baricitinib对斑秃和免疫性血小板减少症的双重改善:1例报告。

Q3 Medicine
Skin health and disease Pub Date : 2025-01-22 eCollection Date: 2025-02-01 DOI:10.1093/skinhd/vzae019
Chelsea Moon, Sarah E Park, Jennifer L Hsiao, Katrina H Lee
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引用次数: 0

摘要

口服Janus激酶(JAK)抑制剂baricitinib被美国食品和药物管理局批准用于治疗斑秃(AA)。我们报告一例AA和免疫性血小板减少症(ITP)的双重改善与口服巴西替尼单药治疗,这可能提示相关的自身免疫病理生理。在baricitinib治疗AA的III期临床试验中,报告的罕见不良血液学事件包括中性粒细胞减少症和贫血。虽然血液学合并症的历史可能会引起许多临床医生在考虑使用JAK抑制剂治疗时的关注,但这一临床小插曲表明,对于合并AA和ITP的患者,可以考虑巴西替尼,并且巴西替尼是安全的。一名56岁男性,有AA、ITP和白癜风病史,因类固醇抵抗性脱发复发而就诊,此前曾用托法替尼治疗。在与患者血液科医生协商后,在密切监测血小板的情况下,开始每日使用巴西替尼2mg,然后在6个月的随访中血小板出现改善后,将剂量加倍至4mg。开始使用巴西替尼14个月后,观察到白色和深色头发再生的改善,血小板保持正常。因此,baricitinib可用于AA和ITP的双重治疗,定期监测血小板并与血液科同事共同管理。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Dual improvement of alopecia areata and immune thrombocytopenia with baricitinib: a case report.

The oral Janus kinase (JAK) inhibitor baricitinib is approved by the U.S. Food and Drug Administration for the treatment of alopecia areata (AA). We report a case of dual improvement of AA and immune thrombocytopenia (ITP) with oral baricitinib monotherapy, which may suggest linked autoimmune pathophysiology. In phase III clinical trials of baricitinib for AA, reports of rare adverse haematological events include neutropenia and anaemia. While a history of haematological comorbidities may raise concern for many clinicians when considering treatment with a JAK inhibitor, this clinical vignette suggests that baricitinib may be considered and safely administered in those with concomitant AA and ITP. A 56-year-old man with a history of AA, ITP and vitiligo presented to the clinic for relapse of his steroid-resistant hair loss which had previously been treated with tofacitinib. In consultation with the patient's haematologist, baricitinib 2 mg daily was started with close platelet monitoring then doubled to 4 mg after platelets showed improvement at the 6-month follow-up. Fourteen months after initiating baricitinib, improvement in white and dark hair regrowth was observed, and platelets remained normal. Thus, baricitinib may be considered for the dual treatment of AA and ITP with regular platelet monitoring and co-management with haematology colleagues.

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CiteScore
1.70
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