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赖特综合征患者的淀粉样变——继发性还是巧合?用高锰酸钾进行鉴别。

Amyloid in a patient with Reiter's syndrome - secondary or coincidental? Differentiation with potassium permanganate.

作者信息

Mahowald M L, Pritzker M, Sarosi G A, Valls A A, Sumner H W

出版信息

J Rheumatol. 1980 Nov-Dec;7(6):903-6.

PMID:7205830
Abstract

A patient with Reiter's syndrome developed a pulmonary nodule composed of amyloid. Reiter's syndrome has been reported as 1 of the diseases associated with secondary systemic amyloidosis. Isolated nodular pulmonary amyloid has not been reported to become systemic. Potassium permanganate treatment of amyloid abolishes congo red stain affinity for amyloid of unknown origin found in secondary amyloidosis. However, the amyloid of immunoglobulin origin, characteristic of primary amyloid, is resistant to KMnO4. The amyloid deposit from our patient was resistant to KMnO4 which suggested that the pulmonary amyloid was a coincidental nodular amyloid deposit in the lung rather than secondary amyloidosis.

摘要

一名赖特综合征患者出现了一个由淀粉样蛋白构成的肺结节。赖特综合征已被报道为与继发性系统性淀粉样变性相关的疾病之一。孤立性结节性肺淀粉样变尚未有发展为系统性病变的报道。高锰酸钾处理淀粉样蛋白可消除刚果红对继发性淀粉样变性中来源不明的淀粉样蛋白的染色亲和力。然而,原发性淀粉样变性特有的免疫球蛋白来源的淀粉样蛋白对高锰酸钾有抗性。我们患者的淀粉样蛋白沉积物对高锰酸钾有抗性,这表明肺部淀粉样变是肺部偶然出现的结节性淀粉样蛋白沉积,而非继发性淀粉样变性。

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