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Fifteen years of treatment with intravenous immunoglobulin in central nervous system Langerhans cell histiocytosis.

Authors :
Gavhed, Désirée
Laurencikas, Evaldas
Åkefeldt, Selma O
Henter, Jan-Inge
Source :
Acta Paediatrica; Jul2011, Vol. 100 Issue 7, pe36-e39, 4p
Publication Year :
2011

Abstract

There is currently no well-accepted therapy for central nervous system Langerhans cell histiocytosis (CNS-LCH), a neuroinflammatory disease clinically characterized by often progressive, neurological symptoms including ataxia, dysarthria, dysphagia, hypertonicity, intellectual impairment and behavioural abnormalities. We applied immunomodulative/anti-inflammatory treatment on a patient with progressive CNS-LCH disease. Intravenous immunoglobulin (IVIG) was administered monthly for 15 years to a patient with severe, image-verified neurodegenerative CNS-LCH. During the IVIG treatment, the neurological deterioration initially appeared to be haltered, but over time there was still some deterioration. IVIG may be beneficial in partly haltering CNS-LCH neurodegeneration, but further studies are needed. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
08035253
Volume :
100
Issue :
7
Database :
Complementary Index
Journal :
Acta Paediatrica
Publication Type :
Academic Journal
Accession number :
60975190
Full Text :
https://doi.org/10.1111/j.1651-2227.2010.02125.x