一例罕见的83岁跨性别女性:甲状腺激素缺乏是否与跨性别和性别焦虑症有关?

A. Frolov, Lauren Polcaro, C. Lawson, Yun-xi Tan, J. R. Martin
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引用次数: 0

摘要

在当前的报告中,我们描述了一名83岁的男性,他通过合法地将自己的名和中间名改为女性而自我认定为女性,他的死亡证明表明他的性别是女性。这名患者的病史显示完全阴茎切除术,但没有进一步说明。死后体检发现阴茎缺失,阴囊大,尿道口移位,睾丸小。睾丸的组织学分析发现,精小管的异常上皮缺乏生殖细胞和支持细胞,间质没有间质细胞存在。使用下一代测序(NGS) Illumina平台对个体DNA的外显子组测序显示,没有与阴茎或尿道癌相关的遗传变异可以解释完全阴茎切除术,但指出潜在的T3和T4甲状腺激素的产生受损,这可能解释观察到的睾丸畸形。总的来说,获得的数据提出了一个重要的问题,即甲状腺激素轴是否可能是支持男性性行为的激素结构的重要组成部分。
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A Rare Case of 83-Year-Old Transgender Female: Can Thyroid Hormone Deficiency Be Involved in Transgenderism and Gender Dysphoria?
In the current report, we describe an 83-year-old biological male who self- identified as a female by legally changing his first and middle names to female ones and whose death certificate states his sex as a female. The medical history of this individual indicated complete penectomy without further specification. Postmortem physical examination revealed an absence of penis with a large scrotum, transposed urethral orifice, and small testes. The histological analysis of the testes identified abnormal epithelium in the seminiferous tubules that lacked germ and Sertoli cells as well as the interstitium without Leydig cells present. The exome sequencing of the individual’s DNA using the Next Generation Sequencing (NGS) Illumina platform revealed no genetic variants associated with either penile or urethral cancer that could have explained the complete penectomy, but pointed toward a potentially impaired production of T3 and T4 thyroid hormones which could account for the observed testicular malformation. Overall, the data obtained raise an important question as to whether the thyroid hormone axis could be an important part of the hormonal architecture supporting male sexual behavior.
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