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Diagnosis of Interstitial Lung Disease Caused by Possible Hypersensitivity Pneumonitis in a Child: Think CGD

  • Saliha Esenboga*
  • , Nagehan Emiralioglu
  • , Deniz Cagdas
  • , Baran Erman
  • , Martin de Boer
  • , Berna Oguz
  • , Nural Kiper
  • , İlhan Tezcan
  • *Corresponding author for this work
  • Hacettepe University
  • University of Amsterdam

Research output: Contribution to journalComment/Letter to the editorAcademic

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Abstract

Interstitial lung disease (ILD) is a rare and heterogeneous group of disorder affecting the lung parenchyma and has a detrimental effect on gas exchange. Chronic granulomatous disease (CGD), when it affects primarily lungs, may cause ILD. We report a 16-year-old patient with CGD caused by homozygous deletion of NCF1 who atypically presented with ILD. The patient had many pigeons and was a pigeon breeder. Exacerbated clinical symptoms were linked to hypersensitivity pneumonitis (HP), and the patient was suggested to keep away from pigeons. In addition to allergen avoidance and prophylactic antibacterial therapy, treatment with corticosteroids and hydroxychloroquine was started for mainly obstructive and persistant symptoms of ILD. CGD is known to cause a hyperinflammatory state and the patients present with excessive granuloma formation and HP. Control of inflammation either by avoidance of allergen exposure and by anti-inflammatory drugs is necessary for the relief of symptoms.
Original languageEnglish
Pages (from-to)269-272
JournalJournal of clinical immunology
Volume37
Issue number3
DOIs
Publication statusPublished - 1 Apr 2017
Externally publishedYes

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

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