Schneider Derek, Scully Kevin, Quintos Jose Bernardo, Millington Kate
Department of Pediatrics, The Warren Alpert Medical School of Brown University, Providence, RI 02903, USA.
Division of Pediatric Endocrinology and Diabetes, Hasbro Children's Brown University Health, Providence, RI 02903, USA.
JCEM Case Rep. 2025 Sep 9;3(10):luaf186. doi: 10.1210/jcemcr/luaf186. eCollection 2025 Oct.
The development of gender identity takes place under the influence of a complex interplay of social, psychological, and biological factors. Studies in individuals with disorders of sex development have suggested that exposure to androgens during fetal development and across the lifespan may contribute to a more masculine gender identity. We describe here an individual designated female at birth who presented with severe hyperandrogenism (total testosterone 337 ng/dL, 11.7 nmol/L) (reference range, 6-50 ng/dL [0.21-1.74 nmol/L]) and virilization secondary to polycystic ovarian syndrome in the setting of gender identity exploration. On presentation the patient endorsed a masculine gender identity, and after GnRH analog therapy reduced total testosterone to the cisgender female range, endorsed a feminine gender identity. This case adds to what is known about the possible range of androgen excess in polycystic ovarian syndrome and demonstrates the diagnosis and treatment of polycystic ovarian syndrome in a gender diverse adolescent.
性别认同的发展是在社会、心理和生物学因素复杂相互作用的影响下发生的。对性发育障碍个体的研究表明,胎儿发育期间及整个生命周期暴露于雄激素可能有助于形成更具男性化的性别认同。我们在此描述一名出生时被指定为女性的个体,该个体在进行性别认同探索时,因多囊卵巢综合征出现严重高雄激素血症(总睾酮337 ng/dL,11.7 nmol/L)(参考范围,6 - 50 ng/dL [0.21 - 1.74 nmol/L])和男性化表现。就诊时患者认可男性性别认同,在促性腺激素释放激素(GnRH)类似物治疗使总睾酮降至顺性别女性范围后,认可女性性别认同。该病例补充了我们对多囊卵巢综合征中雄激素过量可能范围的认识,并展示了对一名性别多样化青少年多囊卵巢综合征的诊断和治疗。