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[Pulmonary fibrosis in young patients with hypersensitivity pneumonitis]
Elzbieta Wiatr1, Elzbieta Radzikowska, Jacek Pawłowski
1III Kliniki Chorób Płuc.
Insights
Hypersensitivity pneumonitis (HP) can affect all ages, even children, often presenting as lung fibrosis. Early symptoms like cough and dyspnea on exertion are crucial for diagnosing this condition in young individuals.
Area of Science:
- Pulmonology
- Immunology
- Pediatrics
Background:
- Hypersensitivity pneumonitis (HP) is typically seen in middle-aged individuals, but can occur at any age.
- Host risk factors for HP remain poorly understood.
- This study focuses on young patients diagnosed with HP at the lung fibrosis stage.
Purpose of the Study:
- To present a series of 6 young patients diagnosed with hypersensitivity pneumonitis (HP) manifesting as advanced lung fibrosis.
- To highlight the diagnostic challenges and clinical presentations of HP in pediatric and young adult populations.
Main Methods:
- Case series presentation of 6 young patients (5 female, 1 male; ages 16-35) with diagnosed HP and lung fibrosis.
- Review of patient histories, clinical findings (asthenic build, scoliosis, clubbing), and diagnostic procedures.
- Serological testing for precipitins against common HP antigens (Farmer's lung, Pigeon fancier's lung).
- Radiological assessment (chest X-ray) to evaluate lung fibrosis extent.
Main Results:
- All 6 patients had long-term exposure to organic dust and presented with advanced lung fibrosis on chest X-ray.
- Precipitins against Farmer's lung and Pigeon fancier's lung antigens were detected in all patients.
- Despite steroid treatment, no improvement was observed in any patient, and two patients died.
Conclusions:
- Hypersensitivity pneumonitis (HP) should be considered in the differential diagnosis of interstitial lung diseases, particularly in young patients presenting with fibrosis.
- Chronic HP in children may initially manifest with symptoms such as cough and dyspnea on exertion.
Unlabelled:
Hypersensitivity pneumonitis (HP) is more common in middle-aged individuals but has been also diagnosed in patients of all ages including infants and children. Host risk factors are poorly characterized. The aim of this paper is presentation of 6 young patients in whom HP was diagnosed at the stage of lung fibrosis. There were 5 females at the age of 16-35 years and 1 male at the age of 28 years. All of them were exposed to organic dust for many years. Three of them were asthenic with scoliosis, 5 had clubbing. All patients were released from sport exercises in school due to fatigue but the diagnostic procedures were started at that time only in 2 patients. One woman had been ill from early childhood (recurrent pneumonia was recognised). In the another girl (16 years old) the spontaneous pneumothorax was the cause of the first chest X-ray examination. In the next woman (21 years old) marked dyspnea was connected with pregnancy and massive fibrotic lesions were recognised after delivery of her child. The only man was diagnosed before change of his job; he had no complaints. Two oldest women (34 and 35 years old) were diagnosed in childhood but avoidance of antigen exposure and corticotherapy were not effective. In all patients precipitins against farmer's lung and pigeon fancier's lung antigens were found. In all patients chest X-ray showed features of advanced lung fibrosis. All patients were treated with steroids without improvement. Two patients died during corticotherapy.
Conclusions:
1) HP could be taken into consideration during differential diagnosis of interstitial lung diseases, 2) Cough and dyspnea on exertion could be the first symptoms of chronic HP in children also.
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