Zhang Q, Zhou H Q, Li Y H, Guo J, Xu P H, Lu M H, Liu X L, Wang L, Li S G
Department of Rheumatology, the First Affiliated Hospital of PLA General Hospital, Beijing 100048, China.
Zhonghua Yi Xue Za Zhi. 2016 Jul 19;96(27):2146-9. doi: 10.3760/cma.j.issn.0376-2491.2016.27.007.
To investigate the clinical features of patients with antineutrophil cytoplasmic antibody (ANCA) associated vasculitis (AAV), and to explore the disease activity of AAV patients and the relationship with prognosis.
The clinical data of 46 cases of AAV patients in the First Affiliated Hospital of PLA General Hospital were analyzed retrospectively.The clinical and laboratory features of each clinical subtype were compared.The disease activity of AAV and the relationship between disease activity and prognosis were evaluated.
Among the 46 patients with AAV, 24 were male, and 22 were female, with the average age of 56±18.Among the subtypes of AAV, the number of granulomatosis with polyangiitis (GPA), microscopic polyangiitis (MPA), and eosinophilic granulomatosis with polyangiitis (EGPA) were 22, 17 and 4 respectively, while the positive rate of ANCA are 72.7%, 88.2% and 50.0% respectively.For GPA, the results of ANCA were mainly C-ANCA or ANCA directed toward proteinase-3 (PR3), and for MPA, the results of ANCA were mainly P-ANCA or ANCA directed toward myeloperoxidase (MPO). Upper and lower respiratory disease, renal involvement and non-deformity arthropathy were the common clinical manifestations of all primary AAV subtypes.Epistaxis, nasal blood scab, saddle nose, pulmonary nodule and intrapulmonary cavities were the characteristic manifestations of GPA, while rapid progress of renal failure was prominent in MPA.Whatever their ANCA results, there were no significant differences between each other as to system-organ involvements and laboratory indexes.Seven patients (15.2%) died during hospitalization or in follow-up visits.Serious involvements of heart, lung, kidney, and complicated with infections were the main risk factors of death in AAV patients.
Upper and lower respiratory involvements and kidney diseases are the primary manifestations of AAV patients.ANCA results are irrelevant with disease activity and system-organ involvements.Serious involvements of heart, lung, kidney, and complicated with infections are the main risk factors of death in AAV patients.
探讨抗中性粒细胞胞浆抗体(ANCA)相关性血管炎(AAV)患者的临床特征,分析AAV患者的疾病活动度及其与预后的关系。
回顾性分析解放军总医院第一附属医院46例AAV患者的临床资料,比较各临床亚型的临床及实验室特征,评估AAV的疾病活动度以及疾病活动度与预后的关系。
46例AAV患者中,男性24例,女性22例,平均年龄56±18岁。AAV各亚型中,肉芽肿性多血管炎(GPA)22例、显微镜下多血管炎(MPA)17例、嗜酸性肉芽肿性多血管炎(EGPA)4例,ANCA阳性率分别为72.7%、88.2%、50.0%。GPA患者ANCA结果以C-ANCA或抗蛋白酶3(PR3)型ANCA为主,MPA患者ANCA结果以P-ANCA或抗髓过氧化物酶(MPO)型ANCA为主。上、下呼吸道病变、肾脏受累及非畸形性关节病是所有原发性AAV亚型的常见临床表现。鼻出血、鼻痂、鞍鼻、肺结节及肺内空洞是GPA的特征性表现,而MPA以肾衰竭进展迅速为突出表现。无论ANCA结果如何,各系统器官受累情况及实验室指标相互间差异均无统计学意义。7例患者(15.2%)在住院期间或随访中死亡。心脏、肺、肾脏的严重受累及合并感染是AAV患者死亡的主要危险因素。
上、下呼吸道受累及肾脏病变是AAV患者的主要表现。ANCA结果与疾病活动度及系统器官受累情况无关。心脏、肺、肾脏的严重受累及合并感染是AAV患者死亡的主要危险因素。