Organizing pneumonia
(Redirected from Cryptogenic organizing pneumonia)
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| Organizing pneumonia | |
|---|---|
| Diagnosis in short | |
 Organizing pneumonia. H&E stain. | |
|
| |
| LM | distal airway disease -- airways plugged with organizing exudate (fluffy light-staining paucicellular regions with stellate cells); no hobnailing of pneumocytes; type 2 pneumocytes hyperplasia is absent |
| LM DDx | diffuse alveolar damage (proliferative phase), bronchiolitis obliterans. |
| Site | lung - diffuse lung diseases |
|
| |
| Prevalence | uncommon |
| Prognosis | dependent on underlying cause |
| Clin. DDx | cryptogenic organizing pneumonia, transplant rejection, infection (pneumonia), collagen vascular disease, peri-tumour |
| Treatment | dependent on underlying cause |
Organizing pneumonia, abbreviated OP, is a histologic pattern in lung pathology. It fits into the larger category of diffuse lung diseases.
General
- Multiple causes, e.g. transplant rejection, infection.
Clinical diagnoses:[1]
- Transplant rejection.
- Cryptogenic organizing pneumonia (COP), AKA (idiopathic) bronchiolitis obliterans organizing pneumonia (BOOP).
- Should not be confused with constrictive bronchiolitis (AKA bronchiolitis obliterans).
- Collagen vascular disease.
- Toxic injury.
- Infection.
- Peri-tumour - in proximity to a space-occupying lesion (abscess, neoplasm).
Note:
- BOOP is used as a synonym for organizing pneumonia which has the long differential diagnosis above.[1]
- Confusingly, it may be used to refer to the idiopathic form of organizing pneumonia, now generally known as cryptogenic organizing pneumonia (COP).
- In other words, strictly speaking, BOOP is not the same as COP; idiopathic BOOP is COP.
- Confusingly, it may be used to refer to the idiopathic form of organizing pneumonia, now generally known as cryptogenic organizing pneumonia (COP).
Microscopic
Features:[2]
- Distal airway disease -- airways plugged with organizing exudate ("Masson bodies").
- "Organized exudate" = fluffy light-staining paucicellular regions with stellate cells (fibroblasts & immature connective tissue).
- No hobnailing of pneumocytes.
- Type 2 pneumocytes hyperplasia is absent.
DDx:
- Diffuse alveolar damage, proliferative phase - has type 2 pneumoncyte hyperplasia.
- Bronchiolitis obliterans.
Images
OP - very low mag. (WC/Nephron)
OP - low mag. (WC/Nephron)
OP - low mag. (WC/Nephron)
OP - intermed. mag. (WC/Nephron)
OP - intermed. mag. (WC/Nephron)
OP - high mag. (WC/Nephron)
Masson body
Masson body - intermed. mag. (WC/Nephron)
Masson body - high mag. (WC/Nephron)
Masson body - very high mag. (WC/Nephron)
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Lung, Right Lower Lobe, Open Lung Biopsy: - Organizing pneumonia. - Emphysematous changes. - NEGATIVE for significant pulmonary fibrosis. - NEGATIVE for malignancy. Comment: There is no evidence of granulomatous disease.
Micro
Organizing pneumonia with well-formed Masson bodies is seen subpleural and peribronchial. It is pathcy and mild. Significant fibrosis is absent. Eosinophils are not readily apparent.
See also
References
- ↑ 1.0 1.1 Humphrey, Peter A; Dehner, Louis P; Pfeifer, John D (2008). The Washington Manual of Surgical Pathology (1st ed.). Lippincott Williams & Wilkins. pp. 91. ISBN 978-0781765275.
- ↑ Klatt, Edward C. (2006). Robbins and Cotran Atlas of Pathology (1st ed.). Saunders. pp. 110. ISBN 978-1416002741.