Cargando…
Primary intestinal lymphangiectasia (Waldmann's disease)
Primary intestinal lymphangiectasia (PIL) is a rare disorder characterized by dilated intestinal lacteals resulting in lymph leakage into the small bowel lumen and responsible for protein-losing enteropathy leading to lymphopenia, hypoalbuminemia and hypogammaglobulinemia. PIL is generally diagnosed...
Autores principales: | Vignes, Stéphane, Bellanger, Jérôme |
---|---|
Formato: | Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2008
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2288596/ https://www.ncbi.nlm.nih.gov/pubmed/18294365 http://dx.doi.org/10.1186/1750-1172-3-5 |
Ejemplares similares
-
Complicated primary intestinal lymphangiectasia (Waldmann's disease) in a child successfully treated with octreotide: A case report from a low-resource setting
por: El Haddar, Zohair, et al.
Publicado: (2021) -
Newfound features associated with Hennekam Syndrome (Intestinal Lymphangiectasia–Lymphedema–Intellectual–Disability Syndrome) complicated with comorbid Waldmann's Disease resulting in Celiac Disease
por: Safari Vejin, Tannaz, et al.
Publicado: (2023) -
The Update of Treatment for Primary Intestinal Lymphangiectasia
por: Kwon, Yiyoung, et al.
Publicado: (2021) -
Intestinal Lymphangiectasia
por: Monajemzadeh, M, et al.
Publicado: (2010) -
A Case of Primary Intestinal Lymphangiectasia
por: Won, Kyu Chang, et al.
Publicado: (1993)