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Sacroiliitis and Spondylitis with Sternoclavicular yperostosis: SAPHO or an Ankylosing Spondylitis Variant? 被引量:2

Sacroiliitis and Spondylitis with Sternoclavicular yperostosis: SAPHO or an Ankylosing Spondylitis Variant?
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摘要 To the Editor: SAPHO syndrome is a heterogeneous disorder characterized by synovitis, ache, pustulosis, hyperostosis, and osteitis. Its diagnosis can be difficult if there are no typical skin manifestations. We reported a case of SAPHO syndrome which also fulfills the current diagnostic criteria, for ankylosing spondylitis (AS). To the Editor: SAPHO syndrome is a heterogeneous disorder characterized by synovitis, ache, pustulosis, hyperostosis, and osteitis. Its diagnosis can be difficult if there are no typical skin manifestations. We reported a case of SAPHO syndrome which also fulfills the current diagnostic criteria, for ankylosing spondylitis (AS).
出处 《Chinese Medical Journal》 SCIE CAS CSCD 2016年第1期110-111,共2页 中华医学杂志(英文版)
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  • 1Hayem G, Bouchaud-Chabot A, Benah K, Roux S, Palazzo E, Silbermann-Hoffman 0, et al. SAPHO syndrome: A long-term follow-up study 0[120 cases. SeminArthritis Rheum 1999;29:159-71. doi: 10.1016/S0049-0172(99)80027-4.
  • 2Leone A, Cassar-Pullicino VN, Casale R, Magarelli N, Semprini A, Colosimo C. The SAPHO syndrome revisited with an emphasis on spinal manifestations. Skeletal Radiol 2015;44:9-24. doi: 10.1007/ s00256-0 14-2025-0.
  • 3Maugars Y, Berthelot JM, Ducloux JM, Prost A. SAPHO syndrome: A followup study of 19 cases with special emphasis on enthesis involvement. J RheumatoI1995;22:2135-41.
  • 4Hukuda S, Minami M, Saito T, Mitsui H, Matsui N, Komatsubara Y, et al. Spondyloarthropathies in Japan: Nationwide questionnaire survey performed by the Japan Ankylosing Spondylitis Society. J Rheumato1200 1 ;28:554-9.
  • 5Takigawa T, Tanaka M, Nakanishi K, Misawa H, Sugimoto Y, Takahata T, et al. SAPHO syndrome associated spondylitis. Eur Spine J 2008;17:1391-7. doi: 10.1007/s00586-008-0722-x.

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