A Case Report of Complete Androgen Insensitivity Syndrome Complicated with Dysgerminoma

doi:10.12280/gjfckx.20240083

Abstract

Abstract:

Androgen insensitivity syndrome (AIS) is rare and difficult to diagnose at an early stage. This paper reports the diagnosis and treatment of a patient with complete androgen insensitivity syndrome (CAIS) complicated with dysgerminoma. The patient was admitted to the hospital due to abdominal distension for 2 days and received color ultrasound in the outpatient department indicating pelvic tumor. After admission, pelvic tumor resection was performed. Since the cause of hyperandrogenemia was unknown before surgery, it was diagnosed as CAIS complicated with dysgerminoma by chromosome analysis and genetic testing, finally underwent radical resection of gonadal malignant tumor. At present, the patient is still under close follow-up and his condition is stable. Through retrospective analysis of the clinical characteristics and diagnosis and treatment of this case, in order to improve the clinical understanding of the disease.

Key words: Androgen-insensitivity syndrome, Disorders of sex development, Dysgerminoma, Hyperandrogenism, Case reports

YIN Yu-xin, WANG Chang-he. A Case Report of Complete Androgen Insensitivity Syndrome Complicated with Dysgerminoma[J]. Journal of International Obstetrics and Gynecology, 2024, 51(4): 392-394.

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