Idiopathic pulmonary hemosiderosis.
Identifieur interne : 000016 ( Ncbi/Merge ); précédent : 000015; suivant : 000017Idiopathic pulmonary hemosiderosis.
Auteurs : T. Dua ; J. Chandra ; M. Jain ; S M Passah ; A K DuttaSource :
- Indian journal of pediatrics [ 0019-5456 ] ; 2000.
Descripteurs français
- KwdFr :
- Antirhumatismaux (usage thérapeutique), Chloroquine (usage thérapeutique), Enfant, Femelle, Hormones corticosurrénaliennes (usage thérapeutique), Humains, Hémosidérose (diagnostic), Hémosidérose (traitement médicamenteux), Maladies pulmonaires (diagnostic), Maladies pulmonaires (traitement médicamenteux), Mâle.
- MESH :
- diagnostic : Hémosidérose, Maladies pulmonaires.
- traitement médicamenteux : Hémosidérose, Maladies pulmonaires.
- usage thérapeutique : Antirhumatismaux, Chloroquine, Hormones corticosurrénaliennes.
- Enfant, Femelle, Humains, Mâle.
English descriptors
- KwdEn :
- MESH :
- chemical , therapeutic use : Adrenal Cortex Hormones, Antirheumatic Agents, Chloroquine.
- diagnosis : Hemosiderosis, Lung Diseases.
- drug therapy : Hemosiderosis, Lung Diseases.
- Child, Female, Humans, Male.
Abstract
Two cases of idiopathic pulmonary hemosiderosis in children are reported. Both cases presented with a combination of acute/recurrent respiratory symptoms along with iron deficiency anemia. In one case diagnosis was delayed for 18 months after onset of symptoms. After initial stabilisation with corticosteroid therapy, both cases were put on chloroquine therapy and showed improvement. Various other forms of therapy and outcome are discussed. It is suggested that in cases with recurrent respiratory symptoms, idiopathic pulmonary hemosiderosis should also be considered after excluding infectious etiology.
DOI: 10.1007/bf02762188
PubMed: 11028126
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- to stream PubMed, to step Corpus: 000479
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pubmed:11028126Le document en format XML
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<author><name sortKey="Passah, S M" sort="Passah, S M" uniqKey="Passah S" first="S M" last="Passah">S M Passah</name>
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<term>Chloroquine (therapeutic use)</term>
<term>Female</term>
<term>Hemosiderosis (diagnosis)</term>
<term>Hemosiderosis (drug therapy)</term>
<term>Humans</term>
<term>Lung Diseases (diagnosis)</term>
<term>Lung Diseases (drug therapy)</term>
<term>Male</term>
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<keywords scheme="KwdFr" xml:lang="fr"><term>Antirhumatismaux (usage thérapeutique)</term>
<term>Chloroquine (usage thérapeutique)</term>
<term>Enfant</term>
<term>Femelle</term>
<term>Hormones corticosurrénaliennes (usage thérapeutique)</term>
<term>Humains</term>
<term>Hémosidérose (diagnostic)</term>
<term>Hémosidérose (traitement médicamenteux)</term>
<term>Maladies pulmonaires (diagnostic)</term>
<term>Maladies pulmonaires (traitement médicamenteux)</term>
<term>Mâle</term>
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<keywords scheme="MESH" type="chemical" qualifier="therapeutic use" xml:lang="en"><term>Adrenal Cortex Hormones</term>
<term>Antirheumatic Agents</term>
<term>Chloroquine</term>
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<keywords scheme="MESH" qualifier="diagnosis" xml:lang="en"><term>Hemosiderosis</term>
<term>Lung Diseases</term>
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<term>Maladies pulmonaires</term>
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<keywords scheme="MESH" qualifier="drug therapy" xml:lang="en"><term>Hemosiderosis</term>
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<term>Chloroquine</term>
<term>Hormones corticosurrénaliennes</term>
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<term>Humans</term>
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<front><div type="abstract" xml:lang="en">Two cases of idiopathic pulmonary hemosiderosis in children are reported. Both cases presented with a combination of acute/recurrent respiratory symptoms along with iron deficiency anemia. In one case diagnosis was delayed for 18 months after onset of symptoms. After initial stabilisation with corticosteroid therapy, both cases were put on chloroquine therapy and showed improvement. Various other forms of therapy and outcome are discussed. It is suggested that in cases with recurrent respiratory symptoms, idiopathic pulmonary hemosiderosis should also be considered after excluding infectious etiology.</div>
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<DateRevised><Year>2019</Year>
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<Title>Indian journal of pediatrics</Title>
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<ArticleTitle>Idiopathic pulmonary hemosiderosis.</ArticleTitle>
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<Abstract><AbstractText>Two cases of idiopathic pulmonary hemosiderosis in children are reported. Both cases presented with a combination of acute/recurrent respiratory symptoms along with iron deficiency anemia. In one case diagnosis was delayed for 18 months after onset of symptoms. After initial stabilisation with corticosteroid therapy, both cases were put on chloroquine therapy and showed improvement. Various other forms of therapy and outcome are discussed. It is suggested that in cases with recurrent respiratory symptoms, idiopathic pulmonary hemosiderosis should also be considered after excluding infectious etiology.</AbstractText>
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<Reference><Citation>Pediatr Pulmonol. 1995 Aug;20(2):125-6</Citation>
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