Minimally invasive management of Müllerian anomalies in pediatric patients: A retrospective case series and literature review

Mario Riquelme , Juan Pelayo , Irving Cardenas-Medina , Ana Cantu-Zendejas , Alejandro Cendejas-Higuera , Eduardo Olazabal , Mario Palafox
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Abstract

Müllerian anomalies (MA) are structural defects that arise due to alterations in the development of the paramesonephric or Müllerian ducts during the first 16 weeks of gestation. Few cases have been reported on laparoscopic management as a diagnostic and therapeutic method in Müllerian anomalies. This study presents a retrospective case series of 9 patients diagnosed with Müllerian anomalies. A diagnostic approach was performed on 9 patients with suspected Müllerian anomalies, including 3 patients with OHVIRA Syndrome. Of all patients, 8 of them were treated with minimally invasive procedures, and one delayed the treatment. Our findings highlight the importance of employing advanced imaging techniques, such as MRI and UroCT, in complex cases to ensure accurate diagnosis and optimal surgical planning. Our case series demonstrates that most patients can have their condition successfully managed through a minimally invasive approach, as highlighted in the reported cases. Future studies should focus on expanding the clinical evidence base, focusing on long-term follow-up to assess fertility outcomes, quality of life and durability of these surgical interventions.
小儿穆勒氏畸形的微创治疗:回顾性病例系列和文献综述
勒氏管异常(MA)是指在妊娠的前16周内,由于副肾管或腰勒氏管的发育改变而引起的结构性缺陷。很少有病例报道腹腔镜管理作为诊断和治疗方法的 lererian异常。本研究回顾了9例诊断为勒氏管异常的患者。对9例疑似勒氏管异常患者进行了诊断,其中3例为OHVIRA综合征。所有患者中,8例采用微创手术治疗,1例延迟治疗。我们的研究结果强调了在复杂病例中采用先进成像技术(如MRI和UroCT)以确保准确诊断和最佳手术计划的重要性。我们的病例系列表明,大多数患者可以通过微创方法成功地控制病情,正如所报道的病例所强调的那样。未来的研究应侧重于扩大临床证据基础,侧重于长期随访,以评估这些手术干预的生育结局、生活质量和持久性。
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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