Background: Renal arteriovenous malformation (AVM) is a very rare phenomenon (fewer than 200 cases in the literature), most commonly (75%) presenting with hematuria in young women. Renal AVMs may be cirsoid (multibranched) or cavernous, with cirsoid morphology predominating 3:1. The historical treatment is partial nephrectomy. Best endovascular therapy is divided among many options. We present 2 cases of large renal AVMs treated with single Amplatzer plugs.
Methods: During a 2-year period (2014-15), 2 patients presented for vascular evaluation of renal AVMs found incidentally on workup for nonspecific abdominal and back pain. Both were the less common cavernous-type AVM. Each noted back pain ipsilateral to the AVM. Neither had a history of trauma or renal procedures. Each underwent angiography and Amplatzer plug placement to occlude flow while preserving parenchyma.
Results: Each patient successfully underwent occlusion of the arterial feeding branch of the AVM with immediate angiographic success. Each patient subsequently underwent follow-up imaging that demonstrated absence of filling of the AVM with preservation of healthy renal parenchyma.
Conclusions: Renal AVMs, although very rare, do present to vascular surgeons and may be managed successfully via an endovascular approach with standard techniques. Although renal AVMs are often managed with cyanoacrylate embolization, careful selective arterial catheterization allows for single plug embolization with excellent results and without requiring venous intervention.
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http://dx.doi.org/10.1016/j.avsg.2017.03.001 | DOI Listing |
Cureus
December 2024
Neurosurgery, Southmead Hospital, North Bristol NHS, Bristol, GBR.
Cerebral arteriovenous malformations (AVMs) are tangles of abnormal vessels with early arteriovenous (AV) shunting that can lead to intracerebral hemorrhage, seizures, neurologic deficit, or headache. To date, only a few cases of carcinomas metastasizing to pre-existing cerebral AVMs have been reported in the literature. However, renal clear cell carcinoma (RCC) brain metastases that exhibit early AV shunting, where AVM pathology is not present, are extremely rare.
View Article and Find Full Text PDFCureus
July 2024
Department of General, Vascular, Endocrine and Transplant Surgery, Medical University of Warsaw, Warsaw, POL.
Renal arteriovenous anomalies are uncommon. They are characterized by an abnormal vascular connection that usually bypasses the capillary bed. Most are acquired arteriovenous fistulas (AVF) while the rest are congenital or idiopathic arteriovenous malformations (AVM).
View Article and Find Full Text PDFFront Med (Lausanne)
May 2024
Department of Nuclear Medicine, the First College of Clinical Medical Science, China Three Gorges University, Yichang, Hubei, China.
Background: Renal arteriovenous malformations (rAVMs) are congenital abnormal pathways between renal arteries and veins that are rare in the general population. It is often misdiagnosed as malignant renal tumors with abundant blood supply, and the definitive diagnosis primarily relies on angiography. Multimodality imaging, including contrast-enhanced computed tomography (CT), magnetic resonance imaging (MRI), and positron emission tomography (PET)/CT plays an important role in the differential diagnosis of renal space-occupying lesions.
View Article and Find Full Text PDFCureus
April 2024
Emergency Department, Hiroshima City Hiroshima Citizens Hospital, Hiroshima, JPN.
J Surg Case Rep
May 2024
Division of Urology, Department Of Surgery, Ministry of The National Guard - Health Affairs, Riyadh, Saudi Arabia.
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