Literature DB >> 18984984

[A case of Hennekam syndrome presenting with massive pericardial effusion].

Kemal Nişli1, Naci Oner, Hülya Kayserili, Türkan Ertuğrul.   

Abstract

Hennekam syndrome is an autosomal recessive disease characterized by intestinal lymphangiectasia accompanied by severe lymphedema of the limbs, genitalia, and face, and learning difficulties. A 38-month-old boy was admitted with breathing difficulty. He had facial abnormalities and preputial hyperplasia consistent with Hennekam syndrome. Lymphangiography showed lymphedema in the left eye and right foot. Teleradiography showed cardiomegaly and echocardiography showed massive pericardial effusion. He first underwent pericardiocentesis for the removal of pericardial effusion, but pericardial tube drainage was required upon recurrence of effusion. On the fifth day, the drain was removed because of significant decrease in the drainage.

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Year:  2008        PMID: 18984984

Source DB:  PubMed          Journal:  Turk Kardiyol Dern Ars        ISSN: 1016-5169


  2 in total

1.  A Rare Cause of Chylothorax: Hennekam Syndrome.

Authors:  Hayriye Bektaş; Yılmaz Bülbül; Savaş Özsu; Tevfik Özlü
Journal:  Turk Thorac J       Date:  2014-11-05

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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