Rapidly progressive glomerulonephritis in a boy with hypocomplementaemic urticarial vasculitis
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Published on: September 20, 2018
M Renard1, C Wouters, W Proesmans
1University Hospital, Department of Paediatrics, Leuven, Belgium.
Unlabelled:
The present paper reports the fourth case of hypocomplementaemic urticarial vasculitis in a child. We describe a boy who, after many years of arthritis, urticaria, eye inflammation and hypocomplementaemia, developed rapidly progressive glomerulonephritis which was completely reversed by immunosuppressive therapy.
Conclusion:
Only three paediatric patients with hypocomplementaemic urticarial vasculitis have been described. Severe renal involvement was reversible with early appropriate treatment.
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