46,XY纯性腺发育不良伴自发性乳房发育、月经和双侧输卵管积水的罕见病例成功受孕和分娩

Q4 Medicine
K. Nadkarni
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引用次数: 1

摘要

目的:探讨46XY纯性腺发育不良(Swyer综合征)的异常表现、延迟诊断的意义、核型和早期性腺切除术的重要性以及ART的妊娠结局。背景:报告一例伴有自发性乳房发育、月经和双侧输卵管积水的Swyer综合征,并成功妊娠结局。病例描述:30岁女性,原发不孕症,继发闭经,第二性征正常。超声显示子宫小,卵巢萎缩,B/L输卵管积水。激素谱显示促性腺功能亢进性性腺功能减退,核型46XY。行腹腔镜输卵管切除术和性腺切除术。组织病理学显示无恶性迹象的条纹性腺,诊断为46XY性发育障碍(DSD)/ Swyer综合征。经乙炔雌二醇子宫内膜制备后,患者异位卵母细胞受孕,31周顺产早产双胞胎。结论:Swyer综合征患者多出现在青春期,伴青春期延迟和/或原发性闭经。然而,他们可以出现晚期继发性闭经或只是不规则,不频繁的月经或原发性不孕。在这种情况下,核型是强制性的,早期的性腺切除术可以提高长期生存率,因为性腺发育不良的恶性肿瘤发病率很高。在第二性征正常的患者中,早期恶性肿瘤通常是雌激素的来源。发育不全的子宫在扩大和子宫内膜准备方面对雌激素治疗有反应,而且子宫可能对分娩过程有反应,这些患者可以顺产。临床意义:早期诊断和及时处理性腺发育不良患者很重要。同种异体卵母细胞可以怀孕。需要进行遗传咨询和长期随访。ijifm
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Successful Conception and Delivery in an Unusual Case of 46,XY Pure Gonadal Dysgenesis with Spontaneous Breast Development, Menses, and Bilateral Hydrosalpinx
Aim: To study unusual presentations of 46XY pure gonadal dysgenesis (Swyer syndrome), implications of delayed diagnosis, importance of karyotype and early gonadectomy and pregnancy outcome with ART. Background: To report a case of Swyer syndrome with spontaneous breast development, menses and bilateral hydrosalpinx with Successful pregnancy outcome. Case description: 30 years old lady presented with primary infertility, secondary amenorrhea and normal secondary sexual characters. Sonography revealed small uterus with atrophic ovaries and B/L hydrosalpinx. Hormonal profile showed hypergonadotrophic hypogonadism and Karyotype was 46XY. Laparoscopic salpingectomy and gonadectomy was done. Histopathology revealed streak gonads with no evidence of malignancy and diagnosis of 46XY disorder of sexual development (DSD)/ Swyer syndrome was made. After endometrial preparation with ethinyl estradiol, patient conceived with allogenic oocytes and delivered preterm twins vaginally at 31 weeks. Conclusion: Patients with Swyer Syndrome usually present at adolescence with delayed puberty and/or primary amenorrhea. However they can present late with secondary amenorrhea or just irregular, infrequent menses or primary infertility. Karyotype is mandatory in such cases and early gonadectomy improves long term survival as incidence of malignancy in the dysgenetic gonad is high. Incipient malignancy is usually the source of estrogen in patients with normal secondary sexual characters. Hypoplastic uterus is responsive to estrogen therapy in terms of enlargement and endometrial preparation and also this uterus may have the ability to respond to the process of labor and these patients can deliver vaginally. Clinical significance: Early diagnosis and timely management of patients with dysgenetic gonads is important. Pregnancy is possible with allogenic oocytes. Genetic counseling and long term follow-up is required. ijifm
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CiteScore
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