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
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.