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Complete Testicular Feminization Syndrome: a Case Report
Journal of the Korean Association of Pediatric Surgeons ; : 47-52, 2006.
Article in Korean | WPRIM | ID: wpr-131243
ABSTRACT
Testicular feminization syndrome (TFS) is a genetic disorder due to androgen insensitivity of the target organs. The most common clinical presentation of complete TFS is inguinal hernia in the infant or primary amenorrhea in the adolescence. A 7-year old phenotypically female patient was seen with a complaint of a right inguinal mass. Under the diagnosis of right inguinal hernia, high ligation was performed. Six months later, the patient showed a left inguinal mass. On operation, the mass looked like a testis. The external genitalia were normal female, but a uterus and ovary were not identified. Chromosome study showed a 46, XY karyotype and the levels of serum testosterone and dihydrotestosterone were increased after HCG stimulation. The patient was diagnosed as complete TFS and underwent bilateral gonadectomy 6 months later.
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Full text: Available Index: WPRIM (Western Pacific) Main subject: Ovary / Dihydrotestosterone / Androgen-Insensitivity Syndrome / Testis / Testosterone / Uterus / Diagnosis / Karyotype / Amenorrhea / Genitalia Type of study: Diagnostic study Limits: Adolescent / Child / Female / Humans / Infant / Male Language: Korean Journal: Journal of the Korean Association of Pediatric Surgeons Year: 2006 Type: Article

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Full text: Available Index: WPRIM (Western Pacific) Main subject: Ovary / Dihydrotestosterone / Androgen-Insensitivity Syndrome / Testis / Testosterone / Uterus / Diagnosis / Karyotype / Amenorrhea / Genitalia Type of study: Diagnostic study Limits: Adolescent / Child / Female / Humans / Infant / Male Language: Korean Journal: Journal of the Korean Association of Pediatric Surgeons Year: 2006 Type: Article