A case of idiopathic multicentric Castleman disease in an alemtuzumab-treated patient with MS.

Rolfes L, Pfeuffer S, Ruck T, Windhagen S, Oschlies I, Pavenstädt HJ, Angenendt L, Wiendl H, Krämer J, Meuth SG

Research article (journal) | Peer reviewed

Abstract

Alemtuzumab is an efficacious therapy for active relapsing-remitting MS (RRMS), but its use is complicated by the potential development of secondary autoimmunity.1 Recent data from phase 3 extension studies confirm thyroid autoimmunity as the most abundant entity of secondary autoimmunity found in up to 30%–40% of treated patients, with most events mild or moderate in severity. Here, we present a case of another lymphoproliferative syndrome, namely idiopathic multicentric Castleman disease (iMCD), after alemtuzumab treatment.

Details about the publication

JournalNeurology: Neuroimmunology and NeuroInflammation (Neurol Neuroimmunol Neuroinflamm)
Volume7
Issue1
StatusPublished
Release year2020 (01/03/2020)
Language in which the publication is writtenEnglish
DOI10.1212/NXI.0000000000000638
KeywordsAdult; Alemtuzumab; Castleman Disease; Humans; Immunologic Factors; Male; Multiple Sclerosis, Relapsing-Remitting

Authors from the University of Münster

Krämer, Julia
Department for Neurology
Wiendl, Heinz Siegfried
Department for Neurology