Fleischmann R M
Metroplex Clinical Research Center and University of Texas Southwestern Medical Center, Dallas, TX 75231, USA.
Arthritis Rheum. 2009 Nov;60(11):3225-8. doi: 10.1002/art.24906.
Progressive multifocal leukoencephalopathy (PML) is a rare brain disease caused by reactivation of the JC virus. Herein, a case of PML in association with rituximab treatment in a patient with chronic rheumatoid arthritis (RA) and Sjögren's syndrome is described. The patient received 4 courses of rituximab (2 1,000-mg infusions administered 2 weeks apart) over a period of approximately 40 months, during a phase III trial and safety extension study. PML was diagnosed approximately 18 months after the last rituximab course, and the patient died 1 month later. Determination of the cause of PML was confounded by the fact that the patient had developed oropharyngeal cancer, which was treated with chemoradiotherapy, 9 months prior to the development of PML. Although there was no direct evidence that linked rituximab to the development of PML, this case highlights the need to consider a diagnosis of PML in patients with RA who have been treated with rituximab and who subsequently develop new neurologic symptoms.
进行性多灶性白质脑病(PML)是一种由JC病毒重新激活引起的罕见脑部疾病。在此,描述了一例在患有慢性类风湿性关节炎(RA)和干燥综合征的患者中与利妥昔单抗治疗相关的PML病例。在一项III期试验和安全性扩展研究期间,该患者在约40个月的时间内接受了4个疗程的利妥昔单抗治疗(每次输注1000mg,间隔2周给药2次)。PML在最后一个利妥昔单抗疗程后约18个月被诊断出来,患者在1个月后死亡。由于患者在PML发生前9个月已患口咽癌并接受了放化疗,PML病因的确定受到了干扰。尽管没有直接证据将利妥昔单抗与PML的发生联系起来,但该病例凸显了对于接受利妥昔单抗治疗且随后出现新的神经系统症状的RA患者,需要考虑PML诊断的必要性。