Successful treatment of systemic lupus erythematosus cerebritis with intravenous immunoglobulin

Y. Sherer, Y. Levy, P. Langevitz, M. Lorber, F. Fabrizzi, Y. Shoenfeld*

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

69 Scopus citations

Abstract

Neuropsychiatric lupus includes extremely diverse clinical manifestations, ranging from mild cognitive dysfunction to a severe, life- threatening presentation. We report a 28-year-old patient with systemic lupus erythematosus who had persistent fever for 3 months, and developed within a few hours motor and sensory aphasia, rotator nystagmus with deviation of the eyes, and severe nuchal rigitidy. An extensive series of imaging and laboratory tests were interpreted as normal, except for an elevated opening pressure at lumbar puncture, cerebrospinal fluid inflammatory findings, and asymmetrical cortical perfusion on single-photon emission computed tomography. The patient received one course of high-dose intravenous immunoglobulin (IVIg) and within 5 days her condition returned to that of 3 months before admission. The mechanisms of injury, along with the management of cerebral lupus and the mechanisms of action of IVIg, are discussed.

Original languageEnglish
Pages (from-to)170-173
Number of pages4
JournalClinical Rheumatology
Volume18
Issue number2
DOIs
StatePublished - 1999

Keywords

  • Autoantibodies
  • Autoimmunity
  • Intravenous immunoglobulin
  • Neuropsychiatric lupus
  • Systemic lupus erythematosus

Fingerprint

Dive into the research topics of 'Successful treatment of systemic lupus erythematosus cerebritis with intravenous immunoglobulin'. Together they form a unique fingerprint.

Cite this