ICD-10-CM J84: Other interstitial pulmonary diseases

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

acute idiopathic pulmonary hemorrhage in infants [AIPHI] (R04.81)

• pulmonary fibrosis (chronic) due to inhalation of chemicals, gases, fumes or vapors (J68.4)
• pulmonary fibrosis (chronic) following radiation (J70.1)

• lymphoid interstitial pneumonia (J84.2)
• pneumocystis pneumonia (B59)

non-specific interstitial pneumonia NOS, or due to known underlying cause (J84.89)

pneumocystis pneumonia (B59)

organizing pneumonia NOS, or due to known underlying cause (J84.89)

• exogenous lipoid pneumonia (J69.1)
• unspecified lipoid pneumonia (J69.1)

• cryptogenic organizing pneumonia (J84.116)
• idiopathic non-specific interstitial pneumonitis (J84.113)
• lipoid pneumonia, exogenous or unspecified (J69.1)
• lymphoid interstitial pneumonia (J84.2)

lung diseases due to external agents (J60-J70)

• underlying disease, such as:
• disorders of iron metabolism (E83.1-)

• underlying disease, such as:
• lung diseases due to external agents (J60-J70)
• rheumatoid arthritis (M05.00-M06.9)
• sarcoidosis (D86.-)
• systemic connective tissue disorders (M30-M36)

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

• , if applicable:
• poisoning due to drug or toxin (T51-T65 with fifth or sixth character to indicate intent), for toxic pneumonopathy
• underlying cause of pneumonopathy, if known

code, for adverse effect, to identify drug (T36-T50 with fifth or sixth character 5), if drug-induced

Essential brown induration of lung

• Capillary fibrosis of lung
• Cirrhosis of lung (chronic) NOS
• Fibrosis of lung (atrophic) (chronic) (confluent) (massive) (perialveolar) (peribronchial) NOS
• Induration of lung (chronic) NOS
• Postinflammatory pulmonary fibrosis

• Cryptogenic fibrosing alveolitis
• Idiopathic fibrosing alveolitis

Hamman-Rich syndrome

Progressive fibrotic interstitial lung disease

• 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

Lymphoid interstitial pneumonitis

Lymphangiomyomatosis

Adult PLCH

• Endogenous lipoid pneumonia
• Interstitial pneumonitis
• Non-specific interstitial pneumonitis NOS
• Organizing pneumonia NOS

Interstitial pneumonia NOS

, if applicable, associated condition