导致原发性闭经的 Mayer-Rokitansky-Küster-Hauser 综合征:病例报告

S. Kirami, S. Outaghyame, A. Diani, M. Benzalim, S. Alj
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引用次数: 0

摘要

Mayer-Rokitansky-Küster-Hauser(MRKH)综合征是一种罕见的先天性疾病,其特征是第二性征正常的女性没有子宫和上三分之二的阴道。我们介绍了一例 35 岁的原发性闭经妇女的病例,她的盆腔核磁共振成像在诊断 MRKH 综合征中发挥了关键作用,因为它发现了一个不发育的子宫和正常的卵巢。影像学检查,尤其是核磁共振成像,对于准确诊断和评估相关异常至关重要,可确保对该病症进行全面评估。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Mayer-Rokitansky-Küster-Hauser Syndrome as a Cause of Primary Amenorrhea: A Case Report
Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome is a rare congenital disorder marked by the absence of the uterus and upper two-thirds of the vagina in women with normal secondary sexual characteristics. We present the case of a 35-year-old woman with primary amenorrhea, where pelvic MRI played a crucial role in diagnosing MRKH syndrome by revealing a rudimentary uterus and normal ovaries. Imaging, particularly MRI, is essential for accurate diagnosis and assessment of associated abnormalities, ensuring a comprehensive evaluation of this condition.
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