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Successful treatment of steroid-refractory neurosarcoidosis with infliximab

✍ Scribed by M. Sollberger; F. Fluri; T. Baumann; S. Sonnet; M. Tamm; A. J. Steck; M. Brutsche


Publisher
Springer
Year
2004
Tongue
English
Weight
213 KB
Volume
251
Category
Article
ISSN
0340-5354

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## Abstract Hemophagocytic lymphohistiocytosis (HLH) is a rare disorder characterized by fever, pancytopenia, hepatosplenomegaly, liver dysfunction, and hemophagocytosis. A 29‐year‐old woman, diagnosed with systemic lupus erythematosus in 1996, developed HLH in early June 2002. HLH remained refract