Brown University, Department of Obstetrics and Gynecology, The Warren Alpert Medical School, Providence, RI, USA.
Brown University, Division of Pediatric Urology, Hasbro Children's Hospital, The Warren Alpert Medical School, Providence, RI, USA.
J Pediatr Urol. 2018 Apr;14(2):144-149. doi: 10.1016/j.jpurol.2018.01.011. Epub 2018 Feb 9.
Mullerian anomalies have a known association with renal agenesis yet, to date, there are no formal recommendations for screening women with certain renal anomalies for associated genital tract disorders.
The objective of this study is to review current data regarding the association between renal and Mullerian anomalies, and propose screening recommendations.
A comprehensive review of the literature was performed to identify relevant articles using the keywords "unilateral renal agenesis," "renal anomalies," and "Mullerian anomalies."
Over 30% of patients with unilateral renal agenesis have an associated Mullerian anomaly. However, diagnosis is frequently delayed in this population until after menarche when complications of retrograde menstruation with obstructive anomalies lead to significant problems including endometriosis, pelvic inflammatory disease, and infertility. No clear guidelines exist for communication among the antenatal sonographer, the obstetrician, the parents, and the child's pediatrician, which creates a barrier to effective screening and follow-up. Further, no current guidelines exist for screening women with certain renal anomalies for Mullerian anomalies.
The complications of Mullerian anomalies are easily preventable if identified early. We propose new guidelines for education and screening for Mullerian anomalies in patients with unilateral renal agenesis (URA) and multicystic dysplastic kidney (MCDK) to guide providers, patients, and parents on proper identification and management (Table).
Screening young women with URA and MCDK for Mullerian anomalies has the potential to prevent long-term complications from untreated obstructive malformations. Identification of unilateral renal agenesis on antenatal ultrasound must be clearly articulated with parents and the child's pediatrician so that proper screening can be performed before menarche. Pelvic sonography is a low-cost, high-yield screening tool to identify these anomalies.
苗勒管畸形与肾发育不全有已知的关联,但迄今为止,尚无针对特定肾畸形患者进行生殖道畸形相关筛查的正式建议。
本研究旨在回顾肾与苗勒管畸形之间的关联的现有数据,并提出筛查建议。
对文献进行全面综述,使用关键词“单侧肾发育不全”、“肾畸形”和“苗勒管畸形”来识别相关文章。
超过 30%的单侧肾发育不全患者存在相关的苗勒管畸形。然而,在该人群中,诊断通常会延迟到月经初潮后,此时由于梗阻性畸形导致逆行性月经引起的并发症会导致严重问题,包括子宫内膜异位症、盆腔炎和不孕。产前超声检查医师、产科医师、家长和儿科医生之间缺乏明确的沟通指南,这成为了有效筛查和随访的障碍。此外,目前也没有针对某些肾畸形患者进行苗勒管畸形筛查的指南。
如果早期发现,苗勒管畸形的并发症是可以预防的。我们提出了针对单侧肾发育不全(URA)和多囊性发育不良肾(MCDK)患者的苗勒管畸形教育和筛查的新指南,以指导提供者、患者和家长正确识别和管理(表)。
对患有 URA 和 MCDK 的年轻女性进行苗勒管畸形筛查有可能预防未治疗的梗阻性畸形引起的长期并发症。在产前超声检查中发现单侧肾发育不全时,必须与家长和患儿的儿科医生明确说明,以便在月经初潮前进行适当的筛查。盆腔超声是一种低成本、高收益的筛查工具,可用于识别这些畸形。