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Diseases

Genetic and Rare Diseases Information Center (GARD)

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Cryptogenic organizing pneumonia

Other Names for this Disease
  • COP
  • Idiopathic BOOP
  • Idiopathic bronchiolitis obliterans organizing pneumonia
More Names
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Overview


Cryptogenic organizing pneumonia (COP) is a rapidly developing inflammatory lung disease characterized by flu-like symptoms including cough, fever, malaise, fatigue and weight loss. COP often affects adults in midlife (40 to 60 years of age). No predisposing factors have been identified and the cause is often unknown. Diagnosis may be made through computed tomography (CT) scan or lung biopsy. Response to treatment with corticosteroids is generally favorable.[1][2]


References

  1. Cordier JF, Costabel U, du Bois R. Cryptogenic organizing pneumonia. Orphanet. http://www.orphanet.net/consor/cgi-bin/OC_Exp.php?lng=EN&Expert=1302. Accessed November 4, 2011.
  2. King TE. Idiopathic Interstitial Pneumonias. The Merck Manual Home Health Handbook. http://www.merckmanuals.com/home/lung_and_airway_disorders/interstitial_lung_diseases/idiopathic_interstitial_pneumonias.html. Accessed November 4, 2011.
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  • The Merck Manuals Online Medical Library provides information on this condition. Click on the link to view the information.
  • The National Organization for Rare Disorders (NORD) is a federation of more than 130 nonprofit voluntary health organizations serving people with rare disorders. Click on the link to view information on this topic.
  • Orphanet is a European reference portal for information on rare diseases and orphan drugs.  Access to this database is free of charge.  Click on the link to read information on this topic.
  • PubMed is a searchable database of medical literature and lists journal articles that discuss Cryptogenic organizing pneumonia. Click on the link to view a sample search on this topic.