先天性肾上腺增生女婴子宫和卵巢的超声改变:假睾丸征

S. Alamdaran, Soroush Dehghani Dashtabi, Armin Vahabi Sani, Vakili Rahim, S. Hashemian
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引用次数: 0

摘要

背景:先天性肾上腺增生症(CAH)是导致阴唇模糊的主要原因之一。CAH患者内生殖器的异常外观与许多其他被归类为性发育障碍(DSD)的病症相似。本研究旨在准确描述CAH患者子宫和卵巢的诊断超声特征,以区分其与其他原因的生殖器模糊。方法:本横断面研究于2017 - 2020年在伊朗马什哈德医学大学阿克巴儿童医院进行。本研究记录了22例(2-60日龄)因21-羟化酶缺乏而发生CAH的女婴和47例年龄相近的健康婴儿的子宫和卵巢超声检查结果并进行了分析。结果:对照组除2例(95%)外,其余健康儿宫颈均正常突出。在病例组中,只有9例(41%)婴儿宫颈正常突出,其他13例新生儿的眼底和宫颈大小几乎相等。两组眼底/宫颈比值差异有统计学意义(P=0.009)。77%的患者双侧卵巢均无卵泡,而对照组中28%的健康婴儿无卵泡,其余为单侧或双侧多卵泡卵巢。治疗2个月后,所有患者均出现双侧多卵泡卵巢。非卵泡性卵巢征象(假睾丸外观)在病例组中更为普遍(P=0.004)。此外,一半的婴儿显示正常的盆腔淋巴结,由于其均匀的高回声质地,模仿睾丸样外观。结论:CAH女婴正常盆腔淋巴结和非卵泡性卵巢表现为睾丸样。注意这些常见的发现可以防止隐睾的误诊和进行其他实验室检查和核型的时间损失。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Ultrasonographic Changes of the Uterus and Ovaries in Female Infants with Congenital Adrenal Hyperplasia: Pseudo-Testicular Sign
Background: Congenital Adrenal Hyperplasia (CAH) is one of the main causes of ambiguous genitalia. The unusual appearance of internal genitalia in CAH patients is similar to many other conditions which are classified in Disorders of Sex Development (DSD). This study aimed to accurately describe diagnostic ultrasonic features of the uterus and ovaries in CAH patients in order to distinguish it from other causes of ambiguous genitalia. Methods: This cross-sectional study was performed in Akbar Children Hospital, Mashhad University of Medical Sciences, Mashhad, Iran, from 2017 to 2020. Ultrasound findings of the uterus and ovaries of 22 female infants (2-60 days of age) with CAH due to 21-hydroxylase deficiency and 47 healthy infants with a similar age were recorded and eventually analyzed in this study. Results: All the healthy infants in the control group had a normal prominent cervix, except for two neonates (95%). In the case group, only 9 (41%) infants had a normal prominent cervix, and other 13 newborns had nearly equal sizes of fundus and cervix. There was a significant difference between the two groups in the fundus-to-cervix ratio (P=0.009). The 77% patients had no follicles in both ovaries, while 28% healthy infants in the control group had no follicles, and the rest had unilateral or bilateral multi-follicular ovaries. After two months following treatment, bilateral multi-follicular ovaries were observed in all patients. The sign of non-follicular ovaries (pseudo-testicular appearance) was significantly more prevalent in the case group (P=0.004). Furthermore, half of infants showed normal pelvic lymph node that mimic a testicular-like appearance due to its uniform hyper-echoic texture. Conclusion: The testicular-like appearance of normal pelvic lymph nodes and non-follicular ovaries in a female infant with CAH. Attention to these usual findings can prevent misdiagnoses of cryptorchidism and time loss to perform other laboratory tests and karyotyping.
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