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• W1995878312 abstract "Background The complete androgen insensitivity (testicular feminization) syndrome was described in phenotypic females with 46XY karyotype, presenting with primary amenorrhea, adequate breast development, and absent or sparse pubic or axillary hair. Gonads consist usually of seminiferous tubules without spermatogenesis. Case We report the case of a 15-year-old girl with testicular feminization since age 4. She was admitted to surgically remove the testes from the inguinal canal. Microscopic examination of the left testis revealed a Sertoli-Leydig cell tumor and the draft of fallopian tube with adjacent seminiferous tubules. Summary and Conclusion These patients have a 5%-10% risk of developing germ cell tumors. Sertoli-Leydig cell tumors are uncommon neoplasms, usually benign in testicular feminization syndrome." @default.
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• W1995878312 date "2014-10-01" @default.
• W1995878312 modified "2023-09-26" @default.
• W1995878312 title "Complete Androgen Insensitivity Syndrome with a Sertoli-Leydig Cell Tumor" @default.
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• W1995878312 doi "https://doi.org/10.1016/j.jpag.2013.08.007" @default.
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