| Literature DB >> 14676733 |
F Greco1, G Piccolo, A Sorge, P Pavone, T Triglia, M Spina, G Sorge.
Abstract
Primary intestinal lymphangiectasia is a rare disorder, characterized by hypoproteinemia due to obstruction of the intestinal lymphatic vessels and loss of lymph fluid in the gastrointestinal tract. The case of a 3-month old patient with protein-losing enteropathy due to a primitive intestinal lymphangiectasia diagnosed with duodenal histology is reported. The adapted formula was replaced by a formula enriched with medium-chain triglycerides (MCT) and the patient presented a clinical and biochemical improvement. The importance of an early diagnosis and the efficacy of treatment with MCT is stressed.Entities:
Mesh:
Year: 2003 PMID: 14676733
Source DB: PubMed Journal: Minerva Pediatr ISSN: 0026-4946 Impact factor: 1.312