Intravascular leiomyomatosis with cardiac extension, a case report

Abstract Background Intravascular leiomyomatosis (IVL) is a histologically benign smooth muscle tumor arising from the uterus that can spread through the pelvic veins and, on rare occasions, extend as far as the heart via the inferior vena cava. Despite its benign characteristics, it can behave like...

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Main Authors: Juan Garcés Garcés, Fernando Terán Camacho, Gerardo Dávalos Dávalos, Sofía Zárate León, Ligia Redrobán Armendáriz, Vladimir Ullauri Solórzano, Gabriel A. Molina, Santiago Endara Aguirre
Format: Article
Language:English
Published: BMC 2023-09-01
Series:Journal of Cardiothoracic Surgery
Subjects:
Online Access:https://doi.org/10.1186/s13019-023-02344-9
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author Juan Garcés Garcés
Fernando Terán Camacho
Gerardo Dávalos Dávalos
Sofía Zárate León
Ligia Redrobán Armendáriz
Vladimir Ullauri Solórzano
Gabriel A. Molina
Santiago Endara Aguirre
author_facet Juan Garcés Garcés
Fernando Terán Camacho
Gerardo Dávalos Dávalos
Sofía Zárate León
Ligia Redrobán Armendáriz
Vladimir Ullauri Solórzano
Gabriel A. Molina
Santiago Endara Aguirre
author_sort Juan Garcés Garcés
collection DOAJ
description Abstract Background Intravascular leiomyomatosis (IVL) is a histologically benign smooth muscle tumor arising from the uterus that can spread through the pelvic veins and, on rare occasions, extend as far as the heart via the inferior vena cava. Despite its benign characteristics, it can behave like a malignant tumor leading to significant morbidity and even mortality if left untreated. Case presentation The patient is a 42-year-old woman with a past medical history of uterine leiomyomas. She presented with heavy bleeding and frequent spotting; therefore, she went to her gynecologist. After further evaluation, a mass within the uterus that expanded into the pelvic veins, inferior vena cava, and right atrium was discovered. After the complete removal of the mass, the patient underwent full recovery. IVL with cardiac extension was the final diagnosis. Conclusion Although IVL is rare, it must be considered in women who underwent previous hysterectomies or myomectomies and present with symptoms of right heart failure. The ideal therapy will need the aid of a multidisciplinary team and will depend on the patient’s symptoms, previous operative history, the tumor’s extension, and resectability.
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spelling doaj.art-d03adc52ac884ae1871b78a5c42593562023-11-26T14:12:12ZengBMCJournal of Cardiothoracic Surgery1749-80902023-09-011811510.1186/s13019-023-02344-9Intravascular leiomyomatosis with cardiac extension, a case reportJuan Garcés Garcés0Fernando Terán Camacho1Gerardo Dávalos Dávalos2Sofía Zárate León3Ligia Redrobán Armendáriz4Vladimir Ullauri Solórzano5Gabriel A. Molina6Santiago Endara Aguirre7Radiology Service, Internal Medicine Department, Hospital MetropolitanoOncological Surgery, Surgery Department, Hospital MetropolitanoCardiothoracic Surgery, Surgery Department, Hospital MetropolitanoGeneral Surgery, Surgery Department, Hospital MetropolitanoPathology Service, Internal Medicine Department, Hospital MetropolitanoCardiology Service, Internal Medicine Department, Hospital MetropolitanoGeneral Surgery, Surgery Department, Hospital Metropolitano & USFQCardiothoracic Surgery, Surgery Department, Hospital MetropolitanoAbstract Background Intravascular leiomyomatosis (IVL) is a histologically benign smooth muscle tumor arising from the uterus that can spread through the pelvic veins and, on rare occasions, extend as far as the heart via the inferior vena cava. Despite its benign characteristics, it can behave like a malignant tumor leading to significant morbidity and even mortality if left untreated. Case presentation The patient is a 42-year-old woman with a past medical history of uterine leiomyomas. She presented with heavy bleeding and frequent spotting; therefore, she went to her gynecologist. After further evaluation, a mass within the uterus that expanded into the pelvic veins, inferior vena cava, and right atrium was discovered. After the complete removal of the mass, the patient underwent full recovery. IVL with cardiac extension was the final diagnosis. Conclusion Although IVL is rare, it must be considered in women who underwent previous hysterectomies or myomectomies and present with symptoms of right heart failure. The ideal therapy will need the aid of a multidisciplinary team and will depend on the patient’s symptoms, previous operative history, the tumor’s extension, and resectability.https://doi.org/10.1186/s13019-023-02344-9Intravascular leiomyomatosis (IVL)Heart TumorVascular growth
spellingShingle Juan Garcés Garcés
Fernando Terán Camacho
Gerardo Dávalos Dávalos
Sofía Zárate León
Ligia Redrobán Armendáriz
Vladimir Ullauri Solórzano
Gabriel A. Molina
Santiago Endara Aguirre
Intravascular leiomyomatosis with cardiac extension, a case report
Journal of Cardiothoracic Surgery
Intravascular leiomyomatosis (IVL)
Heart Tumor
Vascular growth
title Intravascular leiomyomatosis with cardiac extension, a case report
title_full Intravascular leiomyomatosis with cardiac extension, a case report
title_fullStr Intravascular leiomyomatosis with cardiac extension, a case report
title_full_unstemmed Intravascular leiomyomatosis with cardiac extension, a case report
title_short Intravascular leiomyomatosis with cardiac extension, a case report
title_sort intravascular leiomyomatosis with cardiac extension a case report
topic Intravascular leiomyomatosis (IVL)
Heart Tumor
Vascular growth
url https://doi.org/10.1186/s13019-023-02344-9
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