Primary intestinal lymphangiectasia as a component of autoimmune polyglandular syndrome type I: a report of 2 cases.
Article
Dans Anglais
| IMSEAR
| ID: sea-64066
ABSTRACT
Chronic diarrhea and steatorrhea occur frequently in patients with autoimmune polyglandular syndrome (APS) type I. Intestinal lymphangiectasia has been reported earlier as a cause of steatorrhea in a young girl with APS Type I. We describe 2 patients with APS Type I who were found to have intestinal lymphangiectasia, one of whom had symptomatic protein-losing enteropathy.
Texte intégral:
Disponible
Indice:
IMSEAR (Asie du Sud-Est)
Sujet Principal:
Femelle
/
Humains
/
Mâle
/
Polyendocrinopathies auto-immunes
/
Issue fatale
/
Adulte
/
Diagnostic différentiel
/
Lymphangiectasie intestinale
Type d'étude:
Etude diagnostique
langue:
Anglais
Année:
2007
Type:
Article
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