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Recurrent Urinary Retention Due to Clots Caused by a Congenital Renal Arteriovenous Malformation That Forms a Complex Vascular Network: Report of Two Cases

Overview
Journal IJU Case Rep
Date 2022 Jan 10
PMID 35005456
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Abstract

Introduction: Repeated urinary retention due to clots caused by congenital renal arteriovenous malformation is rare.

Case Presentation: A 40-year-old woman (case 1) and a 66-year-old man (case 2) experienced recurrent urinary retention due to clots. Neither patient had a history of renal trauma nor was taking any medications. Contrast-enhanced abdominal computed tomography revealed a large hematoma in the renal pelvis and ureter with no masses, stones, or vascular lesions and only dilated blood vessels in the arterial phase in case 1. Angiography of the kidney in both patients revealed an arteriovenous malformation, and embolization of the arteries feeding the arteriovenous malformation was performed. Soon after embolization, hematuria disappeared completely with no recurrence for 5 years in case 1 and 2 years in case 2.

Conclusion: Congenital renal arteriovenous malformation should be considered as a cause of recurrent clot retention, and angiographic embolization of the feeding arteries can be an effective treatment.

Citing Articles

Acute Abdominal Pain Without Gross Hematuria as an Atypical Initial Presentation of Renal Arteriovenous Malformation.

Iga K, Okazaki Y, Huh K, Ichiba T Cureus. 2024; 16(4):e59367.

PMID: 38817495 PMC: 11138708. DOI: 10.7759/cureus.59367.


Editorial Comment from Dr. Kato to Recurrent urinary retention due to clots caused by a congenital renal arteriovenous malformation that forms a complex vascular network: Report of two cases.

Kato T IJU Case Rep. 2022; 5(1):8-9.

PMID: 35005457 PMC: 8720722. DOI: 10.1002/iju5.12388.


Recurrent urinary retention due to clots caused by a congenital renal arteriovenous malformation that forms a complex vascular network: Report of two cases.

Ishii M, Nakata W, Horibe Y, Tsujimura G, Tsujimoto Y, Nin M IJU Case Rep. 2022; 5(1):5-8.

PMID: 35005456 PMC: 8720720. DOI: 10.1002/iju5.12368.

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