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Published on: November 23, 2013
Periodic meningitis and familial Mediterranean fever
Abstract:
A 33-year-old man had had, since he was 20 years old, recurrent attacks of fever, rash, and aseptic lymphocytic meningitis. A nephrotic syndrome developed that was found, on renal biopsy, to be due to amyloid deposit. After colchicine therapy, no further recurrence of fever and meningitis was observed. These findings suggest that aseptic periodic meningitis (Mollaret's syndrome) should be considered as an unusual manifestation of familial Mediterranean fever.
Insights
Familial Mediterranean fever can manifest as recurrent aseptic meningitis and nephrotic syndrome. Colchicine therapy effectively treated these symptoms, suggesting a link between Mollaret's syndrome and FMF.
Area of Science:
- Neurology
- Rheumatology
- Nephrology
Background:
- Recurrent aseptic lymphocytic meningitis, fever, and rash are key symptoms.
- Nephrotic syndrome can develop, indicating renal involvement.
Observation:
- A 33-year-old male patient presented with a 13-year history of recurrent meningitis, fever, and rash.
- Renal biopsy revealed amyloid deposits causing nephrotic syndrome.
Findings:
- Colchicine treatment led to the cessation of recurrent fever and meningitis episodes.
- The patient's clinical presentation suggests an unusual manifestation of familial Mediterranean fever.
Implications:
- Aseptic periodic meningitis (Mollaret's syndrome) should be considered in the differential diagnosis of familial Mediterranean fever.
- This case highlights the diverse clinical spectrum of FMF and the efficacy of colchicine in managing its varied manifestations.
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