 Recurring hematuria revealing absence of infrarenal segment of the inferior vena cava Louagé, Fabian Moradi, Massoud Vanrossomme, Axel Radiol Case Rep Case Report Abnormal development of the inferior vena cava is a relatively rare condition. We report the case of a 47-year-old woman presenting with an absent infrarenal segment of the inferior vena cava revealed by recurring episodes of gross hematuria. This entity probably resulted from perinatal acquired thrombosis rather than from a congenital anomaly and is associated with compensatory dilation of collateral venous pathways. This extremely rare hemorrhagic presentation is presumably caused by rupture of small dilated renal or vesical veins. Ignorance of this atypical presentation can lead to erroneous or delayed diagnoses. Elsevier 2022-08-27 /pmc/articles/PMC9440369/ /pubmed/36065243 http://dx.doi.org/10.1016/j.radcr.2022.07.112 Text en © 2022 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
Louagé, Fabian
Moradi, Massoud
Vanrossomme, Axel
Recurring hematuria revealing absence of infrarenal segment of the inferior vena cava
title Recurring hematuria revealing absence of infrarenal segment of the inferior vena cava
title_full Recurring hematuria revealing absence of infrarenal segment of the inferior vena cava
title_fullStr Recurring hematuria revealing absence of infrarenal segment of the inferior vena cava
title_full_unstemmed Recurring hematuria revealing absence of infrarenal segment of the inferior vena cava
title_short Recurring hematuria revealing absence of infrarenal segment of the inferior vena cava
title_sort recurring hematuria revealing absence of infrarenal segment of the inferior vena cava
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9440369/
https://www.ncbi.nlm.nih.gov/pubmed/36065243
http://dx.doi.org/10.1016/j.radcr.2022.07.112
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