Abstract
Interstitial lung disease in children is uncommon. It usually presents with the gradual onset of increasing respiratory symptoms including tachypnoea, effort dyspnoea and cyanosis. In the acute situation there is alveolar infiltration with infecting organisms such as Pneumocystis carinii or viruses including Cytomegalovirus (CMV) and Ebstein-Barr virus (EBV) or fungi such as Aspergillus fumigatus or Candida albicans. These conditions result in widespread interstitial shadowing on the chest X-ray which is usually ‘ground-glass’ in appearance and bilateral in distribution. These acute conditions occur in children who are primarily immune deficient with cell mediated or humoral deficiency. Most commonly they occur in those who have reduced immunoglobulin or immunoglobulin subclasses. They are most common in those who have severe combined immune deficiency (SCID) and are now a main presenting feature in those who have human immune deficiency virus/acquired immune deficiency syndrome (HIV/AIDS) [1].
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Dinwiddie, R., Crawford, O., Sharief, N. (1999). Interstitial Lung Disease in Children. In: Sperber, M. (eds) Diffuse Lung Disorders. Springer, London. https://doi.org/10.1007/978-1-4471-3440-4_22
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DOI: https://doi.org/10.1007/978-1-4471-3440-4_22
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