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An unforeseen reality: Hemophagocytic lymphohistiocytosis following alemtuzumab treatment for a multiple sclerosis [Elektronski vir]Ošep, Anka ...Alemtuzumab is a humanized monoclonal antibody indicated for treatment of highly active relapsing-remitting multiple sclerosis (HA-RRMS). It binds to CD52 antigen and produces a rapid and prolonged ... lymphocyte depletion followed by a different pattern of T and B cell repopulation. Among others, its adverse events are autoimmune diseases.In this article, we present a patient with HA-RRMS, who was subsequently treated with alemtuzumab and afterwards developed hemophagocytic lymphohistiocytosis (HLH). Albeit rarely, HLH can be triggered by alemtuzumab treatment.HLH can favourably respond to prompt immunosuppressant therapy.Multidisciplinary approach by a team consisting of a neurology, hematology and rheumatology specialist is needed to treat this potentially lethal condition.Source: Clinical neurology and neurosurgery. - ISSN 1872-6968 (Vol. 228, May, 2023, 107675)Type of material - e-article ; adult, seriousPublish date - 2023Language - englishCOBISS.SI-ID - 154225155
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JCR | SNIP | JCR | SNIP | JCR | SNIP | JCR | SNIP |
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Database name | Field | Year |
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Links to authors' personal bibliographies | Links to information on researchers in the SICRIS system |
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Ošep, Anka | ![]() |
Koban, Eva | ![]() |
Škerget, Matevž | 39671 |
Savšek, Lina | 56515 |
Source: Personal bibliographies
and: SICRIS
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