Kirkland G S, Savige J, Wilson D, Heale W, Sinclair R A, Hope R N
University Department of Medicine, Austin and Repatriation Medical Centre, Heidelberg, Victoria, Australia.
Clin Nephrol. 1997 Mar;47(3):176-80.
Microscopic polyarteritis may involve medium-sized and small blood vessels as well as arterioles, venules and capillaries. We have compared the clinical and laboratory features in patients with microscopic polyarteritis and medium vessel involvement, with the features found in patients with polyarteritis nodosa affecting medium vessels alone. In a 9-year period, 21 patients presented to our hospital with a form of polyarteritis. Seven had microscopic polyarteritis demonstrated histologically (6/7, 86%) and associated with dysmorphic urinary red cells (7/7, 100%), as well as medium vessel vasculitis demonstrated histologically (7/7) or by angiography (1/7, 14%). Five patients had polyarteritis nodosa with medium vessel vasculitis demonstrated histologically (3/5, 60%) or by angiography (2/5, 40%); and no evidence of a glomerular vasculitis on biopsy (2/7, 29%) or in the urinary sediment (0/7, 0%). The remaining 9 patients had microscopic polyarteritis but medium vessel involvement was not excluded by angiography. All patients with microscopic polyarteritis and medium vessel involvement had glomerular hematuria (> 100,000 glomerular RBC/ml), proteinuria > 0.5 g/24 hours), and an elevated serum creatinine (0.166 to 0.811 mmol/l). Other symptoms included fever (6/7, 86%), night sweats (5/7, 71%), gastrointestinal bleeding (4/7, 57%), proximal myopathy (3/7, 43%) and peripheral neuropathy (3/7, 43%). One patient (1/7, 14%) had hypertension. Anemia (6/7, 86%), a raised ESR (6/7, 86%), thrombocytosis (6/7, 86%), hypoalbuminemia (6/7, 86%) and abnormal liver function tests (6/7, 86%) were common. Two patients (29%) had an eosinophilia. All 5 individuals who were tested for ANCA were positive (2cANCA, 2pANCA and one pattern not described). In contrast, in patients with polyarteritis nodosa and medium vessel involvement alone, an elevated ESR was common (4/5, 80%) but fever (1/5, 20%), night sweats (0/5, 0%), proximal myopathy (1/5, 20%) and peripheral neuropathy (1/5, 20%) were seen infrequently; hypertension (1/5, 20%) and eosinophilia (1/5, 20%) were also uncommon; and ANCA were not demonstrated (0/3, 0%). Medium-sized vessel involvement is common in patients with microscopic polyarteristis, and these patients are more likely to have renal involvement and systemic symptoms, and be ANCA-positive, than patients with polyarteritis nodosa alone. Gastrointestinal symptoms are often seen in both groups.
显微镜下多动脉炎可累及中、小血管以及微动脉、微静脉和毛细血管。我们比较了显微镜下多动脉炎伴中血管受累患者的临床和实验室特征,以及仅累及中血管的结节性多动脉炎患者的特征。在9年期间,21例患者因某种形式的多动脉炎前来我院就诊。7例经组织学证实为显微镜下多动脉炎(6/7,86%),伴有异形尿红细胞(7/7,100%),以及经组织学(7/7)或血管造影(1/7,14%)证实的中血管血管炎。5例患者经组织学(3/5,60%)或血管造影(2/5,40%)证实为结节性多动脉炎伴中血管血管炎;活检(2/7,29%)或尿沉渣检查(0/7,0%)未发现肾小球血管炎证据。其余9例患者为显微镜下多动脉炎,但血管造影未排除中血管受累。所有显微镜下多动脉炎伴中血管受累患者均有肾小球性血尿(>100,000个肾小球红细胞/ml)、蛋白尿>0.5 g/24小时)以及血清肌酐升高(0.166至0.811 mmol/l)。其他症状包括发热(6/7,86%)、盗汗(5/7,71%)、胃肠道出血(4/7,57%)、近端肌病(3/7,43%)和周围神经病变(3/7,43%)。1例患者(1/7,14%)有高血压。贫血(6/7,86%)、血沉升高(6/7,86%)、血小板增多(6/7,86%)、低白蛋白血症(6/7,86%)和肝功能检查异常(6/7,86%)较为常见。2例患者(29%)有嗜酸性粒细胞增多。所有检测ANCA的5例患者均为阳性(2例cANCA、2例pANCA和1例未描述的类型)。相比之下,仅累及中血管的结节性多动脉炎患者中,血沉升高较为常见(4/5,80%),但发热(1/5,20%)、盗汗(0/5,0%)、近端肌病(1/5,20%)和周围神经病变(1/5,20%)少见;高血压((1/5,20%)和嗜酸性粒细胞增多(1/5,20%)也不常见;且未检测到ANCA(0/3,0%)。中血管受累在显微镜下多动脉炎患者中很常见,与仅患结节性多动脉炎的患者相比,这些患者更易出现肾脏受累和全身症状,且ANCA呈阳性。两组患者均常出现胃肠道症状。