Desquamative interstitial pneumonitis and alveolar lipoproteinosis: Diagnostic difficulties and therapy problems with an infant
Identifieur interne : 003437 ( Main/Exploration ); précédent : 003436; suivant : 003438Desquamative interstitial pneumonitis and alveolar lipoproteinosis: Diagnostic difficulties and therapy problems with an infant
Auteurs : K. Schneider [Allemagne] ; I. Brünstler [Allemagne] ; H. Vogel [Allemagne] ; H. Fendel [Allemagne] ; K. Remberger [Allemagne]Source :
- European Journal of Pediatrics [ 0340-6199 ] ; 1986-12-01.
English descriptors
- KwdEn :
- Teeft :
- Alveolar lipoproteinosis, Alveolar spaces, Artificial ventilation, Bronchopulmonary lavage, Chest radiograph, Corticoid, Cytomegalovirus, Cytomegalovirus disease, Cytomegalovirus infection, Desquamative, Effective treatment, Federal republic, Fibrosing alveolitis, Herpes simplex, Hunter syndrome, Iduronate sulfatase, Immunologic function, Interstitial, Interstitial lung tissue, Interstitial pneumonitis, Lavage, Lipoproteinosis, Lung disease, Lung tissue, Open lung biopsy, Pneumocytes type, Pneumonitis, Proteinosis, Pulmonary alveolar proteinosis, Pulmonary involvement, Respiratory tract.
Abstract
Abstract: A desquamative, interstitial pneumonitis was diagnosed histologically in a 9-month-old boy who first became ill at the age of 5 weeks. The desquamative interstitial pneumonitis was associated with an acquired cytomegalovirus (CMV) infection. Despite treatment with corticoids, acyclovir and artificial ventilation, the patient died of pulmonary insufficiency at the age of 15 months. The autopsy revealed an alveolar lipoproteinosis.
Url:
DOI: 10.1007/BF02429072
Affiliations:
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Le document en format XML
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<front><div type="abstract" xml:lang="en">Abstract: A desquamative, interstitial pneumonitis was diagnosed histologically in a 9-month-old boy who first became ill at the age of 5 weeks. The desquamative interstitial pneumonitis was associated with an acquired cytomegalovirus (CMV) infection. Despite treatment with corticoids, acyclovir and artificial ventilation, the patient died of pulmonary insufficiency at the age of 15 months. The autopsy revealed an alveolar lipoproteinosis.</div>
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