46, XY Disorders of Sexual Development: a case report and its theoretical framework

I. Brambilla, Enrico Landi, Carmen Guarracino, C. Pistone, Enrico Tondina, F. Sirchia, L. Avolio, P. Romano, S. Cavaiuolo, A. Licari, G. Riccipetitoni
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Abstract

Background and aim: Disorders of sexual differentiation (DSD) with karyotype 46,XY include gonadal developmental differences such as complete gonadal dysgenesis, partial gonadal dysgenesis, testicular regression and ovotesticular sexual differentiation disorder, differences in androgen synthesis or action, such as androgen synthesis deficiency, androgen action deficits, LH receptor deficiency, AMH synthesis or action deficits, and other conditions such as severe hypospadias, cloaca estrophy, etc. Methods: A 17 years-old girl came to our attention for hirsutism, clitoral hypertrophy, primary amenorrhea, and bilateral mammary hypoplasia. According to clinical features and anamnesis, the diagnosis of 46, XY DSD was made. For diagnostic purposes, she underwent an extensive genetic analysis, hormone dosage and instrumental examinations. After a clitoridoplasty and hormone replacement treatment, the patient performs appropriate multidisciplinary follow-up and regular psychotherapy. Results: The clinical case reported falls, according to the recent classification developed by the Chicago Consensus, within the scope of DSD with karyotype 46, XY. About 160 cases of patients with 17β-HSD3 deficiency, diagnosed at a mean age of 12 years, are described in the literature, most of them coming from Western Asia and Europe and only three cases from Eastern Asia. Clinically, about 30% of patients showed virilization, 20% clitoromegaly, ambiguous genitalia, inguinal/labial mass, 16% primary amenorrhea, and 5% absence of mammary development, features that are partly traced in the case described here. Conclusions: This case underscores the complexity of managing individuals with DSD. Having acquired the concept that irreversible surgery should be avoided, except in cases where failure to do so would determine health risks, the primary objective of the medical decision lies in meeting conditions aimed at harmonious sexual identification, especially regarding sexual activity and fertility, involving a team of experienced professionals (psychologists, pediatricians, surgeons, endocrinologists, radiologists), capable of promptly identifying suggestive clinical signs. (www.actabiomedica.it).
性发育障碍:一例报告及其理论框架
背景和目的:核型为46、XY的性分化障碍(DSD)包括性腺发育差异,如完全性腺发育障碍、部分性腺发育障碍、睾丸退行和卵睾丸性分化障碍;雄激素合成或作用差异,如雄激素合成不足、雄激素作用不足、LH受体不足、AMH合成或作用不足;以及其他情况,如重度尿道下裂、泄殖腔萎缩等。方法:一名17岁女孩因多毛、阴蒂肥大、原发性闭经及双侧乳腺发育不全而就诊。根据临床特点和记忆,诊断为46,xy型DSD。为了诊断目的,她接受了广泛的基因分析、激素剂量和仪器检查。在阴蒂成形术和激素替代治疗后,患者进行适当的多学科随访和定期心理治疗。结果:临床病例报告下降,根据芝加哥共识最近发展的分类,DSD的核型46,XY的范围内。文献报道了约160例17β-HSD3缺乏症患者,平均诊断年龄为12岁,其中大部分来自西亚和欧洲,只有3例来自东亚。临床上,约30%的患者表现为男性化,20%阴蒂肿大,阴唇模糊,腹股沟/阴唇肿块,16%原发闭经,5%乳腺未发育,这些特征在本病例中有部分体现。结论:本病例强调了管理DSD患者的复杂性。在认识到应避免不可逆转的手术,除非不这样做会确定健康风险的情况下,医疗决定的主要目标是满足旨在和谐的性别识别的条件,特别是在性活动和生育方面,由经验丰富的专业人员(心理学家、儿科医生、外科医生、内分泌学家、放射科医生)组成的团队参与,能够迅速识别暗示的临床迹象。(www.actabiomedica.it)。
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