THE SPECTRUM OF RENAL-DISEASE ASSOCIATED WITH MICROSCOPIC POLYANGIITIS AND CLASSIC POLYARTERITIS-NODOSA IN KUWAIT

Citation
K. Elreshaid et al., THE SPECTRUM OF RENAL-DISEASE ASSOCIATED WITH MICROSCOPIC POLYANGIITIS AND CLASSIC POLYARTERITIS-NODOSA IN KUWAIT, Nephrology, dialysis, transplantation, 12(9), 1997, pp. 1874-1882
Citations number
22
Categorie Soggetti
Urology & Nephrology",Transplantation
ISSN journal
09310509
Volume
12
Issue
9
Year of publication
1997
Pages
1874 - 1882
Database
ISI
SICI code
0931-0509(1997)12:9<1874:TSORAW>2.0.ZU;2-6
Abstract
Background. This study was conducted to examine prospectively the epid emiological profile of renal disease associated with microscopic polya ngiitis (MPA) and classic polyarteritis nodosa (classic PAN) in Kuwait and its clinicopathological correlation. Methods. Between 1 January 1 993 and 31 December 1996, all patients referred to Al-Amiri renal cent re were subjected to renal biopsy and/or arteriography if they manifes ted systemic manifestations of vasculitis or had rapid or unexplained renal failure with or without proteinuria. Patients who fulfilled the criteria of MPA and classic PAN, according to the Chapel Hill Consensu s Conference (CHCC), were included in the study. Results. Over those 4 years, 47 patients were diagnosed as having such vasculitides, 22 of whom were Kuwaiti nationals. This gave an average annual incidence of 45 cases/million adult Kuwaiti nationals (95% CI, 27-64). Histological examination revealed necrotizing glomerulonephritis (GN) in 11 patien ts and crescentic GN in 13, while isolated small- and/or medium-sized- arteritis were evident in six more patients. In 10 of the remaining pa tients, bands of fibrosis alternating with healthy renal tissue were s een and on arteriography non-atherosclerotic stenoses, infarctions, an d/or microaneurysms were evident. The remaining seven patients were di agnosed by arteriography alone, five of whom had bilateral small kidne ys. Constitutional manifestations of vasculitis were present in 32 pat ients (68%) and multisystem involvement in 19 (40%). ANCA levels were high in 24 (55%) of the 44 patients tested and seropositivity, as an a ntimyeloperoxidase, was a constant finding. Only six patients presente d with rapidly progressive renal failure, while 31 presented with chro nic renal disease, 18 of whom had protein excretion in excess of 2 g/d ay. Conclusions. These findings emphasize the limited role of clinical assessment in establishing a definite diagnosis of renal vasculitis a nd put in question its value in retrospective analysis of causes of ES RD in different populations.