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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.
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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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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