Cargando…

Intracardiac Leiomyomatosis Arising from a Uterine Leiomyoma – A Rare Case Requiring a Multidisciplinary Laparotomy–Thoracotomy Approach

A 37-year-old lady, when being evaluated in gynecology for pain in the abdomen, was found to have a pelvic mass suspicious of ovarian cancer with markers negative. There was an ovarian vein thrombosis extending to the right atrium in the contrast-enhanced computed tomography scan. A fluorodeoxygluco...

Descripción completa

Detalles Bibliográficos
Autores principales: Murali, T. V., Thomas, Reshma Sara, Pilllai, Manjusha Narayana, Gopal, Anitha
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer - Medknow 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10482015/
https://www.ncbi.nlm.nih.gov/pubmed/37680381
http://dx.doi.org/10.4103/jmh.jmh_47_23
_version_ 1785102099316473856
author Murali, T. V.
Thomas, Reshma Sara
Pilllai, Manjusha Narayana
Gopal, Anitha
author_facet Murali, T. V.
Thomas, Reshma Sara
Pilllai, Manjusha Narayana
Gopal, Anitha
author_sort Murali, T. V.
collection PubMed
description A 37-year-old lady, when being evaluated in gynecology for pain in the abdomen, was found to have a pelvic mass suspicious of ovarian cancer with markers negative. There was an ovarian vein thrombosis extending to the right atrium in the contrast-enhanced computed tomography scan. A fluorodeoxyglucose positron emission tomography-computed tomography ruled out any other lesions. The patient underwent surgery under general anesthesia with transesophageal echocardiography to monitor the atrial thrombus. Intraoperatively, a retroperitoneal mass is seen arising from the right adnexal region of the uterus extending to the lumbar area. After the hysterectomy, bilateral salpingo-oophorectomy, tumor resection, and baring and looping of the retroperitoneal vessels, a sternotomy was done, and she was put on cardiopulmonary bypass. The tumor thrombus had two limbs both arising from the mass, one through the ovarian and the second through the iliac veins and joining together inside the inferior vena cava (IVC). With the excision of the ovarian vein at its junction, atrial incision, and incisions over the iliac veins and IVC, the thrombus was removed completely in a single sitting. Final histopathology revealed intravenous leiomyomatosis and no malignancy. We report this case as a rare disease, with both ovarian and iliac thrombus being a further rarity and a multidepartment joint effort with a successful outcome.
format Online
Article
Text
id pubmed-10482015
institution National Center for Biotechnology Information
language English
publishDate 2023
publisher Wolters Kluwer - Medknow
record_format MEDLINE/PubMed
spelling pubmed-104820152023-09-07 Intracardiac Leiomyomatosis Arising from a Uterine Leiomyoma – A Rare Case Requiring a Multidisciplinary Laparotomy–Thoracotomy Approach Murali, T. V. Thomas, Reshma Sara Pilllai, Manjusha Narayana Gopal, Anitha J Midlife Health Case Report A 37-year-old lady, when being evaluated in gynecology for pain in the abdomen, was found to have a pelvic mass suspicious of ovarian cancer with markers negative. There was an ovarian vein thrombosis extending to the right atrium in the contrast-enhanced computed tomography scan. A fluorodeoxyglucose positron emission tomography-computed tomography ruled out any other lesions. The patient underwent surgery under general anesthesia with transesophageal echocardiography to monitor the atrial thrombus. Intraoperatively, a retroperitoneal mass is seen arising from the right adnexal region of the uterus extending to the lumbar area. After the hysterectomy, bilateral salpingo-oophorectomy, tumor resection, and baring and looping of the retroperitoneal vessels, a sternotomy was done, and she was put on cardiopulmonary bypass. The tumor thrombus had two limbs both arising from the mass, one through the ovarian and the second through the iliac veins and joining together inside the inferior vena cava (IVC). With the excision of the ovarian vein at its junction, atrial incision, and incisions over the iliac veins and IVC, the thrombus was removed completely in a single sitting. Final histopathology revealed intravenous leiomyomatosis and no malignancy. We report this case as a rare disease, with both ovarian and iliac thrombus being a further rarity and a multidepartment joint effort with a successful outcome. Wolters Kluwer - Medknow 2023 2023-07-07 /pmc/articles/PMC10482015/ /pubmed/37680381 http://dx.doi.org/10.4103/jmh.jmh_47_23 Text en Copyright: © 2023 Journal of Mid-life Health 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
Murali, T. V.
Thomas, Reshma Sara
Pilllai, Manjusha Narayana
Gopal, Anitha
Intracardiac Leiomyomatosis Arising from a Uterine Leiomyoma – A Rare Case Requiring a Multidisciplinary Laparotomy–Thoracotomy Approach
title Intracardiac Leiomyomatosis Arising from a Uterine Leiomyoma – A Rare Case Requiring a Multidisciplinary Laparotomy–Thoracotomy Approach
title_full Intracardiac Leiomyomatosis Arising from a Uterine Leiomyoma – A Rare Case Requiring a Multidisciplinary Laparotomy–Thoracotomy Approach
title_fullStr Intracardiac Leiomyomatosis Arising from a Uterine Leiomyoma – A Rare Case Requiring a Multidisciplinary Laparotomy–Thoracotomy Approach
title_full_unstemmed Intracardiac Leiomyomatosis Arising from a Uterine Leiomyoma – A Rare Case Requiring a Multidisciplinary Laparotomy–Thoracotomy Approach
title_short Intracardiac Leiomyomatosis Arising from a Uterine Leiomyoma – A Rare Case Requiring a Multidisciplinary Laparotomy–Thoracotomy Approach
title_sort intracardiac leiomyomatosis arising from a uterine leiomyoma – a rare case requiring a multidisciplinary laparotomy–thoracotomy approach
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10482015/
https://www.ncbi.nlm.nih.gov/pubmed/37680381
http://dx.doi.org/10.4103/jmh.jmh_47_23
work_keys_str_mv AT muralitv intracardiacleiomyomatosisarisingfromauterineleiomyomaararecaserequiringamultidisciplinarylaparotomythoracotomyapproach
AT thomasreshmasara intracardiacleiomyomatosisarisingfromauterineleiomyomaararecaserequiringamultidisciplinarylaparotomythoracotomyapproach
AT pilllaimanjushanarayana intracardiacleiomyomatosisarisingfromauterineleiomyomaararecaserequiringamultidisciplinarylaparotomythoracotomyapproach
AT gopalanitha intracardiacleiomyomatosisarisingfromauterineleiomyomaararecaserequiringamultidisciplinarylaparotomythoracotomyapproach