Relapsing polychondritis
From IDWiki
Background
- Rare autoimmune/inflammatory disorder
Clinical Manifestations
- Acute pain, swelling, and erythema of cartilage
- Episodes remit over weeks or months, and recur over years
- Most commonly of pinna (spares the other soft tissues), followed by nasal cartilage and arthritis
- Arthritis may be symmetric or asymmetric, large or small joint, but is typically non-deforming
- Other tissues may include:
- Eye, including conjunctivitis, scleritis, iritis, keratitis, and chorioretinitis
- Cartilage of the larynx, trachea, or bronchi
- Internal ear
- Cardiovascular system, including aortic regurgitation, mitral regurgitation, pericarditis, myocarditis, aortic aneurysm, and aortitis
- Kidney
- Skin
- May eventually lead to:
- Floppy ears
- Saddle nose deformity
- Pectus excavatum
- Visual, auditory, and vestibular abnormalities
- Tracheal narrowing and tracheal collapse
- Can occur in the context of systemic vasculitis (such as leukocytoclastic vasculitis or polyarteritis nodosa), myelodysplastic syndrome, or cancer is possible
Differential Diagnosis
Diagnostic Criteria
- Michet criteria require 2 major, or 1 major with 2 minor criteria
- Major criteria:
- Auricular cartilage inflammation
- Nasal cartilage inflammation
- Laryngotracheal cartilage inflammation
- Minor criteria:
- Seronegative arthritis
- Ocular inflammation
- Hearing loss
- Vestibular dysfunction
References
- ^ Clement J. Michet. Relapsing Polychondritis. Annals of Internal Medicine. 1986;104(1):74. doi:10.7326/0003-4819-104-1-74.