Congenital uterovaginal prolapse in a term neonate: a case report

IF 0.2 Q4 PEDIATRICS
Jejaw Endale , Yidnekachew Getachew , Samuel Gashu , Belachew Dejene , Mihret S. Tesfaye , Hiwot Y. Anley
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Abstract

Introduction

Congenital uterovaginal prolapse in neonates is a rare condition, and it is often associated with spinal cord defects.

Case presentation

A 3-day-old female term neonate born via cesarean section with a weight of 3.2 Kg was admitted to our pediatric surgery unit due to a protruding mass in the vaginal introitus and swelling in the lower back. On physical examination, the mass measured 4 by 5 cm was and appeared to be the vagina and part of the uterus. There was no discharge or bleeding. The mass was easily reducible but recurred when the patient cried. A spinal ultrasound confirmed a 3 by 2-cm defect in the lumbosacral area, consistent with a meningomyelocele. The patient also had bilateral clubfoot. A transfontanellar ultrasound showed obstructive hydrocephalus, likely due to aqueductal stenosis, and showed a small posterior fossa with an inferiorly displaced vermis, suggesting Chiari malformation type II. Several attempts at manual reduction and packing of the mass with a plaster were made but were unsuccessful. The patient was taken to the operating room for a vaginal cerclage. Two incisions were made on the vaginal wall at the 6 o'clock and 12 o'clock positions, approximately 1 cm above the fourchette. A circumferential suture of reabsorbable material was then placed and securely tied. The postoperative course was uneventful. The patient was subsequently transferred to the neurosurgery department for further evaluation and management. At three months of follow-up there have been no signs of tissue damage, and no recurrence of the prolapse.

Conclusion

Congenital uterovaginal prolapse is a rare anomaly, and most cases occur in patients with neural tube defects. Vaginal cerclage seems to be a safe and effective management option.
足月新生儿先天性子宫阴道脱垂1例
新生儿先天性子宫阴道脱垂是一种罕见的疾病,通常与脊髓缺陷有关。病例介绍:一名剖宫产出生的3天大的足月女婴,体重3.2 Kg,因阴道开口突出肿块和下背部肿胀而入住儿科外科。在体格检查中,这个4 × 5厘米的肿块是阴道和子宫的一部分。无分泌物或出血。肿块很容易缩小,但在病人哭泣时复发。脊柱超声证实腰骶区有一个3 × 2厘米的缺损,符合脊膜膨出。患者还患有双侧内翻足。经fontanellar超声显示梗阻性脑积水,可能是由于导水管狭窄,并显示一个小的后窝并下方移位的蚓部,提示II型Chiari畸形。多次尝试手工复位和用石膏包扎肿块,但均未成功。病人被带到手术室做阴道环切术。在阴道壁上6点钟和12点钟位置做了两个切口,大约在子宫四壁上方1厘米。然后放置可吸收材料的环状缝合线并牢固地绑好。术后过程平淡无奇。患者随后转至神经外科接受进一步评估和治疗。在三个月的随访中,没有组织损伤的迹象,也没有脱垂的复发。结论先天性子宫阴道脱垂是一种罕见的异常,多发生于神经管缺陷患者。阴道环扎术似乎是一种安全有效的治疗方法。
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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来源期刊
CiteScore
0.60
自引率
25.00%
发文量
348
审稿时长
15 days
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