An XY Female.

Q3 Medicine
European journal of case reports in internal medicine Pub Date : 2025-03-24 eCollection Date: 2025-01-01 DOI:10.12890/2025_005277
Marwa Al-Qudheeby, Dhari Alharbi, Layal Alqaysi, Fatemah Alshaer, Lulwa Al-Enezi
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引用次数: 0

Abstract

Background: Primary amenorrhoea (PA) is defined as the lack of menstruation at age 13 years in the absence of normal growth and secondary sexual characteristics, or lack of menstruation at age 15 years in the setting of normal growth and secondary sexual characteristics. Most underlying causes of PA can be classified into gonadal, anatomic, endocrine and systemic causes. Disorders of sexual development (DSD) are a rare, yet challenging aetiology.

Case description: We present a 24-year-old, previously healthy female, who complained of PA and absent breast development. The patient denied any other symptoms. The physical examination revealed a tall girl, with infantile breasts and unambiguous female external genitalia, with no abnormalities. Laboratory tests showed hypogonadotropic hypogonadism (HH), undetectable anti Müllerian hormone (AMH), present Müllerian structures and absent ovaries in the pelvic magnetic resonance imaging (MRI), with a 46,XY karyotype. The abdominal and pelvic laparoscopy confirmed the presence of Müllerian structures, with no evidence of gonadal tissues. A diagnosis of early testicular regression syndrome (ETRS) was given. Hormonal replacement therapy (HRT) was started and escalated thereafter, resulting in regular menses, breast development and patient satisfaction.

Conclusion: PA in a 46,XY female is a challenging disorder. Although several differential diagnoses are considered, the unique clinical, hormonal, radiological and cytogenic findings are helpful in suggesting the diagnosis of ETRS.

Learning points: Primary amenorrhoea can be caused by defects at various levels.The disorders of sexual development are important, yet less frequent, causes of primary amenorrhoea.The successful management of primary amenorrhoea relies on a multidisciplinary approach.

一只XY型雌性。
背景:原发性闭经(PA)被定义为在没有正常生长和第二性征的情况下,13岁时月经不足,或在正常生长和第二性征的情况下,15岁时月经不足。大多数PA的潜在原因可分为性腺、解剖、内分泌和全身原因。性发育障碍(DSD)是一种罕见的,但具有挑战性的病因。病例描述:我们报告了一位24岁的健康女性,她主诉PA和乳房发育不全。病人否认有其他症状。体格检查显示,这是一个身材高大的女孩,有着婴儿般的乳房和明确的女性外生殖器,没有任何异常。实验室检查显示:促性腺功能减退(HH),未检测到抗勒氏体激素(AMH),盆腔磁共振成像(MRI)显示有勒氏体结构和未见卵巢,核型为46,xy。腹部和盆腔腹腔镜检查证实存在勒氏管结构,没有性腺组织的证据。诊断为早期睾丸退化综合征(ETRS)。激素替代疗法(HRT)开始并逐步升级,导致月经规律,乳房发育和患者满意度。结论:46,XY女性PA是一种具有挑战性的疾病。虽然考虑了几种鉴别诊断,但独特的临床,激素,放射学和细胞遗传学结果有助于建议诊断ETRS。学习要点:原发性闭经可由不同程度的缺陷引起。性发育障碍是原发性闭经的重要原因,但发生率较低。原发性闭经的成功治疗依赖于多学科联合治疗。
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
2.10
自引率
0.00%
发文量
166
审稿时长
8 weeks
期刊介绍: The European Journal of Case Reports in Internal Medicine is an official journal of the European Federation of Internal Medicine (EFIM), representing 35 national societies from 33 European countries. The Journal''s mission is to promote the best medical practice and innovation in the field of acute and general medicine. It also provides a forum for internal medicine doctors where they can share new approaches with the aim of improving diagnostic and clinical skills in this field. EJCRIM welcomes high-quality case reports describing unusual or complex cases that an internist may encounter in everyday practice. The cases should either demonstrate the appropriateness of a diagnostic/therapeutic approach, describe a new procedure or maneuver, or show unusual manifestations of a disease or unexpected reactions. The Journal only accepts and publishes those case reports whose learning points provide new insight and/or contribute to advancing medical knowledge both in terms of diagnostics and therapeutic approaches. Case reports of medical errors, therefore, are also welcome as long as they provide innovative measures on how to prevent them in the current practice (Instructive Errors). The Journal may also consider brief and reasoned reports on issues relevant to the practice of Internal Medicine, as well as Abstracts submitted to the scientific meetings of acknowledged medical societies.
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