| Literature DB >> 11044930 |
M Keberle1, H Mörk, M Jenett, D Hahn, M Scheurlen.
Abstract
Noonan's syndrome is a rare congenital disorder that may be associated with abnormalities in the lymphatic drainage. In this case of a 21-year-old man CT after bipedal lymphangiography confirmed the diagnosis of intestinal lymphangiectasy causing protein-losing enteropathy in Noonan's syndrome by showing contrast-enhanced abnormal lymphatic vessels in the mesentery and the intestinal wall. Because of the benefit of diet in case of intestinal involvement, we recommend a thorough documentation of the lymphatic drainage with lymphangiography followed by CT, if clinical signs of lymphatic dysplasia, such as pleural effusions, lymphedema, or hypoproteinemia are present.Entities:
Mesh:
Year: 2000 PMID: 11044930 DOI: 10.1007/s003300000384
Source DB: PubMed Journal: Eur Radiol ISSN: 0938-7994 Impact factor: 5.315