Uterine Arteriovenous Malformation Presenting with Amenorrhea-A Rare Case Report and Literature Review.

IF 0.8 Q3 MEDICINE, GENERAL & INTERNAL
Hanna Gruber, Dirk O Bauerschlag, Chie-Hee Cho, Aimée B Herzog, Ibrahim Alkatout, Melanie Schubert
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Abstract

Background and Clinical Significance: Uterine arteriovenous malformation (AVM) is a rare but potentially life-threatening condition due to the risk of severe acute hemorrhage. Unlike AVMs in other anatomical locations, which are predominantly congenital, uterine AVMs are often acquired, typically developing after uterine procedures such as dilatation and curettage (D&C), cesarean section, or pregnancy-related events. Women commonly present with abnormal bleeding disorders. Case Presentation: We are presenting the case of a 41-year-old Caucasian woman with secondary amenorrhea three months after vacuum curettage in the 7th week of pregnancy. Based on her clinical history and the findings on transvaginal sonography (TVS), uterine AVM was highly suspected. Contrast-enhanced magnetic resonance imaging (MRI) confirmed the diagnosis. The patient underwent successful embolization of the left uterine artery. Follow-up examinations demonstrated complete resolution of the vascular malformation, and regular menstrual cycles resumed during her recovery. With the increasing frequency of uterine surgical interventions, the incidence of uterine AVMs is also expected to rise. The clinical impact is significant when fertility preservation and family planning are still ongoing. To the best of our knowledge, this is the first reported case in which amenorrhea is the primary presenting symptom of a uterine AVM. Conclusions: Given the high risk of life-threatening hemorrhage associated with undetected or incorrectly treated AVMs, their presence must always be carefully ruled out in case of bleeding disorders after pregnancy or uterine surgery. Accurate diagnosis prior to any further intrauterine interventions, such as curettage, is crucial to prevent severe complications and ensure appropriate management. In order to avoid life-threatening complications, the possibility of uterine AVM should be considered in the differential diagnosis even in the presence of amenorrhea. The proposed diagnosis and treatment algorithm for uterine AVMs can help avoid misdiagnosis.

以闭经为表现的子宫动静脉畸形一例罕见报告并文献复习。
背景和临床意义:子宫动静脉畸形(AVM)是一种罕见但可能危及生命的疾病,由于严重的急性出血的风险。与其他解剖位置的avm主要是先天性的不同,子宫avm通常是获得性的,通常在子宫手术后发展,如扩张和刮除(D&C),剖宫产或妊娠相关事件。女性通常表现为异常出血性疾病。病例介绍:我们提出的情况下,41岁的白人妇女继发性闭经后三个月的真空刮除在怀孕第7周。根据她的临床病史和经阴道超声检查结果,高度怀疑子宫AVM。磁共振造影(MRI)证实了诊断。病人成功地栓塞了左子宫动脉。随访检查显示血管畸形完全消退,恢复期间月经周期正常。随着子宫手术介入频率的增加,子宫动静脉畸形的发生率也有望上升。当生育保留和计划生育仍在进行时,临床影响是显著的。据我们所知,这是第一例闭经是子宫AVM的主要症状。结论:考虑到未被发现或治疗不正确的动静脉畸形与危及生命的出血相关的高风险,在妊娠或子宫手术后出血障碍的情况下,必须始终仔细排除它们的存在。在任何进一步的宫内干预(如刮宫)之前进行准确诊断,对于预防严重并发症和确保适当管理至关重要。为了避免危及生命的并发症,即使在闭经的情况下,在鉴别诊断时也应考虑子宫AVM的可能性。本文提出的子宫动静脉畸形诊治算法有助于避免误诊。
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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