巴比替尼应用后并发肺外结核1例。

Tetsuro Shimada, Akira Maeyama, Tomonobu Hagio, Kunihide Muraoka, Terufumi Shibata, Yutaro Yamasaki, Taiga Oda, Makoto Hamasaki, Takuaki Yamamoto
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引用次数: 1

摘要

使用Janus激酶(JAK)抑制剂治疗的患者可发生肺外结核(TB)。我们报告一例类风湿关节炎合并肺外结核后巴氏替尼治疗。一名45岁的日本女性在另一家医院被诊断为类风湿关节炎,随后她开始在我们研究所接受甲氨蝶呤(MTX) 6.0 mg/周和强的松龙3.0 mg/天的治疗。MTX剂量增加至10mg /周,达到临床缓解;然而,疾病活动在初次就诊6个月后突然爆发。在T-SPOT®结核病筛查呈阳性后开始使用异烟肼(INH)预防,由于对MTX的反应不足,3周后开始使用巴西替尼(Olumiant®)。INH预防持续6个月。开始INH治疗10个月后,在患者颈部左侧观察到无痛性肿块。磁共振示淋巴结肿大伴钙化。随后的活检和病理检查诊断为结核性淋巴结炎,并开始对患者进行抗结核治疗。10个月后,患者病情仍在缓解,情况良好。肺外结核可能难以诊断,因为物理和实验室检查结果不一致。当使用JAK抑制剂治疗患者时,医生应该认识到发展为肺外结核的可能性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A case of extrapulmonary tuberculosis after use of baricitinib.

Extrapulmonary tuberculosis (TB) can occur in patients treated with Janus kinase (JAK) inhibitors. We present a case of rheumatoid arthritis complicated by extrapulmonary TB following baricitinib treatment. A 45-year-old Japanese woman was diagnosed with rheumatoid arthritis at another hospital, and she subsequently started treatment with methotrexate (MTX) at 6.0 mg/week and prednisolone at 3.0 mg/day at our institute. The MTX dose was increased to 10 mg/week, and clinical remission was achieved; however, the disease activity flared up 6 months after the initial visit. Isoniazid (INH) prophylaxis was started following positive T-SPOT® screening for TB, and baricitinib (Olumiant®) was introduced 3 weeks later because of an insufficient response to MTX. INH prophylaxis was continued for 6 months. Ten months after starting INH treatment, a painless mass was observed on the left side of the patient's neck. Magnetic resonance imaging showed enlarged lymph nodes with calcification. A subsequent biopsy and pathologic examination led to a diagnosis of tuberculous lymphadenitis, and the patient was started on anti-TB therapy. Ten months later, the patient was still in remission and doing well. Extrapulmonary TB can be difficult to diagnose because of inconsistent physical and laboratory findings. When treating patients with JAK inhibitors, physicians should be cognisant of the potential for extrapulmonary TB to develop.

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