Uppal S S, Pande I R, Kumar A, Kailash S, Sekharan N G, Adya C M, Malaviya A N
Department of Medicine, All India Institute of Medical Sciences, New Delhi.
Br J Rheumatol. 1995 May;34(5):429-34. doi: 10.1093/rheumatology/34.5.429.
The present study compared the clinical and laboratory picture, the disease course and outcome in 31 patients having adult onset Still's disease (AOSD) with 23 patients having juvenile onset Still's disease (JOSD). The median age at disease onset was 20 and 7 yr for AOSD and JOSD patients, respectively. On analysing and comparing our data on these two groups, no significant differences emerged except that adults had a significantly lower time interval from disease onset to remission as compared to juveniles. Upon comparison of data on our AOSD patients with that published from abroad, rash, adenopathy and sore throat were less frequent. No clinical or laboratory variables were found to predict the subsequent disease course and outcome in either group. The functional outcome was good in about 70% of both groups and mortality was low. It is concluded that the clinical picture and outcome in AOSD is similar to that of JOSD.
本研究比较了31例成人斯蒂尔病(AOSD)患者与23例青少年斯蒂尔病(JOSD)患者的临床和实验室检查结果、病程及预后。AOSD和JOSD患者发病时的中位年龄分别为20岁和7岁。在分析和比较这两组数据时,除成人从发病到缓解的时间间隔明显短于青少年外,未发现显著差异。将我们AOSD患者的数据与国外发表的数据进行比较时,皮疹、淋巴结病和咽痛的发生率较低。在两组中均未发现临床或实验室变量可预测随后的病程及预后。两组中约70%的患者功能预后良好,死亡率较低。结论是,AOSD的临床表现和预后与JOSD相似。