Infertility management in a patient with Swyer syndrome: a case report.

IF 2.7 3区 医学 Q2 GENETICS & HEREDITY Journal of Assisted Reproduction and Genetics Pub Date : 2025-05-01 Epub Date: 2025-03-18 DOI:10.1007/s10815-025-03442-4
Laura Krygere, Ruta Bartasiene, Agne Kozlovskaja-Gumbriene, Egle Drejeriene
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Abstract

Purpose: To highlight the successful use of assisted reproductive technologies in achieving pregnancy and healthy childbirth in a woman with Swyer syndrome, a rare disorder of sex development characterized by gonadal dysgenesis, elevated gonadotropin levels, oestrogen insufficiency, tall stature, delayed puberty, and primary amenorrhoea. This case highlights the efficacy of reproductive treatments for individuals with nonfunctional gonads resulting from complete gonadal dysgenesis.

Methods: This report describes a woman diagnosed with Swyer syndrome at 18 years, presenting with primary amenorrhoea and delayed puberty. Following diagnosis, the patient underwent bilateral gonadectomy due to the increased risk of germ cell neoplasia and began hormone replacement therapy to address oestrogen insufficiency. At 31, the patient pursued fertility treatment, undergoing in vitro fertilisation (IVF) with donated oocytes.

Results: The IVF treatment using donor oocytes led to a successful pregnancy without complications. The pregnancy culminated in the delivery of a healthy baby via caesarean section, marking a successful outcome for a patient with Swyer syndrome.

Conclusion: Assisted reproductive technologies, particularly in vitro fertilisation (IVF) using oocyte donation, provide a feasible option for individuals diagnosed with Swyer syndrome to achieve parenthood. This case adds to the growing research on reproductive success in women with complete gonadal dysgenesis, emphasizing the potential for positive outcomes through specific reproductive approaches.

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斯韦尔综合征患者的不孕症治疗:病例报告。
目的:强调辅助生殖技术在Swyer综合征患者妊娠和健康分娩中的成功应用。Swyer综合征是一种罕见的性发育障碍,其特征是性腺发育障碍、促性腺激素水平升高、雌激素不足、身材高大、青春期延迟和原发性闭经。本病例强调了生殖治疗对完全性腺发育不良导致性腺功能丧失的个体的疗效。方法:本报告描述了一位18岁时被诊断为Swyer综合征的女性,表现为原发性闭经和青春期延迟。诊断后,由于生殖细胞瘤的风险增加,患者接受了双侧性腺切除术,并开始激素替代治疗以解决雌激素不足。31岁时,患者继续进行生育治疗,用捐赠的卵母细胞进行体外受精(IVF)。结果:供体卵母细胞体外受精治疗成功妊娠,无并发症。这次怀孕最终通过剖腹产生下了一个健康的婴儿,标志着斯威耶综合征患者的成功结局。结论:辅助生殖技术,特别是使用卵母细胞捐赠的体外受精(IVF),为诊断为Swyer综合征的个体提供了一种可行的生育选择。该病例增加了对完全性腺发育不良妇女生殖成功的日益增长的研究,强调了通过特定的生殖方法获得积极结果的潜力。
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来源期刊
CiteScore
5.70
自引率
9.70%
发文量
286
审稿时长
1 months
期刊介绍: The Journal of Assisted Reproduction and Genetics publishes cellular, molecular, genetic, and epigenetic discoveries advancing our understanding of the biology and underlying mechanisms from gametogenesis to offspring health. Special emphasis is placed on the practice and evolution of assisted reproduction technologies (ARTs) with reference to the diagnosis and management of diseases affecting fertility. Our goal is to educate our readership in the translation of basic and clinical discoveries made from human or relevant animal models to the safe and efficacious practice of human ARTs. The scientific rigor and ethical standards embraced by the JARG editorial team ensures a broad international base of expertise guiding the marriage of contemporary clinical research paradigms with basic science discovery. JARG publishes original papers, minireviews, case reports, and opinion pieces often combined into special topic issues that will educate clinicians and scientists with interests in the mechanisms of human development that bear on the treatment of infertility and emerging innovations in human ARTs. The guiding principles of male and female reproductive health impacting pre- and post-conceptional viability and developmental potential are emphasized within the purview of human reproductive health in current and future generations of our species. The journal is published in cooperation with the American Society for Reproductive Medicine, an organization of more than 8,000 physicians, researchers, nurses, technicians and other professionals dedicated to advancing knowledge and expertise in reproductive biology.
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