scholarly journals Intraparenchymal renal artery pseudoaneurysm following nephrostomy tube insertion in a patient with a solitary kidney: A case report

2021 ◽  
Vol 34 ◽  
pp. 101471
Author(s):  
A. Artiles-Medina ◽  
M. Hevia-Palacios ◽  
I. Laso-García ◽  
G. Duque-Ruiz ◽  
F. Arias-Funez ◽  
...  
2014 ◽  
Vol 66 (6) ◽  
pp. 719-722 ◽  
Author(s):  
Jahangir Beig ◽  
Imran Hafeez ◽  
Nisar Ahmed Tramboo ◽  
Hilal Rather ◽  
Irfan Yaqoob

BMC Urology ◽  
2021 ◽  
Vol 21 (1) ◽  
Author(s):  
Alec Zhu ◽  
Peter Connolly ◽  
A. Ari Hakimi

Abstract Background A renal artery aneurysm is a rare clinical presentation that can be found incidentally on imaging or during workup for refractory hypertension. Its presentation can be similar to that of a renal artery pseudoaneurysm, but the etiologies of the two vascular lesions differ. We present a patient who had an incidental finding of a large renal artery aneurysm that was managed with endovascular embolization. We also describe the literature surrounding the etiology, presentation and management of both renal artery aneurysms and renal artery pseudoaneurysms. Case presentation A 62-year-old man was referred to a urologic oncologist for workup of a newly found renal mass. Initial imaging with computed tomography showed a homogenous, well-circumscribed mass arising from the right kidney. Further evaluation with Doppler ultrasonography demonstrated pulsatile flow within the renal mass that was concerning for a renal artery pseudoaneurysm. The patient initially underwent a diagnostic angiogram by interventional radiology and was found to have a true renal artery aneurysm. Interventional radiology considered placement of a covered stent or angioembolization, but treatment was deferred due to concern for compromising the patient’s renal function. Patient was subsequently transferred to a neighboring hospital for management by vascular surgery. After considering both open surgical and endovascular approaches, the patient ultimately underwent angioembolization of the renal artery aneurysm. Short-term follow-up showed successful exclusion of the aneurysm with minimal adverse effects to the patient. Conclusions Our case report documents a unique case of an incidentally found large renal artery aneurysm that was successfully managed with endovascular embolization. Renal artery aneurysms and renal artery pseudoaneurysms, which can present similarly on imaging, are important diagnostic considerations in a patient presenting with a new renal mass. While open surgical approaches can be used to repair aneurysms, endovascular approaches using stenting or angioembolization are safe and effective options for treating renal aneurysms and renal pseudoaneurysms.


2009 ◽  
Vol 49 (1) ◽  
pp. 214-216 ◽  
Author(s):  
Jaap-Peter Schuurman ◽  
Jean Paul P.M. de Vries ◽  
Jan Albert Vos ◽  
Jan Wille

2018 ◽  
Vol 8 (6) ◽  
pp. 232-236 ◽  
Author(s):  
Yazin Marie ◽  
Avneesh Kumar ◽  
Sarah Hinchliffe ◽  
Simon Curran ◽  
Peter Brown ◽  
...  

2017 ◽  
Vol 2017 ◽  
pp. 1-4 ◽  
Author(s):  
Daniel Benamran ◽  
Benedicte de Clippele ◽  
Frank Hammer ◽  
Bertrand Tombal

Pseudoaneurysm and arteriovenous fistulae of the renal artery are rare complications of kidney trauma. They commonly result from open traumas and occur within days after the injury. Common symptoms include acute haematuria, pain, or hypertension. We report the case of a fifty-three-year-old man presenting with symptomatic complex chronic high flow kidney arteriovenous fistula with interposition of a pseudoaneurysmal pouch and arterial aneurysmal dilatation in a solitary left kidney 38 years after a blunt trauma. Those conditions were successfully treated by endovascular embolization followed by regular radiologic, biological, and clinical follow-up. To the best of our knowledge, few similar cases were reported more than 20 years after trauma. However, no case combining an arteriovenous fistula and a pseudoaneurysm revealing as late as 38 years after trauma was found. In addition, management of those conditions on a solitary kidney and outcomes has not been described. We believe that our case depicts the clinical presentation and management of this rare entity that should not be unrecognized due to its potential lethal implications.


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