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Postgraduate Medical Journal 2004;80:339-345; doi:10.1136/pgmj.2003.012435
Copyright © 2004 The Fellowship of Postgraduate Medicine.
Postgraduate Medical Journal 2004;80:339-345
© 2004 Fellowship of Postgraduate Medicine

ORIGINAL ARTICLE

Clues for the differential diagnosis of hypersensitivity pneumonitis as an expectant variant of diffuse parenchymal lung disease

E Küpeli, D Karnak, O Kayacan and S Beder

Ankara University School of Medicine, Department of Chest Diseases, Ankara, Turkey

Correspondence to:
Correspondence to:
Dr Demet Karnak
Ankara University School of Medicine, Department of Chest Diseases, 06100 Cebeci, Ankara/Turkey; karnak{at}medicine.ankara.edu.tr

Hypersensitivity pneumonitis, also called extrinsic allergic alveolitis, a type of diffuse parenchymal lung disease (DPLD), is an immunologically mediated pulmonary disease induced by inhalation of various antigens. As data on the frequency of hypersensitivity pneumonitis are lacking in Turkey, a retrospective analyses was performed in 43 patients with DPLD, followed up over seven years. The objective was to discover cases fulfilling the diagnostic criteria for hypersensitivity pneumonitis, to determine the frequency and/or the new characteristics of the disease, and to pick up clues for differentiating it from other DPLDs. The four subjects with hypersensitivity pneumonitis (9%) who lived in an urban area were studied in detail. The most common symptoms were dry cough and dyspnoea. According to the symptom duration, clinical features, radiological and pathological findings, three were diagnosed with chronic and one with subacute hypersensitivity pneumonitis. Patients with hypersensitivity pneumonitis and those with DPLD were compared by means of age, sex, smoking status, symptom duration, haematology, erythrocyte sedimentation rate, peripheral cell count, spirometric parameters, blood gases, and diffusion capacity. No statistically significant difference was detected in these parameters except for forced expiratory volume in one second (FEV1) and forced vital capacity (FVC). In conclusion, patients with a history of antigen exposure, with mild symptoms such as dry cough and dyspnoea, and who have diffuse interstitial lung involvement on radiology should be carefully evaluated for hypersensitivity pneumonitis. Moreover, among other DPLDs, stable FEV1 or FVC values may be the clues for establishing the diagnosis of hypersensitivity pneumonitis. However, further studies are needed in larger series of patients.

Abbreviations: DLCO, diffusion capacity of the lung for carbon monoxide; DPLD, diffuse parenchymal lung disease; FEV1, forced expiratory volume in one second; FVC, forced vital capacity

Keywords: hypersensitivity pneumonitis; diffuse parenchymal lung disease; interstitial lung disease


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