[Chronic interstitial pneumonitis].
Identifieur interne : 003F88 ( Main/Exploration ); précédent : 003F87; suivant : 003F89[Chronic interstitial pneumonitis].
Auteurs : Rui Almeida [Portugal] ; Guilhermina Reis ; Cristina Ferreira ; Ma José Oliveira ; Dulce Oliveira ; Paula Fernandes ; Paula Ferreira ; Simão Frutuoso ; Luísa Carreira ; Valter Alves ; Ant Nio Paiva ; Margarida GuedesSource :
- Revista portuguesa de pneumologia [ 0873-2159 ]
Descripteurs français
- KwdFr :
- MESH :
English descriptors
- KwdEn :
- MESH :
- diagnosis : Lung Diseases, Interstitial.
- therapy : Lung Diseases, Interstitial.
- Child, Preschool, Chronic Disease, Female, Humans.
Abstract
Interstitial lung disease includes a group of chronic diseases characterized by alterations in alveolar walls and loss of functional alveolar-capillary units. These are rare diseases in children, mostly with an unknown cause and associated with a high morbidity and mortality due to insufficient therapeutic effectiveness. The authors report a case of a previously healthy 3 years old child who presented with wheezing and severe respiratory insufficiency following a respiratory infection. The investigation performed led to the diagnosis of chronic interstitial pneumonitis. Several treatments have been tried (corticosteroids, hydroxychloroquine, N-acetylcysteine) without any obvious improvement.
DOI: 10.1016/s0873-2159(15)30579-1
PubMed: 15300314
Affiliations:
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Le document en format XML
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Oliveira</name></author><author><name sortKey="Oliveira, Dulce" sort="Oliveira, Dulce" uniqKey="Oliveira D" first="Dulce" last="Oliveira">Dulce Oliveira</name></author><author><name sortKey="Fernandes, Paula" sort="Fernandes, Paula" uniqKey="Fernandes P" first="Paula" last="Fernandes">Paula Fernandes</name></author><author><name sortKey="Ferreira, Paula" sort="Ferreira, Paula" uniqKey="Ferreira P" first="Paula" last="Ferreira">Paula Ferreira</name></author><author><name sortKey="Frutuoso, Simao" sort="Frutuoso, Simao" uniqKey="Frutuoso S" first="Simão" last="Frutuoso">Simão Frutuoso</name></author><author><name sortKey="Carreira, Luisa" sort="Carreira, Luisa" uniqKey="Carreira L" first="Luísa" last="Carreira">Luísa Carreira</name></author><author><name sortKey="Alves, Valter" sort="Alves, Valter" uniqKey="Alves V" first="Valter" last="Alves">Valter Alves</name></author><author><name sortKey="Paiva, Ant Nio" sort="Paiva, Ant Nio" uniqKey="Paiva A" first="Ant Nio" last="Paiva">Ant Nio 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qualifier="diagnostic" xml:lang="fr"><term>Pneumopathies interstitielles</term></keywords><keywords scheme="MESH" qualifier="therapy" xml:lang="en"><term>Lung Diseases, Interstitial</term></keywords><keywords scheme="MESH" xml:lang="en"><term>Child, Preschool</term><term>Chronic Disease</term><term>Female</term><term>Humans</term></keywords><keywords scheme="MESH" xml:lang="fr"><term>Enfant d'âge préscolaire</term><term>Femelle</term><term>Humains</term><term>Maladie chronique</term><term>Pneumopathies interstitielles</term></keywords></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">Interstitial lung disease includes a group of chronic diseases characterized by alterations in alveolar walls and loss of functional alveolar-capillary units. These are rare diseases in children, mostly with an unknown cause and associated with a high morbidity and mortality due to insufficient therapeutic effectiveness. The authors report a case of a previously healthy 3 years old child who presented with wheezing and severe respiratory insufficiency following a respiratory infection. The investigation performed led to the diagnosis of chronic interstitial pneumonitis. 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