Thrombotic thrombocytopenic purpura-hemolytic uremic syndrome in relapsing-remitting multiple sclerosis patients on high-dose interferon β

Author:

Larochelle Catherine12,Grand’maison François3,Bernier Gilles P2,Latour Mathieu4,Cailhier Jean-François5,Prat Alexandre12

Affiliation:

1. Neuroimmunology Research Laboratory, Centre de Recherche du Centre Hospitalier de l’Université de Montréal (CRCHUM), Canada

2. Department of Neurology, Université de Montréal, Canada

3. Department of Neurology, Université de Sherbrooke, Canada

4. Department of Pathology, Université de Montréal, Canada

5. Department of Medicine, Université de Montréal, Canada

Abstract

Three women aged 34–47 years old, on high dose interferon beta-1a for relapsing–remitting multiple sclerosis, were hospitalized between 2009–2012 for thrombotic thrombocytopenic purpura-hemolytic uremic syndrome. Patients sought medical attention for neurological symptoms including cephalalgia, blurred vision, confusion, focal deficits and seizures. All patients presented thrombocytopenia, hemolytic anemia and arterial hypertension. Despite plasma exchanges, corticosteroids and anti-CD20 treatments, all patients progressed towards severe renal insufficiency and one patient died of hemorrhagic shock. In this report we identify a rare but morbid complication of interferon beta-1a treatment associated with female gender, Caucasian background and low body mass index.

Publisher

SAGE Publications

Subject

Clinical Neurology,Neurology

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