FB82.3

ICD-11 MMS 2026-01

Relapsing polychondritis

Description

Relapsing polychondritis is a multisystem inflammatory disease of unknown aetiology affecting the cartilage. The disease is characterised by intermittent or fluctuant inflammatory manifestations due to inflammation of the cartilaginous structures, resulting in tissue damage and tissue destruction. Chondritis of auricular, nasal, tracheal cartilage predominates in this disease, suggesting response to tissue-specific antigens such as collagen II and cartilage matrix protein (matrillin-1). In about one third of patients, RP is associated with vasculitis (from isolated cutaneous leucocytoclastic vasculitis to systemic polyangiitis) and autoimmune rheumatic diseases (mainly rheumatoid arthritis and systemic lupus erythematosus). Haematological malignant diseases, gastrointestinal disorders and endocrine diseases may also occur. Functional and anatomical evaluation for upper and lower airway disease is essential in evaluation and management of the disease.

Index terms

  • Relapsing polychondritis

Exclusions from above levels

  • FC01 – postprocedural chondropathies
  • 01 – Certain infectious or parasitic diseases
  • 05 – Endocrine, nutritional or metabolic diseases
Show allHide
  • 18 – Complications of pregnancy, childbirth and the puerperium
  • 19 – Certain conditions originating in the perinatal period
  • 22 – Injury, poisoning or certain other consequences of external causes
  • DA0E.8 – Temporomandibular joint disorders

Sibling codes

  • FB82.0 – Chondromalacia
  • FB82.1 – Osteochondrosis or osteochondritis dissecans
  • FB82.2 – Slipped upper femoral epiphysis
  • FB82.Y – Other specified chondropathies
  • FB82.Z – Chondropathies, unspecified

Foundation entity

Relapsing polychondritis – http://id.who.int/icd/entity/1412888287

Part of: FB82: Chondropathies › 15: Diseases of the musculoskeletal system or connective tissue