2021
DOI: 10.1177/1352458521993070
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Hemophagocytic lymphohistiocytosis associated with ocrelizumab treatment in a patient with multiple sclerosis

Abstract: Background: Hemophagocytic lymphohistiocytosis (HLH) is a rarely recognized hyperinflammatory condition of high death risk. Objective: The objective was to describe a case of HLH in a patient with multiple sclerosis (MS) treated with ocrelizumab Methods: Clinical observation, laboratory testing, and use of HLH-2004 criteria for HLH diagnosis. Results: A 32-year-old Caucasian female developed HLH during ocrelizumab treatment. She met six of the eight HLH criteria including fever, splenomegaly, cytopenia, hypert… Show more

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Cited by 4 publications
(1 citation statement)
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“…Moreover, due to the inclusion of a highly selected population, adverse events might be also underestimated in pivotal trials [13,14]. Since the positioning of ocrelizumab is still not well established within the therapeutic algorithm for MS, it is crucial to provide clinicians with relevant information on prognostic and predictive factors that can help assess the benefit-risk ratio.…”
Section: Introductionmentioning
confidence: 99%
“…Moreover, due to the inclusion of a highly selected population, adverse events might be also underestimated in pivotal trials [13,14]. Since the positioning of ocrelizumab is still not well established within the therapeutic algorithm for MS, it is crucial to provide clinicians with relevant information on prognostic and predictive factors that can help assess the benefit-risk ratio.…”
Section: Introductionmentioning
confidence: 99%