Autoimmune pulmonary proteinosis in a Chilean teenager, a rare aetiology of interstitial lung disease

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dc.contributor.authorStrickler, A.
dc.contributor.authorBoza, M. L.
dc.contributor.authorKoppmann, A.
dc.contributor.authorGonzález Bombardiere, Sergio
dc.date.accessioned2020-01-14T01:29:01Z
dc.date.available2020-01-14T01:29:01Z
dc.date.issued2014
dc.description.abstractInterstitial lung disease (ILD) is rare and encompasses a heterogeneous group of diseases, and is even rarer in children than in adults. ILDs compromise more than 100 different entities, including pulmonary alveolar proteinosis (PAP). There are many causes of PAP in children, including surfactant protein gene mutations (SFTPB, SFTPC, ABCA3, TTF-1), GMCSF receptor mutations and antigranulocyte-macrophage colony-stimulating factor autoantibodies. We report a case of a 13-year-old Chilean girl who presented with an 8-month history of progressive exercise intolerance, fatigability and diminished school performance. Physical examination revealed resting tachypnoea, a few basal bilateral inspiratory crackles, and hypoxaemia on minimal exertion. Clinical suspicion and evaluation, including international collaboration, led to the diagnosis of autoimmune PAP and specific therapy for the condition.
dc.identifier.doi10.1136/bcr-2012-006987
dc.identifier.issn1757-790X
dc.identifier.urihttps://repositorio.uc.cl/handle/11534/27464
dc.language.isoes
dc.nota.accesoContenido parcial
dc.revistaBMJ Case Reportses_ES
dc.rightsacceso restringido
dc.subjectClarithromycines_ES
dc.subjectGranulocyte macrophage colony stimulating factores_ES
dc.subjectSalbutamoles_ES
dc.subjectABCA3 genees_ES
dc.subjectAdolescentes_ES
dc.subjectAntibody blood leveles_ES
dc.subjectArticlees_ES
dc.subjectAutoimmune diseasees_ES
dc.subjectAutoimmune pulmonary proteinosises_ES
dc.subjectCase reportes_ES
dc.subjectChilees_ES
dc.subjectComputer assisted tomographyes_ES
dc.subjectCracklees_ES
dc.subjectDemyelinating diseasees_ES
dc.subjectDifferential diagnosises_ES
dc.subjectDisease coursees_ES
dc.subjectDisease durationes_ES
dc.subjectDrug induced diseasees_ES
dc.subjectElectron microscopyes_ES
dc.subjectFatiguees_ES
dc.subjectFemalees_ES
dc.subjectFollow upes_ES
dc.subjectForced expiratory volumees_ES
dc.subjectGenees_ES
dc.subjectGene mutationes_ES
dc.subjectGMCSF genees_ES
dc.subjectHumanes_ES
dc.subjectHuman tissuees_ES
dc.subjectHypoxemiaes_ES
dc.subjectInterstitial lung diseasees_ES
dc.subjectLung alveolus proteinosises_ES
dc.subjectLung biopsyes_ES
dc.subjectLung diseasees_ES
dc.subjectLung lavagees_ES
dc.subjectLymphoproliferative diseasees_ES
dc.subjectMycoplasma pneumoniaees_ES
dc.subjectOxygen therapyes_ES
dc.subjectPhysical capacityes_ES
dc.subjectPriority journales_ES
dc.subjectRheumatic diseasees_ES
dc.subjectSFTPB genees_ES
dc.subjectSFTPC genees_ES
dc.subjectSpirometryes_ES
dc.subjectTachypneaes_ES
dc.subjectThorax radiographyes_ES
dc.subjectTIF1 genees_ES
dc.subjectTreatment outcomees_ES
dc.subjectVasculitises_ES
dc.subjectVideo assisted thoracoscopic surgeryes_ES
dc.subject.ddc610
dc.subject.deweyMedicina y saludes_ES
dc.titleAutoimmune pulmonary proteinosis in a Chilean teenager, a rare aetiology of interstitial lung diseasees_ES
dc.typeartículo
sipa.codpersvinculados99856
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