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. 2021 Jan 11;7:594275. doi: 10.3389/fmed.2020.594275

Table 3.

Compares the characteristics of CBD with sarcoidosis across various clinical characteristics, lab abnormalities, and imaging studies.

Sarcoidosis Hypersensitivity pneumonitis (HP) CBD
Exposure
history
Unknown May have a history of an allergen exposure Exposure to beryllium;
Occupational history
Age of diagnosis Pea peak incidence at age of 20–39 years (49) The median age of diagnosis 65 years Mean age at time of diagnosis of CBD 43.9 (25–80) years (50)
Laboratory ACE level elevated (>80%) Serum IgG to potential antigens associated with HP (sensitivity and specificity of 83 and 68%) (48) ACE may be elevated in 22% case (44, 51).
BeLPT: abnormal (peripheral blood and/or BAL) (52)
Patch testing (BeSO4 or BeF): abnormal (peripheral blood and/or BAL)
Radiological - Symmetrical and bilateral Hilar LAD
- Nodules and/or Reticulonodular opacities
Features depend on subtype- non-fibrotic or fibrotic HP
- GGO, mosaic attenuation, centrilobular nodules, fibrosis (irregular linear opacities; traction bronchiectasis and honeycombing)
- Fibrosis is most severe in the mid or mid and lower lung zones or equally distributed in the three lung zones with relative basal sparing.
Head cheese sign/three-density pattern (47)
The most common radiographic abnormalities include diffuse small round and reticular opacities. Hilar adenopathy, linear scars, lung distortion, bullae, and pleural thickening are found less commonly associated (53)
Histopathology Well-formed, non-necrotizing granulomas, showing a lymphangitic distribution. Small and poorly formed granulomas, comprising loose, poorly circumscribed clusters of epithelioid and multinucleated cells (54). Bronchiolocentric inflammation
In Fibrotic HP-subpleural and centriacinar fibrosis, with or without bridging fibrosis. May have features that overlap with a UIP pattern (55)
Well-formed, non-necrotizing granulomas, and/or mononuclear cell interstitial cell infiltrates on endobronchial or transbronchial biopsy
Calcific inclusions reported
BALF Lymphocytic
CD4+:CD8+ ratio >3.5
Lymphocytic (>30% for non- and ex-smokers and >20% for current smokers) (56)
Low CD4+/CD8+ ratio (mean values of 0.5–1.5)
Increased expression of CD80/CD86 (48, 57)
Lymphocytosis 41–53% (44, 58)
BeLPT BAL
Spontaneous resolution Depends upon the stage Rare Rare
Treatment Immunosuppressants (corticosteroids) Removal from exposure - Corticosteroids (59) Removal from further exposure.
In symptomatic cases, corticosteroids/immunosuppressants

ACE, angiotensin converting enzyme; BALF, bronchoalveolar fluid; BeLPT, beryllium lymphocyte proliferation assay; CBD, chronic beryllium disease.