| Literature DB >> 24879724 |
David Cachia1, Saef Izzy2, Idanis Berriosmorales3, Carolina Ionete3.
Abstract
A 52-year-old woman with a 10-year history of relapsing-remitting multiple sclerosis (RRMS) was started on natalizumab after she developed side effects for interferon β-1a and glatiramer acetate. The patient presented with acute severe infusion reaction after the third treatment with natalizumab, developing whole-body purpura. Laboratory testing revealed progressive worsening thrombocytopenia up to 3 weeks following natalizumab discontinuation. Platelet antibodies to platelet-specific antigen as well as antibodies against natalizumab were positive. Bone marrow biopsy was negative. The patient was diagnosed with drug-induced immune thrombocytopenia (DITP) as a rare case of natalizumab side effect which was treated with intravenous methylprednisolone followed by rituximab with successful resolution of thrombocytopenia. The patient had a stable course of RRMS with no relapses and no brain MRI changes at 2 years after initiation of rituximab. 2014 BMJ Publishing Group Ltd.Entities:
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Year: 2014 PMID: 24879724 PMCID: PMC4039923 DOI: 10.1136/bcr-2013-203313
Source DB: PubMed Journal: BMJ Case Rep ISSN: 1757-790X