Caroleo Benedetto, Migliore Alberto, Cione Erika, Zampogna Stefania, Perticone Francesco, Sarro Giovambattista De, Gallelli Luca
Department of Medical and Surgical Science, School of Medicine, University of Catanzaro and Elderly Disease Operative Unit Mater Domini Hospital, Catanzaro, Italy.
Department of Rheumatology San Pietro Hospital, Rome, Italy.
Curr Drug Saf. 2019;14(2):147-150. doi: 10.2174/1574886314666190114124625.
Either direct or indirect tumor necrosis factor (TNF)-alpha blockers are usually used to treat psoriatic arthritis (PA), but their use can increase susceptibility to infectious diseases.
We report a rare case of double skin-knee wound and lung non-tubercular infection in a patient with PA under TNF-alpha blockers therapy. About 1 year after the beginning of adalimumab, a 48-year-old smoker suffering of PA was hospitalized for the skin-knee wound.
Clinical evaluation and biochemical markers excluded the presence of a systemic disease, and a skin infection sustained by leishmaniasis probably related to adalimumab was diagnosed (Naranjo score: 6). Adalimumab was discontinued and oral treatment with apremilast and topical treatment with meglumine antimoniate was started with a complete remission of skin wound in 2 weeks. About 7 months later when the patient was under apremilast treatment, he presented to our observation for dyspnea, cough and fever. High-Resolution Computer Tomography (HRCT) chest highlighted alveolar involvement with centrilobular small nodules, branching linear and nodular opacities. Microbiological culture of both broncho-alveolar lavage fluid and sputum documented an infection sustained by nontuberculous mycobacteria. Even if apremilast treatment probably-induced lung infection, we can't exclude that it worsened a clinical condition induced by adalimumab. Apremilast was stopped and an empirical antitubercular treatment was started. Patient's breathlessness and cough improved as confirmed also by HRCT chest.
This case highlights the importance to consider the possibility to develop leishmaniasis and/or non-tubercular mycobacterial infection in patients treated with TNF-alpha inhibitors.
直接或间接的肿瘤坏死因子(TNF)-α阻滞剂通常用于治疗银屑病关节炎(PA),但其使用会增加对传染病的易感性。
我们报告了1例在接受TNF-α阻滞剂治疗的PA患者中出现双膝皮肤伤口和肺部非结核感染的罕见病例。在开始使用阿达木单抗约1年后,一名患有PA的48岁吸烟者因双膝皮肤伤口住院。
临床评估和生化指标排除了全身性疾病的存在,诊断为可能与阿达木单抗相关的利什曼病引起的皮肤感染(纳朗霍评分:6分)。停用阿达木单抗,开始使用阿普斯特口服治疗和葡甲胺锑酸盐局部治疗,2周内皮肤伤口完全愈合。约7个月后,患者在接受阿普斯特治疗时,因呼吸困难、咳嗽和发热前来就诊。胸部高分辨率计算机断层扫描(HRCT)显示肺泡受累,伴有小叶中心小结节、分支状线性和结节状混浊。支气管肺泡灌洗液和痰液的微生物培养证实为非结核分枝杆菌感染。即使阿普斯特治疗可能诱发肺部感染,我们也不能排除它加重了阿达木单抗引起的临床状况。停用阿普斯特并开始经验性抗结核治疗。患者的呼吸急促和咳嗽症状有所改善,胸部HRCT也证实了这一点。
该病例突出了在使用TNF-α抑制剂治疗的患者中考虑发生利什曼病和/或非结核分枝杆菌感染可能性的重要性。