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Drug-induced thrombocytopenia secondary to natalizumab treatment

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Summary 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.
Title: Drug-induced thrombocytopenia secondary to natalizumab treatment
Description:
Summary 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.

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