Arteriovenous malformation of the prostatic median lobe: a rare case treated by transurethral resection

Authors

  • Ibrahim Untan Department of Urology, Ahi Evran University, Training and Research Hospital, Kirsehir Turkey

DOI:

https://doi.org/10.47391/JPMA.6455

Abstract

Arteriovenous malformation localised to the prostate is rare. Until recently, the gold standard for diagnosis was angiography; however, this changed with the use of computed tomography and magnetic resonance imaging, which quickly became the first-line diagnostic tools. Common complaints are haematuria and lower urinary tract symptoms, for which there are no well-defined management guidelines. We present the case of a 53-year-old male patient who was treated for clotted haematuria. While the bleeding was thought to originate from an enlarged prostate, cystoscopy displayed a non-pulsatile, exophytic, active bleeding mass on the median lobe. The mass was resected transurethrally and diagnosed as arteriovenous malformation. This case shows an aberrant presentation of a vascular malformation in the prostate. The mass seemed to be constrained to a compact area without a visible plurality of arterial feeders. Since the prostate is a rare location for arteriovenous malformation, there are no well-defined treatment options.

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Published

2023-05-15

How to Cite

Ibrahim Untan. (2023). Arteriovenous malformation of the prostatic median lobe: a rare case treated by transurethral resection. Journal of the Pakistan Medical Association, 73(6), 1305–1307. https://doi.org/10.47391/JPMA.6455

Issue

Section

CASE REPORT