一名男性盆腔动静脉畸形病例。
A case of pelvic arteriovenous malformation in a male.
作者信息
Tanaka M, Iida K, Matsumoto S, Takeuchi T, Yamaguchi K, Nishimura Y, Tominaga T
机构信息
Department of Urology, Mitsui Memorial Hospital, Tokyo, Japan.
出版信息
Int J Urol. 1999 Jul;6(7):374-6. doi: 10.1046/j.1442-2042.1999.00077.x.
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.
背景
先天性盆腔动静脉畸形（AVM）较为罕见，尤其是在男性中。我们报告一例38岁男性盆腔AVM病例。他因左侧腹疼痛和无痛性肉眼血尿入院。
方法/讨论：盆腔计算机断层扫描显示一个直径6厘米的均匀强化肿块。对于诊断，无创磁共振成像（MRI）和彩色多普勒超声在我们的病例中非常有用。尽管治疗存在争议，但我们决定监测他的临床病程。
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