Case Report
Renal arteriovenous malformation: An unusual pathology
South African Journal of Radiology | Vol 23, No 1 | a1704 |
DOI: https://doi.org/10.4102/sajr.v23i1.1704
| © 2019 Alain M. Mukendi, Amer Rauf, Sean Doherty, Florence Mahlobo, Peter Afolayan, Shabina Dawadi
| This work is licensed under CC Attribution 4.0
Submitted: 16 December 2018 | Published: 30 May 2019
Submitted: 16 December 2018 | Published: 30 May 2019
About the author(s)
Alain M. Mukendi, Department of Urology, Chris Hani Baragwanath Academic Hospital, University of the Witwatersrand, Johannesburg, South AfricaAmer Rauf, Department of Radiology, Chris Hani Baragwanath Academic Hospital, University of the Witwatersrand, Johannesburg, South Africa
Sean Doherty, Department of Urology, Chris Hani Baragwanath Academic Hospital, University of the Witwatersrand, Johannesburg, South Africa
Florence Mahlobo, Department of Radiology, Chris Hani Baragwanath Academic Hospital, University of the Witwatersrand, Johannesburg, South Africa
Peter Afolayan, Department of Urology, Chris Hani Baragwanath Academic Hospital, University of the Witwatersrand, Johannesburg, South Africa
Shabina Dawadi, Department of Radiology, Chris Hani Baragwanath Academic Hospital, University of the Witwatersrand, Johannesburg, South Africa
Abstract
Renal arteriovenous malformations are rare renal vascular abnormalities. More commonly, the term refers to the congenital type of malformation. Only a few cases have ever been presented and reported in the literature, mostly with a nidus. We present the clinical, ultrasound and computed tomography findings and discuss the management related to a 63-year-old male with a right congenital renal arteriovenous malformation without a nidus that was successfully managed with coil embolisation. Relevant literature is hereby reviewed to highlight characteristic imaging and appropriate treatment.
Keywords
Renal vascular malformations; congenital renal arteriovenous fistula; vascular nidus; coil embolisation; endovascular management.
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