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具有非典型表现的乔布综合征。

Job's syndrome with an atypical presentation.

作者信息

Tasneem Abbas Ali, Sarfaraz Sabahat, Hassan Syed Mujahid, Luck Nasir Hassan, Anis Sabiha, Abbas Zaigham

机构信息

Department of Hepatogastroenterology, Aga Khan Hospital for Woman, Karimabad.

Department of Diagnostics and Immunology, Aga Khan Hospital for Woman, Karimabad.

出版信息

J Pak Med Assoc. 2013 Nov;63(11):1427-9.

Abstract

Hyper Immunoglobulin E syndrome also called Job's or Buckley Syndrome is a rare primary immunodeficiency disease characterized by elevated serum IgE levels (> 2000 IU/ml), recurrent infections and eosinophilia. Other features include coarse facies and non-immunologic abnormalities of the dentition, bones, vasculature and connective tissues. We are reporting a case of a twenty four years old male with coarse facies who presented with severe pallor and upper gastrointestinal bleeding. Investigations revealed markedly elevated serum IgE levels (11,800 IU/ml), severe anaemia, esophageoduodenal erosions, Helicobacter pylori (H. pylori) gastritis and oro-esophageal candidiasis.

摘要

高免疫球蛋白E综合征也称为乔布氏综合征或巴克利综合征,是一种罕见的原发性免疫缺陷病,其特征为血清IgE水平升高(>2000 IU/ml)、反复感染和嗜酸性粒细胞增多。其他特征包括面容粗糙以及牙齿、骨骼、血管和结缔组织的非免疫性异常。我们报告一例24岁男性患者,面容粗糙,伴有严重苍白和上消化道出血。检查发现血清IgE水平显著升高(11,800 IU/ml)、严重贫血、食管十二指肠糜烂、幽门螺杆菌胃炎和口腔食管念珠菌病。

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