Primary intestinal lymphangiectasia as a component of autoimmune polyglandular syndrome type I: a report of 2 cases.
Artículo
en Inglés
| 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.
Texto completo:
Disponible
Índice:
IMSEAR (Asia Sudoriental)
Asunto principal:
Femenino
/
Humanos
/
Masculino
/
Poliendocrinopatías Autoinmunes
/
Resultado Fatal
/
Adulto
/
Diagnóstico Diferencial
/
Linfangiectasia Intestinal
Tipo de estudio:
Estudio diagnóstico
Idioma:
Inglés
Año:
2007
Tipo del documento:
Artículo
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