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J84.178

ICD-10-CM 2027 · Abrechenbar

Other interstitial pulmonary diseases with fibrosis in diseases classified elsewhere

Geschwistercodes

  • J84.170 – Interstitial lung disease with progressive fibrotic phenotype in diseases classified elsewhere

Code first

  • underlying disease, such as: progressive systemic sclerosis (M34.0)
  • rheumatoid arthritis (M05.00-M06.9)
  • systemic lupus erythematosis (M32.0-M32.9)

Inclusion terms

  • Interstitial pneumonia (nonspecific) (usual) due to collagen vascular disease
  • Interstitial pneumonia (nonspecific) (usual) in diseases classified elsewhere
  • Organizing pneumonia due to collagen vascular disease
  • Organizing pneumonia in diseases classified elsewhere

Vererbt von J84.1: Other interstitial pulmonary diseases with fibrosis

Code also

  • if applicable, pulmonary fibrosis (chronic) due to inhalation of chemicals, gases, fumes or vapors (J68.4)

Excludes1

  • pulmonary fibrosis (chronic) following radiation (J70.1)

Vererbt von J84: Other interstitial pulmonary diseases

Code also

  • if applicable, associated condition

Excludes1

  • drug-induced interstitial lung disorders (J70.2-J70.4)
  • interstitial emphysema (J98.2)

Excludes2

  • lung diseases due to external agents (J60-J70)

Teil von: J84.17: Other interstitial pulmonary diseases with fibrosis in diseases classified elsewhere › J84.1: Other interstitial pulmonary diseases with fibrosis › J84: Other interstitial pulmonary diseases