Acién Pedro, Acién Maribel
Department of P.H., Sc.H. and Gynecology/Division of Gynecology, Miguel Hernández University, San Juan Campus, 03550, San Juan, Alicante, Spain.
Obstetrics and Gynecology Service, San Juan University Hospital, San Juan, Spain.
Insights Imaging. 2016 Oct;7(5):713-26. doi: 10.1007/s13244-016-0515-4. Epub 2016 Aug 9.
To help physicians and radiologists in the diagnosis of female genito-urinary malformations, especially of complex cases, the embryology of the female genital tract, the basis for Müllerian development anomalies, the current classifications for such anomalies and the comparison for inclusion and cataloguing of female genital malformations are briefly reviewed. The use of the embryological system to catalogue female genito-urinary malformations may ultimately be more useful in correlations with clinical presentations and in helping with the appropriate diagnosis and treatment. Diagnostic imaging of the different genito-urinary anomalies are exposed, placing particular emphasis on the anomalies within group II of the embryological and clinical classification (distal mesonephric anomalies), all of them associated with unilateral renal agenesis or dysplasia. Similarly, emphasis is placed on cases of cervico-vaginal agenesis, cavitated noncommunicated uterine horns, and cloacal and urogenital sinus anomalies and malformative combinations, all of them complex malformations. Diagnostic imaging for all these anomalies is essential. The best imaging tools and when to evaluate for other anomalies are also analysed in this review.
• The appropriate cataloguing of female genital malformations is controversial. • An embryological classification system suggests the best diagnosis and appropriate management. • The anomalies most frequently diagnosed incorrectly are the distal mesonephric anomalies (DMAs). • DMAs are associated with unilateral renal agenesis or renal dysplasia with ectopic ureter. • We analyse other complex malformations. Diagnostic imaging for these anomalies is essential.
为帮助内科医生和放射科医生诊断女性生殖泌尿系统畸形,尤其是复杂病例,本文简要回顾了女性生殖道的胚胎学、苗勒管发育异常的基础、此类异常的当前分类以及女性生殖器畸形纳入和编目的比较。使用胚胎学系统对女性生殖泌尿系统畸形进行编目,最终可能在与临床表现的相关性以及帮助进行适当的诊断和治疗方面更有用。本文阐述了不同生殖泌尿系统异常的诊断性影像学检查,特别强调胚胎学和临床分类中第二组(远端中肾异常)的异常,所有这些异常都与单侧肾缺如或发育异常有关。同样,重点关注宫颈阴道发育不全、有空腔但不连通的子宫角、泄殖腔和泌尿生殖窦异常及畸形组合的病例,所有这些都是复杂畸形。对所有这些异常进行诊断性影像学检查至关重要。本综述还分析了最佳影像学工具以及何时评估其他异常。
• 女性生殖器畸形的适当编目存在争议。• 胚胎学分类系统有助于最佳诊断和适当管理。• 最常被误诊的异常是远端中肾异常(DMA)。• DMA与单侧肾缺如或伴有异位输尿管的肾发育异常有关。• 我们分析了其他复杂畸形。对这些异常进行诊断性影像学检查至关重要。