The Journal of Clinical Pediatric Rheumatology
Online ISSN : 2434-608X
Print ISSN : 2435-1105
A case of familial Mediterranean fever with prolonged arthritis
Kyoko KuroiwaTomonari ShigemuraNorimoto KobayashiKenichi KoikeKiyoshi MigitaKazunaga Agematsu
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2010 Volume 3 Issue 2 Pages 77-80

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Abstract
  Typical familial Mediterranean fever(FMF)shows severe stomachache or chest/back pain accompanied with fever. Some FMF patients show arthritis, however, the detail has been unclear. We here analyzed the prolonged arthritis accompanied by FMF.25-year-old woman showed fever with stomachache,chest pain, and arthritis in the knees and the fbot, which healed in a few days since her childhood. On the basis of MEFV gene analysis revealing M6941/M6941 mutation, we made a diagnosed of FMF. After having colchicine, she had had only mild attacks. She had pain and remarkable swelling in the right knee. Arthrocentesis revealed that the synovial fluid was yellow and quite muddy,mainly including neutrophils. MRI fndings of the knee were slight growth of synovial membrane,stagnation of synovial fluid,but no bone destruction.She had colchicine continuously,thereafter,she had an arthritis with erysipelas like rash in the foot joint.The arthritis disappeared after three months.We rarely see joint destruction in FMF.This may be attributed to the only activation of neutrophils,in contrast to RA accompanied by articular destruction,in which T cell abnormalities were recognized.
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© 2010 Pediatric Rheumatology Association of Japan
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