Uppal Sukhbir Singh, Al-Mutairi Moudhi, Hayat Sawsan, Abraham Mini, Malaviya Anand
Rheumatology Division, Department of Medicine, Mubarak Al-Kabeer Hospital, Jabriya, Kuwait.
Clin Rheumatol. 2007 Jul;26(7):1055-60. doi: 10.1007/s10067-006-0440-x. Epub 2006 Nov 4.
This study aims to report on the clinical and laboratory picture and the disease course and outcome in patients having adult onset Still's disease (AOSD), to briefly review existing literature on the subject, and to compare our findings with those previously reported. Results are reported for 28 patients with AOSD satisfying the preliminary criteria of Yamaguchi et al. seen in a teaching hospital over the last 10 years. A high percent of the patients with AOSD were women. The mean (+SD) age at disease onset was 27.8 (+8.4) years. We found fever in 100%, rash in 85%, arthritis in 64%, lymphadenopathy in 60%, splenomegaly in 57%, hepatomegaly in 35%, pleural effusion in 17.9%, and pericardial effusion in 3.6% of our patients. Leukocytosis was present in 96% of the patients, a normochromic, normocytic anemia in 54%, and an elevated erythrocyte sedimentation rate (ESR) in all. Serum ferritin levels were raised in 89% of the patients. The mean follow-up of the patients was 3.72 + 2.46 years. The mean delay in diagnosis was 7.32 + 18.0 months. The mean time to enter remission was 9.7 months. Self-limited, intermittent, and chronic disease course was seen in 14.3, 57.1, and 28.6% of patients, respectively. The outcome was good in about 89% of patients, and mortality was nil. No particular clinical or laboratory variable was found to predict the subsequent disease course and outcome in our patients. On comparing our data with important previous series, we found a higher percentage of women and of patients presenting in the age group 16-35 years, a lower frequency of arthritis and pericardial effusion, and some other notable differences. Importantly, the disease course was benign, probably as an outcome of heightened awareness and less diagnostic delay than in the past, allowing for early, aggressive, and appropriate treatment. It is concluded that AOSD is now a relatively benign disease if diagnosed early and treated appropriately.
本研究旨在报告成年斯蒂尔病(AOSD)患者的临床和实验室检查情况、疾病进程及转归,简要回顾该主题的现有文献,并将我们的研究结果与先前报道的结果进行比较。报告了过去10年在一家教学医院中符合山口等人初步标准的28例AOSD患者的结果。AOSD患者中女性占比很高。疾病发作时的平均(±标准差)年龄为27.8(±8.4)岁。我们发现,100%的患者有发热,85%有皮疹,64%有关节炎,60%有淋巴结病,57%有脾肿大,35%有肝肿大,17.9%有胸腔积液,3.6%有心包积液。96%的患者有白细胞增多,54%有正色素、正细胞性贫血,所有患者红细胞沉降率(ESR)均升高。89%的患者血清铁蛋白水平升高。患者的平均随访时间为3.72±2.46年。诊断的平均延迟时间为7.32±18.0个月。进入缓解期的平均时间为9.7个月。分别有14.3%、57.1%和28.6%的患者出现自限性、间歇性和慢性病程。约89%的患者转归良好,无死亡病例。在我们的患者中,未发现特定的临床或实验室变量可预测后续疾病进程及转归。将我们的数据与之前重要系列研究进行比较时,我们发现女性以及16 - 35岁年龄组患者的比例更高,关节炎和心包积液的发生率更低,还有一些其他显著差异。重要的是,疾病进程呈良性,这可能是由于现在比过去意识提高且诊断延迟减少,从而能够进行早期、积极且恰当的治疗。结论是,如果早期诊断并适当治疗,AOSD现在是一种相对良性的疾病。