Intestinal lymphangiectasia--a report in two Chinese children.
Identifieur interne : 006035 ( PubMed/Checkpoint ); précédent : 006034; suivant : 006036Intestinal lymphangiectasia--a report in two Chinese children.
Auteurs : S H Quak ; A. Wee ; H K Yap ; J S Tay ; T C Quah ; W C YipSource :
- Australian paediatric journal [ 0004-993X ] ; 1984.
Descripteurs français
- KwdFr :
- MESH :
- anatomopathologie : Entéropathie exsudative, Intestin grêle, Lymphangiectasie intestinale.
- Endoscopie, Femelle, Humains, Mâle, Nourrisson.
English descriptors
- KwdEn :
- MESH :
- pathology : Intestine, Small, Lymphangiectasis, Intestinal, Protein-Losing Enteropathies.
- Endoscopy, Female, Humans, Infant, Male.
Abstract
Two Chinese infants with asymmetrical lymphoedema and steatorrhoea were investigated. The laboratory investigations showed that they had hypoproteinaemia without proteinuria. One of them showed peripheral lymphopenia and hypogammaglobulinaemia. Radiologically, they had evidence of extensive lymphangiectasia of the small intestine. This was confirmed histologically. Endoscopy of one of them showed diffuse milky nodular duodenal mucosa. The appearance of the mucosa was rather typical of intestinal lymphangiectasia.
PubMed: 6466232
Affiliations:
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pubmed:6466232Le document en format XML
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<author><name sortKey="Yap, H K" sort="Yap, H K" uniqKey="Yap H" first="H K" last="Yap">H K Yap</name>
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<author><name sortKey="Tay, J S" sort="Tay, J S" uniqKey="Tay J" first="J S" last="Tay">J S Tay</name>
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<author><name sortKey="Quah, T C" sort="Quah, T C" uniqKey="Quah T" first="T C" last="Quah">T C Quah</name>
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<author><name sortKey="Yip, W C" sort="Yip, W C" uniqKey="Yip W" first="W C" last="Yip">W C Yip</name>
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<term>Lymphangiectasis, Intestinal (pathology)</term>
<term>Male</term>
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<keywords scheme="KwdFr" xml:lang="fr"><term>Endoscopie</term>
<term>Entéropathie exsudative (anatomopathologie)</term>
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<term>Intestin grêle (anatomopathologie)</term>
<term>Lymphangiectasie intestinale (anatomopathologie)</term>
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<keywords scheme="MESH" qualifier="anatomopathologie" xml:lang="fr"><term>Entéropathie exsudative</term>
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<term>Lymphangiectasie intestinale</term>
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<keywords scheme="MESH" qualifier="pathology" xml:lang="en"><term>Intestine, Small</term>
<term>Lymphangiectasis, Intestinal</term>
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<term>Humans</term>
<term>Infant</term>
<term>Male</term>
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<keywords scheme="MESH" xml:lang="fr"><term>Endoscopie</term>
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<term>Humains</term>
<term>Mâle</term>
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<front><div type="abstract" xml:lang="en">Two Chinese infants with asymmetrical lymphoedema and steatorrhoea were investigated. The laboratory investigations showed that they had hypoproteinaemia without proteinuria. One of them showed peripheral lymphopenia and hypogammaglobulinaemia. Radiologically, they had evidence of extensive lymphangiectasia of the small intestine. This was confirmed histologically. Endoscopy of one of them showed diffuse milky nodular duodenal mucosa. The appearance of the mucosa was rather typical of intestinal lymphangiectasia.</div>
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<Title>Australian paediatric journal</Title>
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<Abstract><AbstractText>Two Chinese infants with asymmetrical lymphoedema and steatorrhoea were investigated. The laboratory investigations showed that they had hypoproteinaemia without proteinuria. One of them showed peripheral lymphopenia and hypogammaglobulinaemia. Radiologically, they had evidence of extensive lymphangiectasia of the small intestine. This was confirmed histologically. Endoscopy of one of them showed diffuse milky nodular duodenal mucosa. The appearance of the mucosa was rather typical of intestinal lymphangiectasia.</AbstractText>
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