Eculizumab in a child with atypical haemolytic uraemic syndrome and haemophagocytic lymphohistiocytosis triggered by cytomegalovirus infection

We present the case of a 21-month-old girl with two rare and life-threatening conditions, atypical haemolytic uraemic syndrome (aHUS) and haemophagocytic lymphohistiocytosis (HLH), triggered by a cytomegalovirus (CMV) infection. Soon after admission, the girl became anuric and required continuous ve...

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Detalhes bibliográficos
Autores: Fraga Rodriguez, Gloria Maria|||0000-0002-7682-1396, Brió Sanagustín, Sonia|||0000-0002-1520-4618, Turon Viñas, Eulalia|||0000-0001-6171-0282, Dixon, Bradley P.., Carreras, Eduardo
Tipo de documento: artigo
Data de publicação:2017
País:España
Recursos:Universitat Autònoma de Barcelona
Repositório:Dipòsit Digital de Documents de la UAB
Idioma:inglês
OAI Identifier:oai:ddd.uab.cat:186218
Acesso em linha:https://ddd.uab.cat/record/186218
https://dx.doi.org/urn:doi:10.1136/bcr-2016-219065
Access Level:Acceso aberto
Palavra-chave:Haematology (drugs and medicines)
Paediatrics (drugs and medicines)
Renal system
Haematology (incl blood transfusion)
Descrição
Resumo:We present the case of a 21-month-old girl with two rare and life-threatening conditions, atypical haemolytic uraemic syndrome (aHUS) and haemophagocytic lymphohistiocytosis (HLH), triggered by a cytomegalovirus (CMV) infection. Soon after admission, the girl became anuric and required continuous venovenous haemodiafiltration. Initial treatments included methylprednisolone, fibrinogen and plasma infusion (for HLH), plasmapheresis (for thrombotic microangiopathy), immunoglobulins (for inflammation), ganciclovir (for CMV infection) and the antibiotic cefotaxime. On day 5, eculizumab (600 mg) was given for aHUS, with rapid improvement in haematological and nephrological parameters. Despite a subsequent isolated episode of right heart thrombosis that resolved with heparin treatment, the patient showed a favourable response to eculizumab (300 mg/15 days), with improved renal function, normal haematological values, and no treatment complications. In conclusion, eculizumab effectively treated aHUS in this case despite a comorbid immunological disease.