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The bm12 Inducible Model of Systemic Lupus Erythematosus (SLE) in C57BL/6 Mice
Published on: November 1, 2015
Recurrent benign lymphocytic (mollaret) meningitis in systemic lupus erythematosus
Jamal Mikdashi1, Stacy Kennedy, Allan Krumholz
1Department of Medicine, University of Maryland School of Medicine, Baltimore, MD 21201, USA. jmikdash@umaryland.edu
Background:
Aseptic meningitis is one of the most infrequent neuropsychiatric manifestations of systemic lupus erythematosus (SLE) with multifactorial etiologies including medications such as nonsteroidal anti-inflammatory drugs, azathioprine, and trimethoprim-sulfamethoxasole, as well as viruses and malignancy. Recurrent aseptic meningitis in SLE is rare, and remains a diagnostic challenge.
Methods:
We report a unique SLE patient with recurrent (10 episodes), benign (self-limited) lymphocytic aseptic meningitis, which suggests the diagnosis of Mollaret meningitis. There was no prior use of medications known to provoke meningitis. No infectious etiology was identified and chronic meningitis was not observed. The patient had spontaneous resolution of symptoms with no neurologic sequelae.
Conclusion:
Recurrent benign lymphocytic aseptic meningitis is recognized in this SLE patient. We propose that noninfectious Mollaret meningitis be classified as a feature of neuropsychiatric SLE syndromes.
Insights
Systemic lupus erythematosus (SLE) can cause aseptic meningitis. A rare case of recurrent, benign lymphocytic aseptic meningitis in an SLE patient suggests a link to Mollaret meningitis.
Area of Science:
- Neurology
- Rheumatology
- Infectious Diseases
Background:
- Aseptic meningitis is a rare neuropsychiatric manifestation of systemic lupus erythematosus (SLE).
- Potential causes include medications, infections, and malignancy.
- Recurrent aseptic meningitis in SLE presents diagnostic challenges.
Observation:
- A unique case of a systemic lupus erythematosus (SLE) patient experiencing 10 episodes of recurrent, benign, self-limited lymphocytic aseptic meningitis is presented.
- The patient had no history of meningitis-inducing medications, and no infectious or chronic meningitis etiology was identified.
- Symptoms resolved spontaneously without neurological deficits.
Findings:
- The patient's presentation suggests Mollaret meningitis.
- Recurrent benign lymphocytic aseptic meningitis was confirmed in this SLE patient.
- The meningitis episodes were self-limited with complete recovery.
Implications:
- This case supports classifying noninfectious Mollaret meningitis as a neuropsychiatric manifestation of SLE.
- Recognizing this pattern can aid in diagnosing and managing similar complex cases in SLE patients.
- Further research into the pathogenesis of noninfectious Mollaret meningitis in SLE is warranted.
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