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首页> 外文期刊>Journal of Clinical Imaging Science >Congenital Uterine Arteriovenous Malformation Presenting as Postcoital bleeding: A Rare Presentation of a Rare Clinical Condition
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Congenital Uterine Arteriovenous Malformation Presenting as Postcoital bleeding: A Rare Presentation of a Rare Clinical Condition

机译:先天性子宫动静脉畸形表现为性交后出血:罕见的临床状况罕见表现

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Congenital uterine arteriovenous malformation (AVM) is an extremely rare condition with 100 cases documented in literature. We report multiparous women presenting to us with a history of postcoital bleed. Initial Doppler ultrasonography was consistent with features suggestive of AVM. Subsequently, computed tomography (CT) angiography confirmed the diagnosis. Embolization was chosen as the treatment because of the large extension of AVM and the risk of hemorrhage during hysterectomy. The patient was discharged in a stable condition with a plan of repeat embolization in the next setting. At 6 and 12 weeks of follow?up, she did not experience any further episodes of bleed. The purpose of this case report is to highlight the salient clinical features, diagnosis, and the management options available for this rare clinical condition.
机译:先天性子宫动静脉畸形(AVM)是一种极为罕见的疾病,文献记载的病例少于100例。我们报告了众多女性,这些女性向我们展示了性交后出血的历史。最初的多普勒超声检查与提示AVM的特征一致。随后,计算机断层扫描(CT)血管造影证实了诊断。选择栓塞术作为治疗方法是因为AVM扩展范围大,并且子宫切除术有出血的风险。患者在稳定的情况下出院,并计划在下一次重复栓塞。在随访的6周和12周时,她没有再出现任何出血事件。本病例报告的目的是强调针对这种罕见临床状况的主要临床特征,诊断和可用的治疗方案。

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