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A case of a large leiomyomatous uterus with multiple arteriovenous malformations and subsequent high cardiac output state with severe four chamber cardiac enlargement

Uterine arteriovenous malformations (AVMs) are rare and potentially life-threatening. They can be congenital or acquired. Uterine artery embolization or hysterectomy are considered mainstays of management. AVMs can be associated with leiomyomas, and patients may require both procedures. We present a...

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Detalles Bibliográficos
Autores principales: Vega, Beatriz, Stockland, Andrew H., Bramblet, Rachel M., Anderson, Alexandra L., Mankad, Rekha, Khan, Zaraq, Mustafa, Mohamed, Steyermark, Joan M., Fields, Amanda R., Berntson, Novette J., Kenneth Schoolmeester, J., Colglazier, Jill J., Bakkum-Gamez, Jamie N.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8651894/
https://www.ncbi.nlm.nih.gov/pubmed/34926776
http://dx.doi.org/10.1016/j.gore.2021.100898
Descripción
Sumario:Uterine arteriovenous malformations (AVMs) are rare and potentially life-threatening. They can be congenital or acquired. Uterine artery embolization or hysterectomy are considered mainstays of management. AVMs can be associated with leiomyomas, and patients may require both procedures. We present a case of a 42-year-old woman with a massively enlarged leiomyomatous uterus supplied and drained by multiple large AVMs, leading to high cardiac output state with severe four chamber cardiac dilation. Management required a multidisciplinary team of interventional radiology, gynecologic oncology surgery, vascular surgery, cardiac anesthesiology, cardiology, and urology and a 2-day interventional approach of preoperative arterial embolization followed by hysterectomy.