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Idiopatisk pulmonal hæmosiderose hos et etårigt barn med Downs syndrom

Anna Elisabeth Lewis1, Christina Engel Høi-Hansen1, Frederik Buchvald2 & Werner Petersen1 1) Børne- og Ungeafdelingen, Nordsjællands Hospital, Hillerød 2) Dansk Børnelunge Center, BørneUnge-Klinikken, Rigshospitalet Ugeskr Læger 2014;176:V04140253
Ugeskr Læger 2014;176:V04140253
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Idiopathic pulmonary haemosiderosis in a one-year-old girl with Down syndrome
Idiopathic pulmonary haemosiderosis (IPH) is a rare disease. We describe a girl with Down syndrome who had no major respiratory symptoms until one year of age, where recurrent airway infections and chronic anaemia of unknown aetiology developed. At 20 months of age she had intermittent haemo­ptysis, was investigated with computed tomography and broncho-alveolar lavage and was diagnosed with IPH. After treatment, respiratory symptoms and anaemia resolved and a positive impact on previously impaired growth and psychomotor development was seen. Paediatricians should consider IPH in children with recurrent respiratory symptoms and anaemia.
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