Pepeler Mehmet S, Özkurt Zübeyde N, Güzel Özlem T, Akyürek Nalan
Gazi University, Ankara,Turkey.
J Infect Dev Ctries. 2018 Oct 31;12(10):926-928. doi: 10.3855/jidc.9993.
Primary myelofibrosis (PMF) is a clonal stem cell disease, characterized by bone marrow fibrosis. Ruxolitinib is a selective inhibitor of JAK-1 and JAK-2 used to treat PMF. Its mechanism of action is based on the reduction of signal transduction and cytokine levels; including IL-6 and tumor necrosis factor alpha. Increased infection risk related to Ruxolutinib is rarely reported. Here we describe a case of tuberculosis infection ractivation in a female patient treated with Ruxolitinib. During the treatment, she complained of night sweats, weight loss and enlarged mass in the neck. Excisional mass biopsy revealed a necrotizing granulomatous lymphadenitis. QuantiFERON-TB and PPD tests were not able to diagnose the tuberculosis infection. Therapy with Ruxolitinib was interrupted due to possible immunsuppressive effects and the patient was treated with the standard antituberculosis regimen. After six months, the patient's symptoms had resolved and there was no lymphoadenopathy. In conclusion, it is important to assess the risk of tuberculosis activation before Ruxolitinib treatment. In addition, the diagnosis of tuberculosis using QuantiFERON-TB and PPD may be misleading in patients treated with Ruxolutinib.
原发性骨髓纤维化(PMF)是一种克隆性干细胞疾病,其特征为骨髓纤维化。芦可替尼是一种用于治疗PMF的JAK-1和JAK-2选择性抑制剂。其作用机制基于信号转导和细胞因子水平的降低,包括白细胞介素-6和肿瘤坏死因子α。与芦可替尼相关的感染风险增加鲜有报道。在此,我们描述一例接受芦可替尼治疗的女性患者发生结核感染复发的病例。治疗期间,她主诉盗汗、体重减轻及颈部肿块增大。切除肿块活检显示为坏死性肉芽肿性淋巴结炎。结核感染T细胞检测(QuantiFERON-TB)和结核菌素试验(PPD)均无法诊断结核感染。由于可能的免疫抑制作用,中断了芦可替尼治疗,患者接受标准抗结核方案治疗。六个月后,患者症状缓解,无淋巴结病。总之,在芦可替尼治疗前评估结核激活风险很重要。此外,对于接受芦可替尼治疗的患者,使用结核感染T细胞检测(QuantiFERON-TB)和结核菌素试验(PPD)诊断结核可能会产生误导。