Kim Mi-Yeong, Sohn Kyoung-Hee, Song Woo-Jung, Park Heung-Woo, Cho Sang-Heon, Min Kyung-Up, Kang Hye-Ryun
Department of Internal Medicine, Inje University Busan Paik Hospital, Busan, Korea.
Department of Internal Medicine, Seoul National University Hospital, Seoul, Korea. ; Institute of Allergy and Clinical Immunology, Seoul National University Medical Research Center, Seoul, Korea.
Korean J Intern Med. 2014 Jan;29(1):85-95. doi: 10.3904/kjim.2014.29.1.85. Epub 2014 Jan 2.
BACKGROUND/AIMS: Churg-Strauss syndrome (CSS) is a rare systemic necrotizing small-vessel vasculitis, with accompanying bronchial asthma, eosinophilia, and eosinophilic infiltration of various tissues. The purposes of our study were to characterize the clinical features of CSS and to identify factors associated with CSS prognosis in Koreans.
Medical records were reviewed retrospectively for all physician-diagnosed CSS patients in the Seoul National University Hospital between January 1990 and March 2011.
Data from 52 CSS patients were analyzed. The respiratory tract was the most commonly involved organ (90.4%). Renal involvement was less frequent in antineutrophilic cytoplasmic antibody (ANCA)(-) patients than in ANCA(+) patients (p = 0.048). Clinical remission occurred in 95.3% of patients, but 16.3% of them relapsed. Patients who maintained remission for more than 6 months were relatively older (median, 51 years) at diagnosis (p = 0.004), had been diagnosed in earlier stages (p = 0.027), showed more frequent respiratory involvement (p = 0.024) and generalized symptoms (p = 0.039), and showed less frequent cutaneous involvement (p = 0.030) than those who did not achieve persistent (> 6 months) remission. Patients who achieved persistent remission also showed higher C-reactive protein (CRP) levels (p = 0.031) than those who did not.
ANCA(-) CSS patients showed less frequent renal involvement. Characteristics of good responders were older age, diagnosis at earlier stages, less cutaneous involvement, more respiratory involvement, high CRP values, and more generalized symptoms.
背景/目的:变应性肉芽肿性血管炎(CSS)是一种罕见的系统性坏死性小血管炎,伴有支气管哮喘、嗜酸性粒细胞增多以及各种组织的嗜酸性粒细胞浸润。我们研究的目的是描述韩国CSS患者的临床特征,并确定与CSS预后相关的因素。
回顾性分析1990年1月至2011年3月期间首尔国立大学医院所有经医生诊断的CSS患者的病历。
分析了52例CSS患者的数据。呼吸道是最常受累的器官(90.4%)。抗中性粒细胞胞浆抗体(ANCA)阴性患者的肾脏受累频率低于ANCA阳性患者(p = 0.048)。95.3%的患者实现了临床缓解,但其中16.3%复发。缓解持续超过6个月的患者在诊断时年龄相对较大(中位数为51岁)(p = 0.004),诊断时处于早期阶段(p = 0.027),呼吸道受累更频繁(p = 0.024),全身症状更常见(p = 0.039),皮肤受累频率低于未实现持续(>6个月)缓解的患者(p = 0.030)。实现持续缓解的患者的C反应蛋白(CRP)水平也高于未实现持续缓解的患者(p = 0.031)。
ANCA阴性的CSS患者肾脏受累频率较低。缓解良好者的特征为年龄较大、早期诊断、皮肤受累较少、呼吸道受累较多、CRP值高以及全身症状较多。