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Published in: Orphanet Journal of Rare Diseases 1/2013

Open Access 01-12-2013 | Research

Hypersensitivity pneumonitis: lessons for diagnosis and treatment of a rare entity in children

Authors: Matthias Griese, Melanie Haug, Dominik Hartl, Veronika Teusch, Judith Glöckner-Pagel, Frank Brasch, the National EAA Study Group

Published in: Orphanet Journal of Rare Diseases | Issue 1/2013

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Abstract

Hypersensitivity pneumonitis (HP) also called exogenous allergic alveolitis = extrinsic allergic alveolitis in children is an uncommon condition and may not be recognized and treated appropriately.
To assess current means of diagnosis and therapy and compare this to recommendations, we used the Surveillance Unit for Rare Paediatric Disorders (ESPED) to identify incident cases of HP in Germany during 2005/6. In addition, cases of HP reported for reference from all over Germany to our center in the consecutive year were included.
Twenty-three children with confirmed pediatric HP were identified. All (age 9.4 y (4.4-15.1) presented with dyspnoea at rest or with exercise, mean FVC was 39% of predicted, seven of the 23 children already had a chronic disease state at presentation. IgG against bird was elevated in 20, and against fungi in 15. Bronchoalveolar lavage was done in 18 subjects (41% lymphocytes, CD4/CD8 1.99), and lung biopsy in 6. Except 2, all children were treated with prolonged courses of systemic steroids. Outcome was not favourable in all cases.
Late diagnosis in up to a quarter of the children with HP and inappropriate steroid treatment must be overcome to improve management of HP. Inclusion of children with HP into international, web-based registry studies will help to study and follow up such rare lung diseases.
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Metadata
Title
Hypersensitivity pneumonitis: lessons for diagnosis and treatment of a rare entity in children
Authors
Matthias Griese
Melanie Haug
Dominik Hartl
Veronika Teusch
Judith Glöckner-Pagel
Frank Brasch
the National EAA Study Group
Publication date
01-12-2013
Publisher
BioMed Central
Published in
Orphanet Journal of Rare Diseases / Issue 1/2013
Electronic ISSN: 1750-1172
DOI
https://doi.org/10.1186/1750-1172-8-121

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