Renal arteriovenous malformation and venous thrombosis: a tumour-like presentation

2021 ◽  
Vol 14 (11) ◽  
pp. e245602
Author(s):  
Fares Kosseifi ◽  
Martin Brenier ◽  
Isabelle Boulay ◽  
Xavier Durand

Renal arteriovenous malformation is a primarily congenital renal vascular abnormality. It is usually diagnosed incidentally on imaging, and the most common subtype is ‘cirsoid’, consisting of multiple, enlarged arterial feeders interconnecting with draining veins. We present a 74-year-old woman with an incidental finding of what was at first considered a hypervascularised kidney tumour but turned out to be a left intrarenal arteriovenous malformation associated with a left renal vein thrombosis. Selective endovascular embolisation was performed. The cause-consequence relationship between the arteriovenous malformation and the thrombosis is unique. To our knowledge, no such case has ever been reported.

2020 ◽  
Vol 54 (3) ◽  
pp. 297-300 ◽  
Author(s):  
Thomas Frederick Barge ◽  
Emma Wilton ◽  
Andrew Wigham

A 23-year-old presenting with an acute history of back pain, leg swelling, and claudication was diagnosed with an extensive iliocaval thrombosis, extending from the popliteal veins into the inferior vena cava (IVC) and left renal vein. He was treated with a combination of endovascular techniques, including EKOS and AngioJet. An underlying congenital IVC stenosis and May-Thurner type iliac vein compression were subsequently treated with venoplasty and stenting. To our knowledge, this is the first report of the use of EKOS for renal vein thrombosis and we highlight the complementary nature of different endovascular techniques for managing complex venous thrombotic disease.


2016 ◽  
Vol 2 (2) ◽  
pp. 20150218 ◽  
Author(s):  
Elisa Melo Abreu ◽  
Teresa Margarida Cunha

2013 ◽  
Vol 2013 ◽  
pp. 1-3 ◽  
Author(s):  
Faouzi Mallat ◽  
Wissem Hmida ◽  
Mehdi Jaidane ◽  
Nadia Mama ◽  
Faouzi Mosbah

Isolated renal vein thrombosis is a rare entity. We present a patient whose complaint of flank pain led to the diagnosis of a renal vein thrombosis. In this case, abdominal computed tomography angiography was helpful in diagnosing the nutcracker syndrome complicated by the renal vein thrombosis. Anticoagulation was started and three weeks later, CTA showed complete disappearance of the renal vein thrombosis. To treat the Nutcracker syndrome, we proposed left renal vein transposition that the patient consented to.


2011 ◽  
Vol 41 (2) ◽  
pp. 211-212 ◽  
Author(s):  
S. A. Puthiyaveetil ◽  
A. Mathew

1972 ◽  
Vol 107 (4) ◽  
pp. 517-520 ◽  
Author(s):  
J.E. Bernie ◽  
W.E. Friedel ◽  
R. Fernandez ◽  
H. Schutte

2014 ◽  
Vol 2014 (jan20 1) ◽  
pp. bcr2013202237-bcr2013202237 ◽  
Author(s):  
G. R. Nana ◽  
M. Basra ◽  
D. D. Maudgil ◽  
A. R. Rao

2015 ◽  
Vol 2015 ◽  
pp. 1-4 ◽  
Author(s):  
Moez Kdous ◽  
Oussema Khlifi ◽  
Marwene Brahem ◽  
Mohamed Khrouf ◽  
Sarah Amari ◽  
...  

Antenatal renal vein thrombosis is a rarely described diagnostic finding, with variable consequences on kidney function. We present the case of an affected fetus, born at 35-week gestation, with intrauterine oligohydramnios and two small kidneys. A renal ultrasound carried out after birth confirmed the presence of prenatal abnormalities. Renal vein thrombosis was not diagnosed at the time. The baby died 20 days later of kidney failure, metabolic acidosis, and polypnea with severe hypotrophy. Autopsy revealed atrophied kidneys and adrenal glands. The vena cava had thrombosis occupying most of its length. The right renal vein was normal, while the left renal vein was threadlike and not permeable. Histologically, there was necrosis of the left adrenal gland with asymmetrical bilateral renal impairment and signs of ischemic and hemorrhagic lesions. A review of thrombophilia was carried out and a heterozygous mutation in Factor V was found in both the mother and the child.


1971 ◽  
Vol 38 (6) ◽  
pp. 265-271
Author(s):  
A. Troitz ◽  
D. Meiraz ◽  
M. Ben-Bassat ◽  
I. Garti ◽  
J. Lazebnik

2014 ◽  
Vol 20 (2) ◽  
pp. 145-148
Author(s):  
Hyeon Jeong Yun ◽  
Jin Uk Jeong ◽  
Jong Ho Shin ◽  
Jin Ho Choi ◽  
Young Min Na ◽  
...  

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