scholarly journals Progression of Cryptogenic Organizing Pneumonia to Pulmonary Fibrosis

Author(s):  
A.G. Dragnich ◽  
C.J. Scallan ◽  
L.A. Ho ◽  
B. Collins ◽  
S. Pipavath ◽  
...  
2004 ◽  
Vol 169 (1) ◽  
pp. 27-33 ◽  
Author(s):  
Elisa Lappi-Blanco ◽  
Riitta Kaarteenaho-Wiik ◽  
Sirpa Salo ◽  
Raija Sormunen ◽  
Marko Määttä ◽  
...  

2005 ◽  
Vol 12 (3) ◽  
pp. 153-161 ◽  
Author(s):  
Romain Lazor ◽  
Jean-Fran??ois Cordier

Author(s):  
Patricia López Pardo ◽  
Ana María Sánchez Peña ◽  
María Teresa Río Ramírez

2009 ◽  
Vol 137 (11-12) ◽  
pp. 681-683
Author(s):  
Natasa Miladinovic-Djukanovic ◽  
Jelena Djokovic ◽  
Nikola Torbica ◽  
Martin Popevic

Introduction. Cryptogenic organizing pneumonia is a particular form of inflammatory and fibroproliferative lung disease. The disease onset is subacute with cough, dyspnoea, fever, weight loss, and elevation of biological inflammatory markers. Chest imaging usually shows multifocal alveolar opacities predominating in the subpleural regions. Lung biopsy reveals budding connective tissue filling the distal airspaces. Case outline. A 57-year-old electrician complaining of cough, dyspnoea, and fatigue was diagnosed with pneumonia and treated with antibiotics and antihistaminics. After clinical and radiographic progression of the disease, open lung biopsy was performed, some 15 months after the disease onset. The diagnosis of cryptogenic organising pneumonia was made. The patient was treated with oral and inhalatory corticosteroids and finally with cytostatics, which led to a partial improvement of his condition. However, work capacity was lost and the quality of life seriously deteriorated. Conclusion. The diagnosis is established by combining clinical, radiological and histological criteria. Similarities with other disease processes can lead to a delayed or erroneous diagnosis. Most patients respond well to corticosteroid therapy (prednisone or methyl-prednisolone). Relapses are frequent but can generally be controlled.


Chest Imaging ◽  
2019 ◽  
pp. 463-468
Author(s):  
Cylen Javidan-Nejad

Organizing pneumonia (OP) is a nonfibrotic form of interstitial pneumonia that represents a manifestation of lung injury. It may be secondary to another process (such as vasculitis, collagen vascular disease, or drug therapy). When no inciting cause is found, the OP is believed to cryptogenic and the term Cryptogenic Organizing Pneumonia (COP) may be used clinically. Various patterns of OP may be encountered on imaging including classic (peripheral or bronchiolocentric consolidation), focal, crescentic, multinodular and fibrotic. The classic pattern is the most common, but the crescentic form (often known as the atoll or reverse halo sign) can be the most striking. The latter two patterns are more typical of OP associated with collagen vascular disease, most notably dermatomyositis and polymyositis.


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