Cases in which a diagnosis of “other” was made by more than one observer (n = 10)
| Diagnosis (no of times made) | No of patients | No of biopsies | Other diagnoses |
|---|---|---|---|
| LCG = Langerhans’ cell granulomatosis; DIP = desquamative interstitial pneumonia; DAD = diffuse alveolar damage, non-diag = non-diagnostic; NSIP = non-specific interstitial pneumonia; EPN = eosinophilic pneumonia; OP = organising pneumonia; LS/E = lymphangiomatosis/lymphangectasia; UNCL = unclassifiable; FB = follicular bronchiolitis; RB = respiratory bronchiolitis, Pulm haemosid = pulmonary haemosiderosis; EAA = extrinsic allergic alveolitis; UIP = usual interstitial pneumonia; LAM = lymphangioleiomyomatosis; EMPH = emphysema; CB = chronic bronchiolitis; BO = bronchiolitis obliterans; PPH = primary pulmonary hypertension; BPN = bronchopneumonia. | |||
| Figures in parentheses indicate the number of occasions that an individual diagnosis was made (maximum of 10). | |||
| LCG (4) | 1 | 1 | DIP, DAD (2), Non-diag, NSIP |
| EPN (5) | 1 | 1 | DAD (2), OP (2), DIP (1) |
| LS/E (6) | 1 | 1 | UNCL (2), FB (1), RB (1) |
| IPH (6) | 1 | 1 | NSIP (2), DIP (1), FB (1) |
| Amyloid (10) | 1 | 1 | – |
| LAM (17) | 1 | 2 | EMPH (2), Normal (1) |
| CB (6) | 1 | 3 | UNCL (9), NSIP (11), Non-diag (2), EAA (2) |
| BO (1), CB (1), PPH (1) | 1 | 1 | FB (7) |
| BPN (3) EPN (2) BO (1) | 1 | 1 | NSIP (2), UIP (1), EAA (2), UNCL (1) |
| BO (1) LCG (1) | 1 | 1 | OP (5), UIP (1), NSIP (2) |