Résumé
Introduction. The management of diarrhea-associated hemolytic and uremic syndrome (D+ HUS) with severe acute neurological involvement continues to be debated. We report on 2 cases and discuss the treatment.
Case report 1. A 2.5-year-old girl presented with generalized seizures during gastroenteritis. Blood tests revealed features of HUS and a pyramidal syndrome was found on physical examination. Brain MRI, 24 h after admission, showed lesions in the periventricular and subcortical area. She was started on peritoneal dialysis (PD) and daily plasma exchanges (PE) for 10 days. Her neurological condition improved quickly as well as the findings of the second brain MRI performed after PE. One year later she had no apparent neurological or renal sequelae.
Case report 2. A 2.5-year-old boy presented with generalized seizures during gastroenteritis for 3 days, leading to a diagnosis of H US. He also had a severe pyramidal syndrome with spastic tetraparesis and aphasia. Brain MRI, 48 h after admission, revealed severe bilateral and symmetric lesions involving the thalami, internal and external capsules, lenticular nuclei, and brainstem. He was started on PD and daily PE for 10 days. Brain MRI performed after PE was unchanged. Clinically, his neurological condition improved slowly with regression of spastic tetraparesis and progressive recovery of motor skills.. Nine months later, his renal function is normal but he is still having intensive physiotherapy.
Discussion. Both children have received similar management including 10 PEs started within 48 h after the diagnosis of D+ HUS with severe neurological involvement, but their neurological outcome appeared to be signicantly different. There is no clear proof in the literature concerning the effects of PE in such patients, even when performed very early. Eculizumab, an antibody that inhibits complement factor 5a and the formation of the membrane attack complex, has recently been used in such cases and seems to provide a more specific therapeutic action. Control studies are needed to specify its use in this disease. (C) 2011 Elsevier. Masson SAS. All rights reserved.