Management of Prominent Interstitial Markings at Lung Bases
The next step is to obtain high-resolution computed tomography (HRCT) of the chest to characterize the interstitial pattern and determine whether this represents early interstitial lung disease (ILD), interstitial lung abnormalities (ILAs), or a benign finding. 1
Initial Diagnostic Approach
HRCT Imaging is Mandatory
- HRCT is the essential next step to distinguish between various interstitial patterns and assess the extent and distribution of abnormalities 1
- Standard chest radiographs showing interstitial markings are insufficient for diagnosis and cannot reliably differentiate between various ILD patterns 1
- HRCT should be performed with:
Clinical Context Assessment
While obtaining HRCT, simultaneously evaluate for:
- Respiratory symptoms: Progressive dyspnea, chronic cough, or exercise intolerance that would suggest clinically significant ILD rather than incidental findings 1
- Exposure history: Occupational exposures, environmental antigens (for hypersensitivity pneumonitis), smoking history, and medication review 1
- Systemic disease screening: Connective tissue disease symptoms, as organizing pneumonia and interstitial patterns can occur with polymyositis, antisynthetase syndrome, and other autoimmune conditions 1, 2
HRCT Pattern Recognition Determines Next Steps
If HRCT Shows Definite UIP Pattern
- Honeycombing with subpleural and basal predominant reticular opacities with traction bronchiectasis establishes UIP pattern and may be sufficient for IPF diagnosis if other causes are excluded 1
- No lung biopsy needed if clinical context supports IPF and HRCT shows definite UIP 1
- Proceed to pulmonary function testing (spirometry with DLCO) to assess severity 1
If HRCT Shows Possible UIP or Indeterminate Pattern
- Multidisciplinary discussion (MDD) involving pulmonologist, radiologist, and pathologist is required to determine if surgical lung biopsy is indicated 1
- Video-assisted surgical lung biopsy should be considered if:
- Biopsy should sample 2-3 lobes due to potential histologic discordance 1
If HRCT Shows Alternative Patterns
- Ground-glass opacities with mosaic attenuation and relative basilar sparing suggest hypersensitivity pneumonitis—pursue antigen identification and consider bronchoscopy with bronchoalveolar lavage 1
- Peribronchovascular distribution with ground-glass opacities suggests nonspecific interstitial pneumonia (NSIP)—intensify search for connective tissue disease or drug exposure 1
- Organizing pneumonia pattern—investigate infectious, drug-related, radiation, or autoimmune etiologies before diagnosing cryptogenic organizing pneumonia 1, 2
If HRCT Shows Minimal Changes (ILAs)
- Interstitial lung abnormalities (ILAs) are defined as affecting <5% of any lung zone without meeting criteria for ILD 1
- If asymptomatic with normal pulmonary function, surveillance HRCT at 1-2 years is reasonable 1
- Consider genetic testing if family history of pulmonary fibrosis exists, as 15-30% of first-degree relatives have ILAs 1
Common Pitfalls to Avoid
- Do not delay HRCT: Plain radiograph interstitial markings are nonspecific and can represent technical factors, atelectasis, or early disease 1, 3
- Do not assume benign finding without HRCT confirmation: Even subtle interstitial markings can represent early progressive ILD 1
- Do not order lung biopsy before HRCT: Imaging must guide biopsy decisions and sampling locations 1
- Do not miss hypersensitivity pneumonitis: This requires specific questioning about bird exposure, hot tubs, mold, and occupational antigens, as it can mimic other ILDs but has different treatment 1
- Do not forget drug-induced ILD: Review all medications including over-the-counter supplements, as many drugs cause interstitial pneumonitis 1
Additional Baseline Testing
Concurrent with HRCT, obtain:
- Pulmonary function tests (spirometry, lung volumes, DLCO) to assess physiologic impairment 1
- Six-minute walk test with oxygen saturation monitoring to assess functional capacity and gas exchange 1
- Autoimmune serologies if connective tissue disease suspected (ANA, RF, anti-CCP, myositis panel, antisynthetase antibodies) 1
- Complete blood count: Eosinophilia may suggest drug reaction, parasitic infection, or eosinophilic pneumonia 1