Vanheule B A, Carswell F
Eur J Pediatr. 1983 Mar;140(1):66-8. doi: 10.1007/BF00661910.
A case is reported of lupus syndrome in a 13-year-old girl with ulcerative colitis treated with sulphasalazine. She had antibodies to nuclear factor and double-stranded DNA. The clinical pattern resembled drug-induced systemic lupus erythematosus and has resolved since her sulphasalazine was discontinued. Sulphasalazine-induced lupus syndrome has never been reported in a child. The history illustrates the role of sulphasalazine in the development of this syndrome.
报告了一例13岁患有溃疡性结肠炎且正在接受柳氮磺胺吡啶治疗的女孩出现狼疮综合征的病例。她有抗核因子和双链DNA抗体。临床症状类似于药物性系统性红斑狼疮,自停用柳氮磺胺吡啶后症状已缓解。柳氮磺胺吡啶诱发的狼疮综合征从未在儿童中报道过。该病例说明了柳氮磺胺吡啶在这种综合征发生过程中的作用。