Literature DB >> 16586269

[Congenital intestinal lymphangiectasia: a rare differential diagnosis in hypoproteinemia in infants].

A Möller1, H Kalhoff, T Reuter, N Friedrichs, N Wagner.   

Abstract

BACKGROUND: Congenital intestinal lymphangiectasia is a rare disease in childhood, which may already cause protein-losing enteropathy in newborns. PATIENT, METHODS AND
RESULTS: This is a case report of an infant with generalized edema and protein-losing enteropathy, in whom intestinal lymphangiectasia was diagnosed at the age of two months. Following repetitive intravenous albumin und gamma globulin infusions, the elimination of long-chain fats from the diet and the substitution with medium-chain triglycerides (MCT) led to an improvement of the protein-losing enteropathy.
CONCLUSION: In newborns with low level of serum protein and edema protein-losing enteropathy caused by congenital lymphangiectasia might be considered as a differential diagnosis.

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Year:  2006        PMID: 16586269     DOI: 10.1055/s-2006-921454

Source DB:  PubMed          Journal:  Klin Padiatr        ISSN: 0300-8630            Impact factor:   1.349


  2 in total

1.  Clinical outcome of nutrition-oriented intervention for primary intestinal lymphangiectasia.

Authors:  Qing-Ya Tang; Jie Wen; Jiang Wu; Ying Wang; Wei Cai
Journal:  World J Pediatr       Date:  2010-12-30       Impact factor: 2.764

Review 2.  Primary intestinal lymphangiectasia: four case reports and a review of the literature.

Authors:  Jie Wen; Qingya Tang; Jiang Wu; Ying Wang; Wei Cai
Journal:  Dig Dis Sci       Date:  2010-03-03       Impact factor: 3.199

  2 in total

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