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Complete androgen insensitivity syndrome: a case report and literature review
Min Guo1, Jin-Cheng Huang1, Cui-Fen Li1
1Department of Gynaecology, SSL Central Hospital of Dongguan City, Dongguan, Guangdong Province, China.
Abstract:
Complete androgen insensitivity syndrome (CAIS) is a rare disease that can be easily misdiagnosed. Before puberty, this condition is easily misdiagnosed as an inguinal hernia. This case report describes a 31-year-old phenotypically female patient with CAIS who was misdiagnosed twice previously with an inguinal hernia. Her karyotype analysis showed that she was 46, XY. She underwent a bilateral gonadectomy and long-term hormone replacement therapy. A Leydig cell tumour of the right testis was diagnosed postoperatively. This report also reviews the current understanding of the diagnosis and treatment of CAIS.
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