| Literature DB >> 32081100 |
Alice Horisberger1, Vasiliki Pantazou2, Géraldine Cuendet3, Camillo Ribi1, Vincent Dunet4, Marie Théaudin2.
Abstract
Alemtuzumab is highly effective in relapsing remitting multiple sclerosis (RRMS), but autoimmune adverse events are of concern. In contrast to rare cases of immune-mediated cutaneous vasculitis, systemic vasculitis after alemtuzumab has not yet been described. We report the case of a 29-year-old man with RRMS who developed fever, auricular chondritis, cutaneous vasculitis and life-threatening diffuse alveolar haemorrhage, 12 months after alemtuzumab. Antibodies to myeloperoxidase appeared 9 months after alemtuzumab and were extremely high at the time of vasculitis. Outcome was favourable after glucocorticoids, plasma exchanges and rituximab. Thus, alemtuzumab may induce life-threatening vasculitis in patients treated for RRMS.Entities:
Keywords: Alemtuzumab; multiple sclerosis
Year: 2020 PMID: 32081100 DOI: 10.1177/1352458519895449
Source DB: PubMed Journal: Mult Scler ISSN: 1352-4585 Impact factor: 6.312