Kuroda Takeshi, Takeuchi Hiroyuki, Nozawa Yukiko, Sato Hiroe, Nakatsue Takeshi, Wada Yoko, Moriyama Hiroshi, Nakano Masaaki, Narita Ichiei
Division of Clinical Nephrology and Rheumatology, Niigata University Graduate School of Medical and Dental Sciences, 1-757 Asahimachi-Dori, Chuoku, Niigata City, 951-8510, Japan.
Department of Respiratory Medicine and Infectious Diseases, Niigata University Graduate School of Medical and Dental Sciences, 1-757 Asahimachi-Dori, Chuoku, Niigata City, 951-8510, Japan.
BMC Res Notes. 2016 Apr 26;9:240. doi: 10.1186/s13104-016-2052-0.
Pneumocystis jirovecii pneumonia (PCP) is potentially fatal infectious complication in patients with rheumatoid arthritis (RA) during immunosuppressive therapy. Hospital survival due to human immunodeficiency virus-unrelated PCP reaches to 60%. The high mortality rate results from difficulties in establishing an early diagnosis, concurrent use of prophylactic drugs, possible bacterial coinfection. We herein report a case of PCP in RA patients who developed the architectural distortions of lung in spite of combined modality therapy.
A 73-year-old Japanese woman with RA was admitted with shortness of breath. Five weeks previously, she had been started on etanercept in addition to methotrexate (MTX). Chest computed tomography (CT) demonstrated diffuse ground glass opacities distributed throughout the bilateral middle to lower lung fields, and serum β-D-glucan was elevated. Bronchoalveolar lavage fluid revealed no P. jirovecii, but the organism was detected by polymerase chain reaction method. Trimethoprim/sulfamethoxazole was administered with methylprednisolone pulse therapy. However, the follow-up chest X-ray and chest CT demonstrated aggravation of the pneumonia with architectural distortions. Additional direct hemoperfusion with polymyxin B-immobilized fibers and intravenous cyclophosphamide therapy were insufficiently effective, and the patient died on day 25.
The architectural distortions of lung should be considered as a cause of death of PCP. For this reason, a high suspicion of this infectious complication must be kept in mind in order to establish an early diagnosis and treatment in patients with RA managed with MTX and biologics.
耶氏肺孢子菌肺炎(PCP)是类风湿关节炎(RA)患者在免疫抑制治疗期间潜在的致命性感染并发症。与人类免疫缺陷病毒无关的PCP患者的医院生存率可达60%。高死亡率是由于早期诊断困难、预防性药物的同时使用以及可能的细菌合并感染。我们在此报告一例RA患者发生PCP,尽管采用了联合治疗方式,但仍出现了肺部结构扭曲。
一名73岁的日本女性RA患者因呼吸急促入院。五周前,她除了服用甲氨蝶呤(MTX)外,还开始使用依那西普。胸部计算机断层扫描(CT)显示双侧中下部肺野弥漫性磨玻璃影,血清β-D-葡聚糖升高。支气管肺泡灌洗未发现耶氏肺孢子菌,但通过聚合酶链反应方法检测到了该病原体。给予甲氧苄啶/磺胺甲恶唑联合甲基强的松龙脉冲治疗。然而,后续的胸部X线和胸部CT显示肺炎加重并伴有结构扭曲。额外的多粘菌素B固定纤维直接血液灌流和静脉环磷酰胺治疗效果不佳,患者于第25天死亡。
肺部结构扭曲应被视为PCP的死亡原因。因此,对于接受MTX和生物制剂治疗的RA患者,为了早期诊断和治疗,必须高度怀疑这种感染并发症。