| Literature DB >> 10445308 |
M Tanaka1, K Iida, S Matsumoto, T Takeuchi, K Yamaguchi, Y Nishimura, T Tominaga.
Abstract
BACKGROUND: Congenital pelvic arteriovenous malformation (AVM) is rare especially in males. We present a case of pelvic AVM in a 38-year-old male. He was admitted to our hospital with left flank abdominal pain and painless gross hematuria. METHODS/DISCUSSION: Pelvic computed tomography demonstrated a homogeneous contrast-enhanced mass, 6 cm in diameter. For diagnosis, non-invasive magnetic resonance imaging (MRI) and color Doppler ultrasonography were very useful in our case. Though the treatment is controversial, we decided to monitor his clinical course.Entities:
Mesh:
Year: 1999 PMID: 10445308 DOI: 10.1046/j.1442-2042.1999.00077.x
Source DB: PubMed Journal: Int J Urol ISSN: 0919-8172 Impact factor: 3.369