Malhotra Neena, Dadhwal Vatsla, Sharma Kandala Aparna, Gupta Deepika, Agarwal Sumita, Deka Dipika
Department of Obstetrics and Gynecology, All India Institute of Medical Sciences, New Delhi, India.
J Turk Ger Gynecol Assoc. 2015 Nov 2;16(4):252-6. doi: 10.5152/jtgga.2015.15061. eCollection 2015.
Swyer syndrome, also known as 46 XY pure gonadal dysgenesis, is a rare endocrine disorder. Affected individuals are phenotypically female with female genitalia, normal Mullerian structures, absent testicular tissue, and a 46 XY chromosomal constitution. We report a series of eight cases of Swyer syndrome, of which six were managed by laparoscopic gonadectomy. The two other cases had to undergo an exploratory laparotomy in view of their presentation with adnexal masses. Two of the girls were siblings. The chief presenting complaint was primary amenorrhea. Four girls also presented with a history of poor development of secondary sexual characters. The average age at presentation was 16.19±2.85 years. The average height was 158.33 ±4.63 cm, and the average weight was 49.33±8.44 kg. Breast development was either Tanner 2 or 3 in four girls, whereas three girls had a Tanner 1 underdeveloped breasts. Axillary and pelvic hair was sparse in all the girls. The vagina was well canalized in all the girls. Hormonal evaluation revealed hypergonadotropic hypogonadism with a mean follicle-stimulating hormone (FSH) level of 95.81 mIU/L and a mean luteinizing (LH) level of 24.15 mIU/L. Imaging analysis revealed the presence of a small uterus in all the cases, except one. Bilateral ovaries were either not visualized or streak gonads were present. Adnexal mass was detected in two of the six cases with raised carcinoembryonic antigen (CA) 125 levels in one case. Genetic analysis revealed a karyotype of 46 XY in six girls, 46 XY/45 X in one, and the culture repeatedly failed in one girl. Because of the risk of malignancy, bilateral gonadectomy was performed in all cases. Histopathological analysis revealed that three of the six cases had dysgerminoma. The patients have been started on hormone replacement therapy. Laparoscopy is a minimally invasive modality for the definitive diagnosis and treatment of cases with Swyer syndrome. An early diagnosis of Swyer syndrome is possible during workup for primary amenorrhea before they present with adnexal masses.
斯维尔综合征,也称为46 XY单纯性腺发育不全,是一种罕见的内分泌疾病。受影响的个体在表型上为女性,具有女性生殖器、正常的苗勒管结构、无睾丸组织,以及46 XY染色体组成。我们报告了一系列8例斯维尔综合征病例,其中6例通过腹腔镜性腺切除术进行治疗。另外2例因附件肿块就诊而不得不接受剖腹探查术。其中2名女孩是姐妹。主要就诊主诉为原发性闭经。4名女孩还伴有第二性征发育不良史。就诊时的平均年龄为16.19±2.85岁。平均身高为158.33±4.63厘米,平均体重为49.33±8.44千克。4名女孩的乳房发育为坦纳2期或3期,而3名女孩的乳房发育为坦纳1期,发育不全。所有女孩的腋毛和阴毛均稀疏。所有女孩的阴道均通畅良好。激素评估显示高促性腺激素性性腺功能减退,平均促卵泡生成素(FSH)水平为95.81 mIU/L,平均促黄体生成素(LH)水平为24.15 mIU/L。影像学分析显示,除1例病例外,所有病例均存在小子宫。双侧卵巢要么未显影,要么存在条索状性腺。6例病例中有2例检测到附件肿块,其中1例癌胚抗原(CA)125水平升高。基因分析显示,6名女孩的核型为46 XY,1名女孩为46 XY/45 X,1名女孩的培养多次失败。由于存在恶变风险,所有病例均进行了双侧性腺切除术。组织病理学分析显示,6例病例中有3例患有无性细胞瘤。患者已开始接受激素替代治疗。腹腔镜检查是确诊和治疗斯维尔综合征病例的一种微创方式。在原发性闭经的检查过程中,在出现附件肿块之前,有可能早期诊断斯维尔综合征。