儿童和青少年阴积水的mri分层和外科治疗。

IF 1.4 3区 医学 Q2 PEDIATRICS
Amr AbdelHamid AbouZeid, Hany Emad Elhady, Shaimaa Abdelsattar Mohammad, Mohammad Seada, Osama El-Naggar, Mostafa Mohamed Elghandour
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引用次数: 0

摘要

在这篇报道中,我们提出了一种基于MRI发现的阴道梗阻(阴道积水)的新的解剖学分层,同时将梗阻的水平与固定的骨标记(耻骨联合)联系起来。这种新方法可以克服当前分类的局限性,这些分类在测量过程中容易出现近似误差,并且无法解释不同年龄组的体重变化。方法:回顾性分析诊断为阴道梗阻的病例资料。排除阴囊伴阴道梗阻的病例。MRI证实了诊断,并在正中矢状面将阴道梗阻相对于耻骨联合的水平分为低、中、高,分别相对于耻骨联合的下、中、上端。结果:2010年至2024年期间,13名女孩出现阴道梗阻。年龄在1个月至14岁之间(平均54个月;中位数:18个月)。三例出现在新生儿期与产前诊断的水肠。而6例在婴儿期/儿童期从其他中心转介。另一组青春期少女(4例)以隐经临床表现。阴道梗阻的原因为处女膜闭锁1例,阴道闭锁6例,持续性泌尿生殖窦5例,半阴道梗阻1例。在这个系列中,6例(46%)具有与遗传综合征相关的特征(Bardet Biedl/ McKusick-Kaufman谱)。在Bardet - Biedl综合征的其他综合征特征中,3例存在慢性实质肾脏疾病,另外1例伴有左肾缺失的左半阴道梗阻(herlin - werner - wunderlich综合征)。手术方法包括单纯切除远端阻塞膜4例,腹部辅助阴道成形术2例,阴道拉通术4例,单纯阴道成形术1例,泌尿生殖道窦动员术1例,半阴道梗阻术1例,纵向阴道间隔分割术。3例中至高位梗阻发生阴道狭窄或回缩,其中2例在腹部辅助阴道成形术后发生,1例在阴道拉通后发生。结论:以耻骨联合为参考,以mri为基础的阴道梗阻分层为手术计划提供了一种实用且可重复的方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
MRI-based Stratification and Surgical Management of Hydrocolpos in Children and Adolescents.

Introduction:  In this report we present a new anatomical stratification for vaginal obstruction (hydrocolpos) based on MRI findings while referring the level of obstruction to a fixed bony landmark (the pubic symphysis). This new approach can overcome the limitations of current classifications, which are prone to approximation errors during measurement and fail to account for variations in body mass across different age groups.

Methods:  Data of cases diagnosed with vaginal obstruction were retrospectively analyzed. Cases of cloaca with vaginal obstruction were excluded. MRI confirmed the diagnosis and enabled classification of the level of vaginal obstruction relative to the pubic symphysis in the mid-sagittal plane as low, intermediate, or high-opposite the lower, mid, or upper end of the pubic symphysis, respectively.

Results:  A total of 13 girls presented with vaginal obstruction during the period 2010 through 2024. Their age ranged between 1 month and 14 years (mean: 54 months; median: 18 months). Three cases presented in the neonatal period with antenatal diagnosis of hydrocolpos, while six cases were referred later during infancy/childhood from other centers. Another group of adolescent girls (four cases) presented with a clinical picture of cryptomenorrhea. The cause of vaginal obstruction was imperforate hymen in one, vaginal atresia in six, persistent urogenital sinus (five cases), and one case of obstructed hemi-vagina. In this series, six cases (46%) had features related to genetic syndromes (Bardet Biedl/ McKusick-Kaufman spectrum). Chronic parenchymatous renal disease was present in three cases among other syndromic features of Bardet Biedl syndrome, in addition to another case with obstructed left hemi-vagina that had absent left kidney (Herlyn-Werner-Wunderlich syndrome). Surgical techniques included simple excision of distal obstructing membrane (four cases), abdominal assisted vaginoplasty (two cases), vaginal pull-through (four cases), simple introitoplasty (one case), urogenital sinus mobilization (one case), and division of longitudinal vaginal septum for a case of obstructed hemi-vagina. Vaginal stenosis or retraction occurred in three cases with intermediate to high-level obstruction-two following abdominal assisted vaginoplasty and one after vaginal pull-through.

Conclusion:  MRI-based stratification of vaginal obstruction using the pubic symphysis as a reference provides a practical and reproducible approach for surgical planning.

Type of study and level of evidence:  This is a case series (level IV evidence).

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来源期刊
CiteScore
3.90
自引率
5.60%
发文量
66
审稿时长
6-12 weeks
期刊介绍: This broad-based international journal updates you on vital developments in pediatric surgery through original articles, abstracts of the literature, and meeting announcements. You will find state-of-the-art information on: abdominal and thoracic surgery neurosurgery urology gynecology oncology orthopaedics traumatology anesthesiology child pathology embryology morphology Written by surgeons, physicians, anesthesiologists, radiologists, and others involved in the surgical care of neonates, infants, and children, the EJPS is an indispensable resource for all specialists.
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