[A Case of Pelvic Arteriovenous Malformation in a Male with Massive Bladder Bleeding which Caused Severe Hemorrhagic Hypovolemic Shock].

Q4 Medicine Acta Urologica Japonica Pub Date : 2025-01-01 DOI:10.14989/ActaUrolJap_71_1_17
Takuro Miyagawa, Yuki Kita, Naoya Kani, Wataru Tanaka, Takahiro Yamaguchi, Yusuke Hama, Kyohei Sugiyama, Ryo Iguchi, Naoto Terai, Koji Inoue
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引用次数: 0

Abstract

Congenital arteriovenous malformation (AVM) in the male pelvis is extremely rare. We present a case of this disease with massive bladder bleeding which caused severe hemorrhagic shock. Diagnosis of pelvic AVM was confirmed by computed tomography and angiography. He was treated with transcatheter arterial embolization of the bilateral internal iliac arteries. We discuss the clinical course and the treatment for AVM in this case, and review the literature.

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[1例男性膀胱大出血并发骨盆动静脉畸形致严重出血性低血容量性休克]。
先天性动静脉畸形(AVM)在男性骨盆是非常罕见的。我们报告一例因膀胱大量出血而引起严重失血性休克的病例。通过计算机断层扫描和血管造影证实盆腔AVM的诊断。他接受了双侧髂内动脉经导管栓塞治疗。我们讨论该病例的临床过程和治疗方法,并复习文献。#农协。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Acta Urologica Japonica
Acta Urologica Japonica Medicine-Medicine (all)
CiteScore
0.20
自引率
0.00%
发文量
74
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