Department of Pediatric Surgery, Bambino Gesù Pediatric Hospital, Piazza di Sant'Onofrio, 4, Roma 00165, Italy; University of Rome Tor Vergata, Via Cracovia, 50, Roma 00133, Italy.
Department of Pediatric Surgery, Bambino Gesù Pediatric Hospital, Piazza di Sant'Onofrio, 4, Roma 00165, Italy.
J Pediatr Surg. 2022 Nov;57(11):696-701. doi: 10.1016/j.jpedsurg.2022.04.002. Epub 2022 Apr 15.
OHVIRA (Obstructed Hemivagina and Ipsilateral Renal Anomaly or Herlyn-Werner-Wunderlich syndrome) is a rare Müllerian malformation. Usually, symptoms begin with worsening dysmenorrhea in post-menarche adolescents. The management in pre-menarche period is controversial and has only recently been subject of study.
To review the experience of a pediatric tertiary center and to propose an age-specific management protocol for patients diagnosed before menarche.
A retrospective cohort study (review of medical records - period 2009-2021).
Twenty-eight patients were diagnosed (mean age 11.9 years), seven (25%) before menarche, one (3%) perinatally. One patient had Floating-Harbor syndrome. Twenty-three patients had ipsilateral renal agenesis, while five had a multicystic-dysplastic kidney. The contralateral kidney showed hypertrophy in 25 patients, pelvicalyceal ectasia in 8 and dysplasia in 1. Twenty-four patients were symptomatic. Three of the seven diagnosed prior to menarche had symptoms. All post-menarche diagnosed patients were symptomatic. Twenty-six patients underwent surgery (one-stage drainage, vaginal septal resection, and vaginoplasty). Asymptomatic pre-menarche patients were followed-up until surgery after menarche onset. No patient underwent surgery prior to menarche solely for OHVIRA diagnosis. At follow-up (median 3.5 years, 3 lost to follow-up), eighteen patients were asymptomatic, one developed endometriosis, one had impaired renal function, two needed reoperations.
Pre-menarche OHVIRA patients, without symptoms, should undergo regular follow-up until the onset of menarche. Surgery must be considered in post-menarche or symptomatic patients. Post-operative, long-term follow-up is required, evaluating both renal and gynecological issues.
LEVEL-OF-EVIDENCE: IV.
OHVIRA(单侧半隔阴道和同侧肾脏异常或 Herlyn-Werner-Wunderlich 综合征)是一种罕见的 Müllerian 畸形。通常,症状始于初潮后的青春期少女痛经加重。在初潮前的治疗存在争议,且直到最近才成为研究的主题。
回顾小儿三级中心的经验,并为诊断为初潮前的患者提出特定年龄的管理方案。
回顾性队列研究(病历回顾-2009 年至 2021 年期间)。
共诊断出 28 例患者(平均年龄 11.9 岁),其中 7 例(25%)在初潮前,1 例(3%)在围产期。1 例患者患有漂浮港综合征。23 例患者同侧肾脏发育不全,5 例患者多囊性发育不良肾脏。对侧肾脏在 25 例患者中出现肥大,在 8 例患者中出现肾盂积水,在 1 例患者中出现发育不良。24 例患者有症状。7 例在初潮前诊断的患者中有 3 例有症状。所有初潮后诊断的患者均有症状。26 例患者接受了手术(一期引流、阴道隔切除术和阴道成形术)。无症状的初潮前患者在初潮后开始手术前进行随访。没有患者在初潮前仅因 OHVIRA 诊断而接受手术。在随访(中位数 3.5 年,3 例失访)时,18 例患者无症状,1 例发生子宫内膜异位症,1 例肾功能受损,2 例需要再次手术。
无症状的初潮前 OHVIRA 患者应在初潮前进行定期随访。必须考虑对初潮后或有症状的患者进行手术。需要进行术后长期随访,评估肾脏和妇科问题。
IV。