ATS GUIDELINES Bundle

Idiopathic Pulmonary Fibrosis Diagnosis

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5 Table 3. High-Resolution CT Scanning Patterns UIP Probable UIP Indeterminate for UIP Alternative Diagnosis Subpleural and basal predominant; distribution is oen heterogeneous a Honeycombing with or without peripheral traction bronchiectasis or bronchiolectasis b Subpleural and basal predominant; distribution is oen heterogeneous Reticular pattern with peripheral traction bronchiectasis or bronchiolectasis May have mild GGO Subpleural and basal predominant Subtle reticulation; may have mild GGO or distortion ("early UIP pattern") CT features and/or distribution of lung fibrosis that do not suggest any specific etiolog y ("truly indeterminate") Findings suggestive of another diagnosis, including : • CT features: ▶ Cysts ▶ Marked mosaic attenuation ▶ Predominant GGO ▶ Profuse micronodules ▶ Centrilobular nodules ▶ Nodules ▶ Consolidation • Predominant distribution: ▶ Peribronchovascular ▶ Perilymphatic ▶ Upper or mid-lung • Other: ▶ Pleural plaques (consider asbestosis) ▶ Dilated esophagus (consider CTD) ▶ Distal clavicular erosions (consider RA) ▶ Extensive lymph node enlargement (consider other etiologies) ▶ Pleural effusions, pleural thickening (consider CTD/drugs) a Variants of distribution: occasionally diffuse, may be asymmetrical. b Superimposed CT features: mild GGO, reticular pattern, pulmonary ossification.

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