scholarly journals 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

2021 ◽  
Author(s):  
Taigo Kato
2014 ◽  
Vol 13 (5) ◽  
pp. 175
Author(s):  
A.D. Urbina Lima ◽  
A.B. Albano Del Pozo ◽  
J.J. Colombo Stenstrom ◽  
J. Murillo Mirat ◽  
A. Pijierro Amador ◽  
...  

1997 ◽  
Vol 58 (1) ◽  
pp. 55-57 ◽  
Author(s):  
Takao Kamai ◽  
Kazuo Saito ◽  
Makoto Hirokawa ◽  
Hiroshi Tukamoto ◽  
Hiroshi Ashida

2016 ◽  
Vol 45 (6) ◽  
pp. 306-312
Author(s):  
Kenjiro Kaneko ◽  
Makiko Omori ◽  
Hirotsugu Ozawa ◽  
Shigeki Hirayama ◽  
Yuji Kanaoka ◽  
...  

2010 ◽  
Vol 03 (01) ◽  
Author(s):  
Dimitrios S Tzortzakakis ◽  
Michael S Nomikos ◽  
Ioanna N Tritou ◽  
Adam A Hatzidakis ◽  
Ploutarchos E Anezinis

Urology ◽  
2019 ◽  
Vol 130 ◽  
pp. 211-212
Author(s):  
Charles Schlaepfer ◽  
Jonathan Weese ◽  
Daniel Picus ◽  
Ramakrishna Venkatesh

2008 ◽  
Vol 14 (2_suppl) ◽  
pp. 19-22 ◽  
Author(s):  
Chang-Hsien Ou ◽  
Ho-Fai Wong ◽  
Ming-Shiang Yang ◽  
Tzu-Hsien Yang ◽  
Tzu-Lung Ho

Endovascular embolization for craniofacial arteriovenous malformation has been used as preoperative adjuvant devascularization or as definitive therapy. However, because the vascular network is complex, embolization via arterial access may be ineffective, risky, incomplete or technically difficult. The purpose of this report is to describe our experience of percutaneous direct venous pouch puncture embolization. Four patients with craniofacial AVMs were treated with direct puncture embolization via injection of NBCA. After the selective transarterial angiogram, the lesions were directly punctured in the venous pouch under a road map angiogram. A glue mixture was injected, and post-embolization angiograms revealed that in all patients, the lesions had been completely obliterated without complication. Percutaneous direct puncture embolization is an effective, time saving and safe technique for the superficial craniofacial AVM with prominent venous pouch.


2019 ◽  
Vol 03 (02) ◽  
pp. 134-138
Author(s):  
Heather Kate Moriarty ◽  
Warren Clements ◽  
Tim Joseph ◽  
Anoop Madan ◽  
Tuan Phan

AbstractOccurrence of a symptomatic renal arteriovenous malformation (AVM) is rare. The authors present the case of a patient with a background of Turner's syndrome, hemophilia B, and horseshoe kidney, who presented with hematuria and was successfully treated with endovascular embolization. The use of a microballoon catheter Scepter XC (Microvention, Inc.) to safely embolize the feeding arterial supply, using ethylene vinyl alcohol (EVOH) copolymer (Onyx; Medtronic/ev3) has not, to the authors’ knowledge, previously been described for the treatment of renal AVM. This novel use of an occlusal balloon catheter is permitted by the precipitation rate of Onyx, and allowed a safe and effective procedure, reducing the risk of reflux, allowing a forward push of embolic material in a controlled manner.


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