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Thorax 60:665-671 doi:10.1136/thx.2004.027326
  • Interstitial lung disease

Chronic bird fancier’s lung: histopathological and clinical correlation. An application of the 2002 ATS/ERS consensus classification of the idiopathic interstitial pneumonias

  1. Y Ohtani1,
  2. S Saiki2,
  3. M Kitaichi3,
  4. Y Usui1,
  5. N Inase1,
  6. U Costabel4,
  7. Y Yoshizawa1
  1. 1Integrated Pulmonology, Tokyo Medical and Dental University, Tokyo, Japan
  2. 2Department of Pathology, Juntendou University Hospital, Tokyo, Japan
  3. 3Laboratory of Anatomic Pathology, Kyoto University Hospital, Kyoto, Japan
  4. 4Department of Pneumology/Allergy, Ruhrlandklinik, Essen, Germany
  1. Correspondence to:
    Professor Y Yoshizawa
    Integrated Pulmonology, Tokyo Medical and Dental University, 5-45, Yushima 1-chome, Bunkyo-ku, Tokyo 113-8519, Japan; yoshizawa.pulmtmd.ac.jp
  • Received 15 May 2004
  • Accepted 15 April 2005

Abstract

Background: Chronic bird fancier’s lung (BFL) has often been misdiagnosed as one of the idiopathic interstitial pneumonias (IIPs).

Methods: To define the clinical and pathological characteristics of chronic BFL, 26 patients with chronic BFL from whom a surgical lung biopsy specimen was taken between October 1992 and June 2001 were evaluated. The histopathological characteristics of the surgical lung biopsy specimens were examined and correlations between the histopathology and clinical characteristics were analysed. The quality of chronic inflammatory and fibrotic changes was expressed according to the 2002 ATS/ERS consensus classification of IIPs.

Results: Two patients were diagnosed as having bronchiolitis obliterans organising pneumonia (BOOP)-like lesions, five as having cellular non-specific interstitial pneumonia (NSIP)-like lesions, and eight as having fibrotic NSIP-like lesions. The other 11 patients were considered to have usual interstitial pneumonia (UIP)-like lesions because of the temporal heterogeneous appearances of the fibrotic changes. However, fibrosis in these patients had developed in centrilobular as well as perilobular areas, suggestive of hypersensitivity pneumonitis. Nineteen patients (73.1%) had multinucleated giant cells, often with cholesterol clefts, while only five patients (19.2%) had granulomas. Patients with BOOP-like or cellular NSIP-like lesions tended to have recurrent acute episodes, whereas patients with UIP-like lesions had an insidious onset. Patients with BOOP-like or cellular NSIP-like lesions had a more favourable outcome than those with fibrotic NSIP-like and UIP-like lesions.

Conclusions: The qualities of chronic inflammatory and fibrotic lesions vary significantly among patients with chronic BFL but correlate with clinical features and prognosis.

Footnotes

  • This work was supported by the Research Committee of the Japanese Ministry of Health and Welfare on Interstitial Pulmonary Disease, grant-in-aid for scientific research 12670552 from the Japanese Ministry of Education, the Research on Health Sciences focusing on Drug Innovation, and Charitable Trust of Okamoto Satoshi Fund for Fibrotic Lung Disorders.