Uterine arteriovenous malformation (AVM) is a rare condition, with fewer than 100 cases reported in the literature. Despite it being rare, it is a potentially life-threatening condition. This case report describes a 33-year-old woman who presented with secondary post-partum hemorrhage. Transabdominal ultrasound (US) of the pelvis showed increased vascularity with multidirectional flow of the uterus and a prominent vessel, located on the left lateral wall. She also had retained product of conception, which complicated the diagnosis. A uterine artery angiogram confirmed an AVM in the fundal region with an early draining vein. Embolisation of the AVM was performed successfully. © Penerbit Universiti Sains Malaysia, 2013.
CITATION STYLE
Hashim, H., & Nawawi, O. (2013). Uterine arteriovenous malformation. Malaysian Journal of Medical Sciences, 20(2), 77–81. https://doi.org/10.21613/gorm.2018.776
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