| Literature DB >> 28969188 |
Vijay Surampalli1, Srinath Ramaswamy1, Deepanjali Surendran2, Chanaveerappa Bammigatti3, Rathinam Palamalai Swaminathan4.
Abstract
Primary Intestinal Lymphangiectasia (PIL) is a rare disease of unknown aetiology which presents in the paediatric age group with anasarca, diarrhoea, hypoproteinaemia, lymphoedema and chylous effusions. Tuberculosis, filariasis, chest trauma, malignancies and haematological disorders usually contribute to most cases of secondary lymphangiectasia and chylous effusions. We hereby describe a case of PIL presenting with chylous effusions which remained undiagnosed for eight years.Entities:
Keywords: Fluid accumulation; Hypoproteinaemia; Idiopathic; Lymphatic dilatation; Milky lymph
Year: 2017 PMID: 28969188 PMCID: PMC5620829 DOI: 10.7860/JCDR/2017/29055.10522
Source DB: PubMed Journal: J Clin Diagn Res ISSN: 0973-709X