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原发性狼疮相关蛋白丢失性肠病

Primary lupus-associated protein-losing enteropathy.

作者信息

Sunheimer R L, Finck C, Mortazavi S, McMahon C, Pincus M R

机构信息

Department of Pathology, SUNY Health Science Center, Syracuse 13210.

出版信息

Ann Clin Lab Sci. 1994 May-Jun;24(3):239-42.

PMID:8048795
Abstract

A 79-year-old native American female with a history of diabetes mellitus, but no history of hepatic or renal disease, presented with anasarca and hypoalbuminemia. Laboratory tests for fecal alpha 1-antitrypsin and an indium III-labeled plasma transferrin nuclear scan revealed a protein-losing enteropathy. A serological test was positive for antinuclear antibody in a titer of 1:1250 with a homogeneous pattern. This finding combined with low normal serum complement levels suggested the diagnosis of systemic lupus erythematosus (SLE). This case is unusual in that protein-losing enteropathy was the only presenting symptoms. The late onset of this disease is also unusual.

摘要

一名79岁的美国原住民女性,有糖尿病史,但无肝脏或肾脏疾病史,出现全身水肿和低白蛋白血症。粪便α1-抗胰蛋白酶检测及铟III标记的血浆转铁蛋白核素扫描显示为蛋白丢失性肠病。血清学检测抗核抗体阳性,滴度为1:1250,呈均质型。这一发现结合血清补体水平略低提示系统性红斑狼疮(SLE)的诊断。该病例不同寻常之处在于蛋白丢失性肠病是唯一的首发症状。这种疾病的迟发性也不常见。

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