| Literature DB >> 24449480 |
Laura Milazzo1, Anna Maria Peri, Lucia Lodi, Guido Gubertini, Anna Lisa Ridolfo, Spinello Antinori.
Abstract
Primary intestinal lymphangiectasia (PIL) is a protein-losing enteropathy characterized by tortuous and dilated lymph channels of the small bowel. The main symptoms are bilateral lower limb edema, serosal effusions, and vitamin D malabsorption resulting in osteoporosis. We report here a case of long-lasting misdiagnosed PIL with a peculiar liver picture, characterized by a very high stiffness value at transient elastography, which decreased with clinical improvement. The complex interplay between lymphatic and hepatic circulatory system is discussed.Entities:
Mesh:
Year: 2014 PMID: 24449480 DOI: 10.1002/hep.27025
Source DB: PubMed Journal: Hepatology ISSN: 0270-9139 Impact factor: 17.425