Hemophagocytic syndrome following alemtuzumab treatment for multiple sclerosis: A case report

A. Romero, L. Midaglia, M. T. Salcedo, L. Viladomiu, E. Guillén, I. Bajaña, L. Escolà-Vergé, M. Tintoré, X. Montalban, O. Len*

*Autor corresponent d’aquest treball

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Resum

Background:: Alemtuzumab is a monoclonal antibody targeting CD-52, used for treating relapsing-remitting multiple sclerosis (RRMS). Methods:: We present a case of a 44-year-old male with RRMS who was admitted due to fever and jaundice after starting treatment with alemtuzumab 12 months ago. Results:: He was diagnosed with hemophagocytic syndrome (HS). Liver biopsy revealed images of hemophagocytosis in Kupffer cells of lobular sinusoid. Management consisted of treatment with corticosteroids. Conclusion:: HS is a severe condition marked by an excessive activation of the immune system that leads to a rapid and progressive multi-organ failure, so it is important to consider it in the differential diagnosis of a fever syndrome following the administration of alemtuzumab.

Idioma originalAnglès
Número d’article101973
RevistaMultiple Sclerosis and Related Disorders
Volum40
DOIs
Estat de la publicacióPublicada - de maig 2020

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