J84 ICD 10 Code is a non-billable and non-specific code and should not be used to indicate a diagnosis for reimbursement purposes. There are other codes below it with greater level of diagnosis detail. The 2023 edition of the American ICD-10-CM code became effective on October 1, 2022.
Type 1 excludes for J84 ICD 10 code
- drug-induced interstitial lung disorders (J70.2-J70.4)
- interstitial emphysema (J98.2)
Type 2 excludes for J84 ICD 10 code
- lung diseases due to external agents (J60-J70)
Codes
- J84.0 Alveolar and parieto-alveolar conditions
- J84.01 Alveolar proteinosis
- J84.02 Pulmonary alveolar microlithiasis
- J84.03 Idiopathic pulmonary hemosiderosis
- J84.09 Other alveolar and parieto-alveolar conditions
- J84.1 Other interstitial pulmonary diseases with fibrosis
- J84.10 Pulmonary fibrosis, unspecified
- J84.11 Idiopathic interstitial pneumonia
- J84.111 Idiopathic interstitial pneumonia, not otherwise specified
- J84.112 Idiopathic pulmonary fibrosis
- J84.113 Idiopathic non-specific interstitial pneumonitis
- J84.114 Acute interstitial pneumonitis
- J84.115 Respiratory bronchiolitis interstitial lung disease
- J84.116 Cryptogenic organizing pneumonia
- J84.117 Desquamative interstitial pneumonia
- J84.17 Other interstitial pulmonary diseases with fibrosis in diseases classified elsewhere
- J84.170 Interstitial lung disease with progressive fibrotic phenotype in diseases classified elsewhere
- J84.178 Other interstitial pulmonary diseases with fibrosis in diseases classified elsewhere
- J84.2 Lymphoid interstitial pneumonia
- J84.8 Other specified interstitial pulmonary diseases
- J84.81 Lymphangioleiomyomatosis
- J84.82 Adult pulmonary Langerhans cell histiocytosis
- J84.83 Surfactant mutations of the lung
- J84.84 Other interstitial lung diseases of childhood
- J84.841 Neuroendocrine cell hyperplasia of infancy
- J84.842 Pulmonary interstitial glycogenosis
- J84.843 Alveolar capillary dysplasia with vein misalignment
- J84.848 Other interstitial lung diseases of childhood
- J84.89 Other specified interstitial pulmonary diseases
- J84.9 Interstitial pulmonary disease, unspecified
Possible back-references that may be applicable or related to J84 ICD10 Code:
- J00-J99 Diseases of the respiratory system
- J80-J84 Other respiratory diseases principally affecting the interstitium
Present On Admission (POA Exempt)
J84 ICD 10 code is considered exempt from POA reporting
Clinical information about J84 ICD 10 code
Interstitial lung disease is the name for a large group of diseases that inflame or scar the lungs. The inflammation and scarring make it hard to get enough oxygen. The scarring is called pulmonary fibrosis.
Breathing in dust or other particles in the air is responsible for some types of interstitial lung diseases. Specific types include:
- Black lung disease among coal miners, from inhaling coal dust
- Farmer's lung, from inhaling farm dust
- Asbestosis, from inhaling asbestos fibers
- Siderosis, from inhaling iron from mines or welding fumes
- Silicosis, from inhaling silica dust
Other causes include autoimmune diseases or occupational exposures to molds, gases, or fumes. Some types of interstitial lung disease have no known cause.
Treatment depends on the type of exposure and the stage of the disease. It may involve medicines, oxygen therapy, or a lung transplant in severe cases.
The information in this box was provided by MedlinePlus.gov