Relapsing polychondritis is a rare and potentially fatal autoimmune disease of unknown etiology, characterized by inflammation and destruction of different cartilaginous structures, including the ear, nose, larynx, trachea, bronchi, peripheral joints, eye, heart and skin, with high risk of misdiagnosis. The spectrum of clinical presentations is protean and may vary from intermittent episodes of painful and disfiguring auricular and nasal chondritis or polyarthritis to severe progressive multi-organ damage. A laryngotracheobronchial involvement appears in nearly half of patients and is complicated by local obstructions, which may be life-threatening. A highly medical specialized approach is required for diagnosis of relapsing polychondritis. This review comprehensively examines the literature related to the clinical sceneries of the disease and focuses on both diagnostic tools used in clinical studies and recent findings related to its etiopathogenesis.
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|Titolo:||Diagnosis and classification of relapsing polychondritis.|
|Citazione:||Cantarini, L., Vitale, A., Brizi, M.g., Caso, F., Frediani, B., Punzi, L., et al. (2014). Diagnosis and classification of relapsing polychondritis. JOURNAL OF AUTOIMMUNITY, 48-49, 53-59.|
|Appare nelle tipologie:||1.1 Articolo in rivista|