Complete Androgen Insensitivity Syndrome: Revisiting a Rarity—A Case Report

被引:0
|
作者
Jaspreet S. Sandhu
Madhulima S. Saha
Bhuvaneesh Sanbhu
机构
[1] Department of Urology,Department of Obstetrics and Gynaecology
[2] Bahrain Specialist Hospital,Department of Surgery
[3] Command Hospital Kolkata,undefined
[4] Command Hospital Kolkata,undefined
来源
Indian Journal of Surgery | 2022年 / 84卷
关键词
Complete androgen insensitivity syndrome (CAIS); Disorders of sexual development; Inguinal gonads; Primary Amenorrhea; Case report;
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中图分类号
学科分类号
摘要
Complete androgen insensitivity syndrome is a rare disorder. Primary amenorrhea beyond 14 years of age without, and 16 years along with developed secondary sexual characters should raise suspicion of this entity as a cause. Inguinal examination may confirm presence of inguinal gonads. The absence of female internal genitalia on imaging, absence of pubic/axillary hair, and chromosomal analysis clinch the diagnosis. Surgical excision of gonads to prevent malignancy, estrogen supplementation, and vaginoplasty along with psychological counselling remain the mainstay of treatment.
引用
收藏
页码:1089 / 1092
页数:3
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