Huang Yuting, Loo Nicole M, Chang Alice Y, Yu Zachary, McKenna Amanda L, Ritchie Charles, Metcalfe Allie M, Nakhleh Raouf E, Krishna Murli, Taner C Burcin, Yang Liu
Division of Gastroenterology and Hepatology, Department of Internal Medicine, Mayo Clinic, Jacksonville, FL.
Department of Transplantation, Mayo Clinic, Jacksonville, FL.
ACG Case Rep J. 2024 Sep 11;11(9):e01483. doi: 10.14309/crj.0000000000001483. eCollection 2024 Sep.
The management of hepatic adenoma in transgender individuals undergoing gender-affirming hormone therapy remains unclear, especially whether treatment should be based on sex assigned at birth or therapy patient received. We presented a transgender man, female at birth, with hepatic adenomatosis with molecular profile differed from typical adenomas in cisgender males on testosterone. Discontinuing testosterone led to autoinfarction of the adenoma, allowing the avoidance of invasive treatments and resumption of gender-affirming hormone therapy. This case underscores the necessity for personalized care in the growing transgender population and challenges current consensus of treatment based on sex assigned at birth, emphasizing a tailored approach.
对于接受性别确认激素治疗的跨性别者,肝腺瘤的管理仍不明确,特别是治疗是否应基于出生时指定的性别或患者接受的治疗。我们报告了一名出生时为女性的跨性别男性,患有肝腺瘤病,其分子特征与接受睾酮治疗的顺性别男性中的典型腺瘤不同。停用睾酮导致腺瘤自动梗死,从而避免了侵入性治疗并恢复了性别确认激素治疗。该病例强调了在不断增长的跨性别群体中进行个性化护理的必要性,并挑战了目前基于出生时指定性别的治疗共识,强调了量身定制的方法。