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J84.178

Billable

Other interstitial pulmonary diseases with fibrosis in diseases classified elsewhere

HCC Category Mapping

V28HCC 280Chronic Obstructive Pulmonary Disease
0.334
V24HCC 112Fibrosis of Lung and Other Chronic Lung Disorders
0.268
ESRDHCC 112Fibrosis of Lung and Other Chronic Lung Disorders
0.000
RxHCCHCC 227Sarcoidosis, Pulmonary Alveolar Disorders
0.000

What This Code Means

Scarring and inflammation of lung tissue that occurs as a complication of another disease, affecting the lung's ability to function properly.

Coding Tips

  • Requires documentation of the primary disease causing the interstitial lung disease
  • Use when fibrosis is present but does not fit other more specific J84.17x codes

Clinical Significance

Other interstitial pulmonary diseases with fibrosis in diseases classified elsewhere captures fibrotic ILD manifestations of systemic diseases that do not meet the progressive fibrotic phenotype criteria. This secondary diagnosis code reflects the pulmonary fibrotic burden in patients with conditions like connective tissue diseases, sarcoidosis, or other systemic conditions affecting the lungs.

Documentation Requirements

  • Documentation of the underlying disease classified elsewhere causing the interstitial lung disease with fibrosis
  • Imaging evidence of fibrosis (high-resolution computed tomography showing reticular changes, honeycombing, or traction bronchiectasis)
  • Pulmonary function test results documenting the fibrotic impact
  • Documentation that the fibrosis is NOT progressive (if progressive, use J84.170 instead)
  • Code the underlying disease first, with this as a secondary/manifestation code

Code First

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

Commonly Confused Codes

Code Hierarchy

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