Literature DB >> 23249874

The origin of idiopathic renal arteriovenous malformation with giant twin aneurysms.

Yoshitaka Iwazu1, Shigeaki Muto, Yukio Miyata, Masanori Ochi, Akihiko Tokue, Yasushi Asano, Eiji Kusano.   

Abstract

A 50-year-old female patient who presented with intermittent gross hematuria was referred to our hospital. Three-dimensional computed tomography (3D-CT) revealed a left renal arteriovenous malformation (AVM). Because she declined to undergo additional therapy including surgical treatment, we observed the clinical course of renal AVM for 7 years using 3DCT. When the 3D-CT showed gradual enlargement of the aneurysms concurrent with the onset of clinical symptoms (cardiomegaly and hypertension), we performed simple left nephrectomy. After the operation, the cardiomegaly and hypertension returned to normal, and gross hematuria did not recur. Based on the macro-anatomical findings of the resected kidney and the observation of the natural course, this case strongly supported the hypothesis that the renal AVM had existed from birth and enlarged gradually to eventually produce the typical signs and symptoms.

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Year:  2013        PMID: 23249874     DOI: 10.5414/cn107228

Source DB:  PubMed          Journal:  Clin Nephrol        ISSN: 0301-0430            Impact factor:   0.975


  2 in total

1.  Treatment of Complex, Combined Renal Artery Aneurysm and Renal Arteriovenous Fistula with Nephrectomy.

Authors:  R W Franz; C F Tanga
Journal:  Int J Angiol       Date:  2016-04-03

2.  Renal arteriovenous malformation: An unusual pathology.

Authors:  Alain M Mukendi; Amer Rauf; Sean Doherty; Florence Mahlobo; Peter Afolayan; Shabina Dawadi
Journal:  SA J Radiol       Date:  2019-05-30
  2 in total

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