IgA nephropathy and atypical hemolytic uremic syndrome: a case series and a literature review.
Lucio ManentiGiovanni Maria RossiIsabella PisaniMicaela GentileFrancesco FontanaFrancesco Paolo PilatoMarco DelsanteFederico RiccoRenzo MignaniCaterina MeleElena BresinEnrico FiaccadoriPublished in: Journal of nephrology (2021)
Our case series and literature review show that the onset of either aHUS or renal TMA in the course of IgAN are associated with very poor renal outcome. Activation of the alternative pathway revealed by consumption of serum C3 seems to play a major role. Our hypothesis is that the presence of a predisposing factor (e.g. dysregualtion of complement alternative pathway and/or other intrarenal precipitating factors) might be at the heart of aHUS-IgAN pathophysiology.
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