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伴有继发性淀粉样变性发展的慢性家族性地中海热。

Chronic familial Mediterranean fever with development of secondary amyloidosis.

作者信息

Larrimore Christopher

出版信息

Clin Lab Sci. 2011 Winter;24(1):2-7.

Abstract

A 20-year-old Turkish male presented with fever, abdominal pain, and systemic lethargy. His clinical history revealed symptoms to be self-limiting but reoccurring over the past six months. Blood and urine specimens collected indicated renal amyloidosis. A kidney CT image indicated kidney inflammation. He was diagnosed with Familial Mediterranean Fever with the development of secondary amyloidosis and treated with colchicine.

摘要

一名20岁的土耳其男性出现发热、腹痛和全身乏力症状。他的临床病史显示这些症状具有自限性,但在过去六个月中反复出现。采集的血液和尿液样本显示患有肾淀粉样变性。肾脏CT图像显示肾脏炎症。他被诊断为家族性地中海热并伴有继发性淀粉样变性,接受了秋水仙碱治疗。

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