机构地区:[1]中山大学孙逸仙纪念医院妇产科,广州510235
出 处:《中华妇幼临床医学杂志(电子版)》2022年第1期61-66,共6页Chinese Journal of Obstetrics & Gynecology and Pediatrics(Electronic Edition)
基 金:国家自然科学基金项目(81971332)。
摘 要:目的探讨完全型雄激素不敏感综合征(CAIS)和46,XY单纯性腺发育不全综合征(Swyer综合征)2种最常见46,XY女性性发育异常疾病(DSD)的临床特征、诊疗方式、鉴别诊断要点。方法选择2002—2020年,于中山大学孙逸仙纪念医院就诊的临床病例资料完整的41例46,XY DSD患者,包括20例CAIS(CAIS组)患者和21例Swyer综合征(Swyer组)患者。对该41例患者的临床表现、实验室检查结果、术中情况及组织病理学检查结果进行回顾性分析。本研究遵循的程序符合2013年新修订的《世界医学协会赫尔辛基宣言》要求。结果①41例46,XY DSD患者在出生及成长过程中的社会性别均为女性,就诊年龄为12~38岁。2组患者年龄比较,差异无统计学意义(P>0.05)。CAIS组患者身高、体重均高于或重于Swyer组,并且差异有统计学意义(P<0.05)。②2组患者血清卵泡刺激素(FSH)、睾酮、雌二醇、17α-羟孕酮(17α-OHP)水平比较,差异均有统计学意义(P<0.05);而2组血清促黄体激素(LH)、催乳素、脱氢表雄酮(DHEA)水平比较,则差异均无统计学意义(P>0.05)。CAIS组患者抗苗勒管激素(AMH)水平均>16 ng/mL,Swyer组均<0.03 ng/mL。③39例接受手术治疗患者中,35例行腹腔镜下性腺切除术,4例行开腹肿瘤细胞减灭术。④CAIS组患者性腺肿瘤发生率为35.0%(7/20),Swyer组为36.8%(7/19)。CAIS组患者性腺有自伞端向腹股沟管迁移趋势,其中4例性腺位于腹股沟管内,Swyer组患者性腺均位于盆腔内。⑤41位患者出院后,均继续以女性性别生活,已婚者性生活无障碍。结论CAIS与Swyer综合征患者临床表现相似,CAIS患者存在苗勒管遗迹,Swyer综合征患者存在子宫发育不良等变异,并且均有不同程度的性腺迁移趋势。AMH水平检测可作为区别CAIS与Swyer综合征患者的特异性指标。Objective To explore clinical features,treatment and differential diagnosis of complete androgen insensitivity syndrome(CAIS)and 46,XY pure gonadal dysgenesis syndrome(Swyer syndrome),the two most common 46,XY female disorders of sex development(DSD)phenotypes.Methods From 2002 to 2020,a total of 41 cases of 46,XY DSD,including 20 cases of CAIS and 21 cases of Swyer syndrome diagonsed in Sun Yat-Sen Memorial Hospital were selected into this study.They were divided into CAIS group(n=21,CAIS patients)and Swyer group(n=21,Swyer patients).Their clinical manifestations,laboratory data,operative conditions and pathological results of the patients were analyzed by retrospective analysis method.The procedure followed in this study met requirements of the Helsinki Declaration of the World Medical Association revised in 2013.Results①All the 41 patients were born and raised up as female.The age at first visit was around 12 to 38 years old.There was no significant difference in age between two groups(P>0.05).The height and weight of CAIS group were significantly higher than those of Swyer group(P<0.05).②There were significantly differences in levels of serum follicle stimulating hormone(FSH),testosterone,estradiol and 17α-hydroxyprogesterone(17α-OHP)between two groups(P<0.05).There were no significant differences in serum luteinizing hormone(LH),prolactin and dehydroepiandrosterone(DHEA)between two groups(P>0.05).The levels of anti-mullerian hormone(AMH)in CAIS group were all>16 ng/mL,and those in Swyer group were all<0.03 ng/mL.③Among 39 cases received surgical treatment,35 cases underwent laparoscopic bilateral gonadectomy,4 cases underwent open cytoreductive surgery.④The incidences of gonadal tumor in CAIS group and Swyer group were 35.0%(7/20),36.8%(7/19),respectively.Gonads of CAIS patients tended to migrate from fimbria to inguinal canal and in Swyer group,all of gonads were located in pelvic cavity.Conclusions Both CAIS and Swyer syndrome belong to 46,XY DSD,the clinical phenotype is similar to some extent,s
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