- Overview of Interstitial Lung Disease
- Drug-Induced Pulmonary Disease
- Overview of Eosinophilic Pulmonary Diseases
- Acute Eosinophilic Pneumonia
- Chronic Eosinophilic Pneumonia
- Löffler Syndrome
- Hypersensitivity Pneumonitis
- Overview of Idiopathic Interstitial Pneumonias
- Idiopathic Pulmonary Fibrosis (IPF)
- Desquamative Interstitial Pneumonia (DIP)
- Nonspecific Interstitial Pneumonia (NSIP)
- Cryptogenic Organizing Pneumonia (COP)
- Respiratory Bronchiolitis–Associated Interstitial Lung Disease (RBILD)
- Acute Interstitial Pneumonia (AIP)
- Lymphoid Interstitial Pneumonia (LIP)
- Idiopathic Pleuroparenchymal Fibroelastosis
- Lymphangioleiomyomatosis
- Pulmonary Alveolar Proteinosis
- Pulmonary Langerhans Cell Histiocytosis
Respiratory bronchiolitis–associated interstitial lung disease is a form of idiopathic interstitial pneumonia.
Most people who smoke develop a subclinical bronchiolitis characterized by mild or moderate inflammation of the small airways. The few patients who develop more severe inflammation with clinically significant interstitial disease are said to have RBILD. It primarily affects people in their 30s to 50s who smoke cigarettes. Male-to-female ratio is 2:1.
RBILD is characterized histologically by submucosal inflammation of the membranous and respiratory bronchioles manifested by the presence of tan-brown pigmented macrophages (resulting from increased iron content, as occurs in people who smoke), mucus stasis, and metaplastic cuboidal epithelium in bronchioles and alveoli. Alveolar septal scarring always occurs. Similar findings, however, occur in some hypersensitivity reactions, occupational lung exposures (usually due to mineral dusts), viral infections, and drug reactions.
RBILD also resembles desquamative interstitial pneumonia histologically, but in RBILD, inflammation is patchier and less extensive. The similarity of the 2 conditions has led to the suggestion that they are different manifestations of the same disease caused by cigarette smoking.
Symptoms and signs of RBILD
Symptoms of cough and breathlessness during exertion resemble those of other interstitial lung diseases, especially idiopathic pulmonary fibrosis, but are milder. Crackles on examination are the only physical finding.
Diagnosis of RBILD
Chest radiograph
High-resolution CT (HRCT)
Sometimes surgical lung biopsy
Diagnosis of respiratory bronchiolitis–associated interstitial lung disease is considered in patients who smoke and are being evaluated for interstitial lung disease. Diagnostic testing includes imaging tests and biopsy.
Chest radiograph findings include the following:
Bronchial wall thickening
Diffuse, fine reticular or nodular opacities
Prominent peribronchovascular interstitium
Small peripheral ring shadows
Small regular and irregular opacities
HRCT often shows centrilobular nodules and patchy areas of hazy ground-glass opacities.
A mixed obstructive-restrictive pattern is a common pulmonary function test finding, although results may be normal or show an isolated increase in residual volume. Routine laboratory tests are not helpful.
Lung biopsy (usually surgical) is sometimes obtained if the diagnosis remains unclear and a trial of smoking cessation has not decreased symptoms.
Treatment of RBILD
Smoking cessation
Treatment of respiratory bronchiolitis–associated interstitial lung disease is smoking cessation and avoidance of even passive cigarette smoke exposure, which may prevent improvement or lead to recurrence of the illness. There is only anecdotal evidence of the efficacy of glucocorticoids.
The natural clinical course of the disease is unknown, but prognosis is good with smoking cessation.