Literature DB >> 24449480

Intestinal lymphangiectasia and reversible high liver stiffness.

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.
© 2014 by the American Association for the Study of Liver Diseases.

Entities:  

Mesh:

Year:  2014        PMID: 24449480     DOI: 10.1002/hep.27025

Source DB:  PubMed          Journal:  Hepatology        ISSN: 0270-9139            Impact factor:   17.425


  3 in total

1.  Liver fibrosis in primary intestinal lymphangiectasia: An undervalued topic.

Authors:  Raffaele Licinio; Mariabeatrice Principi; Enzo Ierardi; Alfredo Di Leo
Journal:  World J Hepatol       Date:  2014-09-27

Review 2.  Lymphatic dysfunction in advanced cirrhosis: Contextual perspective and clinical implications.

Authors:  Ramesh Kumar; Utpal Anand; Rajeev Nayan Priyadarshi
Journal:  World J Hepatol       Date:  2021-03-27

Review 3.  Primary intestinal lymphangiectasia in an adult patient: A case report and review of literature.

Authors:  Rudolf Huber; Georg Semmler; Alexander Mayr; Felix Offner; Christian Datz
Journal:  World J Gastroenterol       Date:  2020-12-08       Impact factor: 5.742

  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.