Literature DB >> 11104932

[Familial Waldmann's disease].

P Le Bougeant1, X Delbrel, M Grenouillet, S Leou, F Djossou, J Beylot, M Lebras, M Longy-Boursier.   

Abstract

We report the observation of a mother and her daughter who presented edema, hypoprotidemia and lymphopenia due to protein-losing enteropathy. Radiological, endoscopic and histological investigations revealed the diagnosis of primary intestinal lymphangiectasis or Waldmann's disease. Dietary treatment with middle chained triglycerides was effective. Familial cases are rarely described.

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Year:  2000        PMID： 11104932

Source DB:  PubMed          Journal:  Ann Med Interne (Paris)        ISSN： 0003-410X


  5 in total

1.  Anaemia in Waldmann's disease: A rare presentation of a rare disease.

Authors:  Shahira A El-Etreby; Ahmed Y Altonbary; Mohamed El Sorogy; Wagdi Elkashef; Jehan A Mazroa; Monir H Bahgat
Journal:  World J Gastrointest Endosc       Date:  2015-05-16

2.  Digital clubbing in primary intestinal lymphangiectasia: a case report.

Authors:  Christian J Wiedermann; Michael Kob; Stefano Benvenuti; Rodolfo Carella; Lucio Lucchin; Lucia Piazzi; Fausto Chilovi; Guido Mazzoleni
Journal:  Wien Med Wochenschr       Date:  2010-08

Review 3.  Primary intestinal lymphangiectasia: Minireview.

Authors:  Sachin B Ingle; Chitra R Hinge Ingle
Journal:  World J Clin Cases       Date:  2014-10-16       Impact factor: 1.337

4.  Diagnostic dilemma in diagnosing rare cause of protein losing enteropathy: Waldmann's disease.

Authors:  Sarita Prajapati; Sujan Bohara; Gaurab Mainali; Samikshya Karki; Sharan Thapa; Nirjala Aryal
Journal:  Clin Case Rep       Date:  2022-06-21

Review 5.  Primary intestinal lymphangiectasia (Waldmann's disease).

Authors:  Stéphane Vignes; Jérôme Bellanger
Journal:  Orphanet J Rare Dis       Date:  2008-02-22       Impact factor: 4.123
  5 in total

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