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非那雄胺口服治疗女性变男性易性症患者雄激素性脱发的治疗经验。

Therapeutic experience with oral finasteride for androgenetic alopecia in female-to-male transgender patients.

作者信息

Moreno-Arrones O M, Becerra A, Vano-Galvan S

机构信息

Dermatology Department, Hospital Universitario Ramon y Cajal, Madrid, Spain.

出版信息

Clin Exp Dermatol. 2017 Oct;42(7):743-748. doi: 10.1111/ced.13184. Epub 2017 Jul 10.

Abstract

BACKGROUND

Androgenic treatment of female-to-male transgender patients may result in androgenetic alopecia (AGA). Use of 5-alpha-reductase inhibitors are useful as oral treatment of AA in men. There are no previous studies of the use of finasteride in transgender men as treatment of AGA.

AIM

To evaluate the effectiveness and safety of an oral 5α-reductase inhibitor (finasteride) for AA developed in transgender men.

METHODS

This single-centre retrospective study enrolled female-to-male transgender patients with a clinical diagnosis of AGA to receive 1 mg of an oral type II 5α-reductase inhibitor for at least 12 months.

RESULTS

In all, 10 patients were included in the study. All the patients received a clinical diagnosis of male-pattern AGA, with 90% classified as stage IV on the Norwood-Hamilton scale. Mean onset of AGA was 3.25 years after the introduction of androgenic treatment, and 70% of the patients had a family history of AGA. All the patients improved one grade on the Norwood-Hamilton scale after a mean of 5.5 months (range 4-6 months) since the start of finasteride treatment. Two patients stopped treatment for economic reasons and one stopped due to dyspepsia. No sexual or other adverse effects were observed. Patients were given periodic physical and analytical examinations by endocrinologists without any significant finding. Mean follow-up of patients was 16.2 months.

CONCLUSION

AA in transgender men has a delayed onset, and is clinically and therapeutically similar to the common male-pattern-AGA in cis-gender men.

摘要

背景

对女性向男性转变的跨性别患者进行雄激素治疗可能会导致雄激素性脱发(AGA)。5α-还原酶抑制剂可用于男性AGA的口服治疗。此前尚无关于非那雄胺用于跨性别男性治疗AGA的研究。

目的

评估口服5α-还原酶抑制剂(非那雄胺)对跨性别男性发生的AGA的有效性和安全性。

方法

这项单中心回顾性研究纳入了临床诊断为AGA的女性向男性转变的跨性别患者,给予1毫克口服II型5α-还原酶抑制剂,治疗至少12个月。

结果

该研究共纳入10例患者。所有患者均临床诊断为男性型AGA,90%在诺伍德-汉密尔顿量表上被归类为IV期。AGA的平均发病时间为雄激素治疗开始后3.25年,70%的患者有AGA家族史。自非那雄胺治疗开始后,平均5.5个月(范围4 - 6个月),所有患者在诺伍德-汉密尔顿量表上改善了一个等级。2例患者因经济原因停止治疗,1例因消化不良停止治疗。未观察到性方面或其他不良反应。内分泌科医生对患者进行了定期体格检查和分析检查,未发现任何重大异常。患者的平均随访时间为16.2个月。

结论

跨性别男性的AGA发病较晚,在临床和治疗上与顺性别男性常见的男性型AGA相似。

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