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Related Experiment Videos

[Rheumatic manifestations of Behçet's disease].

S Benamour1

  • 1Service de Médecine Interne, CHU Ibn, Rochd, Casablanca, Maroc.

Annales De Medecine Interne
|January 19, 2000
PubMed
Summary

Joint manifestations are frequent in Behçet

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[Vogt-Koyanagi-Harada syndrome. Eight cases].

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[Neurological involvement in Behçet's disease. 154 cases from a cohort of 925 patients and review of the literature].

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[Macular damage in Behçet's disease].

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Joint manifestations in Behçet's disease. A review of 340 cases.

Revue du rhumatisme (English ed.)·1998
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[Ophthalmological involvement in Behçet disease. Apropos of 520 cases].

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Area of Science:

  • Rheumatology
  • Internal Medicine
  • Immunology

Context:

  • Behçet's disease is a multisystemic inflammatory disorder.
  • Rheumatologic symptoms, particularly joint involvement, are a common feature.
  • Joint manifestations can be the initial presentation of Behçet's disease.

Purpose:

  • To detail the spectrum of rheumatologic manifestations in Behçet's disease.
  • To highlight the diagnostic challenges posed by unusual joint presentations.
  • To emphasize the importance of recognizing these manifestations for timely diagnosis.

Summary:

  • Joint involvement is the third most common manifestation in Behçet's disease, often affecting knees and ankles, predominantly in males.
  • Presentations range from acute/recurrent monoarthritis and oligoarthritis to polyarthritis involving large and small joints.
  • Uncommon forms include destructive arthritis, pseudogout, popliteal cyst rupture, and myositis; while generally not requiring aggressive treatment, they can mimic other conditions.

Impact:

  • Enhances understanding of Behçet's disease rheumatology.
  • Aids clinicians in diagnosing challenging cases, especially when joint issues are the first sign.
  • Contributes to improved patient management by recognizing diverse joint presentations.

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