R. Cevallos et al., RAPIDLY PROGRESSIVE GLOMERULONEPHRITIS DU RING MACROSCOPIC POLYARTERITIS-NODOSA - 7 CASES, Annales de medecine interne, 144(5), 1993, pp. 311-313
Rapidly progressive glomerulonephritis (RPGN) is rarely associated wit
h macroscopic polyarteritis nodosa (pAN), as seen in this series of 7
out of 235 patients. The clinical symptoms of PAN were as follows : my
algias 6 ; fever 1 ; arthralgias and mononeuropathy multiplex 5 ; cuta
neous vasculitis 3 ; arterial hypertension 4, 3 of which malignant. Th
e mean protein was 2.7 g/24 h ; creatininemia 458 muM/l ; microscopic
hematuria was present in 4 of the 7 patients only 1 patient was anuric
. Markers of hepatitis B virus were absent in all cases. Arteriography
revealed microaneurysms and renal infarcts in 6 patients and distal a
rterial stenosis in one. Renal biopsies from all 7 patients demonstrat
ed extracapillary glomerulonephritis, which was associated with tubulo
interstitial fibrosis in one. Necrotizing vasculitis lesions were asso
ciated in 5 cases. Immunofluorescence was positive in 5 cases. The ass
ociation of RPGN and PAN exists and may be underestimated due to the l
ack of systematic angiographic examinations during RPGN and renal biop
sies in PAN patients with renal involvement.