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[一例以大量心包积液为表现的亨内坎综合征病例]

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

作者信息

Nişli Kemal, Oner Naci, Kayserili Hülya, Ertuğrul Türkan

机构信息

Istanbul Universitesi Istanbul Tip Fakültesi, Cocuk Sağliği ve Hastaliklari Anabilim Dali, Istanbul, Turkey.

出版信息

Turk Kardiyol Dern Ars. 2008 Jul;36(5):325-8.

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.

摘要

亨内坎综合征是一种常染色体隐性疾病,其特征为肠道淋巴管扩张,并伴有四肢、生殖器及面部的严重淋巴水肿以及学习困难。一名38个月大的男孩因呼吸困难入院。他有与亨内坎综合征相符的面部异常及包皮增生。淋巴管造影显示左眼和右脚存在淋巴水肿。远距放射照相显示心脏扩大,超声心动图显示大量心包积液。他首先接受了心包穿刺术以清除心包积液,但积液复发时需要进行心包置管引流。在第五天,由于引流量显著减少,引流管被拔除。

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