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[β2微球蛋白淀粉样变性]

[Beta 2-microglobulin amyloidosis].

作者信息

Mazanec K, McClure J, Bartley C J, Newbould M J

机构信息

II. Patologicko-anmatomický ústav LF MU, Brno.

出版信息

Cesk Patol. 1992 Mar;28(1):42-7.

PMID:1596944
Abstract

A 35-year-old man who had been treated by hemodialysis for 15 years suffered from systemic amyloidosis. It was identified as a beta 2-microglobulin type according to immunohistochemistry. Extensive amyloid deposits were found in myocardium, cartilages of intervertebral discs and in carpal tunnel ligament. Less conspicuous deposits comprised blood vessels of lungs, liver, suprarenal glands, brain, and stroma of prostate gland, testicles, kidney, often combined with calcified foci.

摘要

一名接受血液透析治疗15年的35岁男性患有系统性淀粉样变性。根据免疫组织化学鉴定为β2-微球蛋白型。在心肌、椎间盘软骨和腕管韧带中发现广泛的淀粉样沉积物。不太明显的沉积物包括肺、肝、肾上腺、脑的血管以及前列腺、睾丸、肾的基质,常伴有钙化灶。

相似文献

1
[Beta 2-microglobulin amyloidosis].
Cesk Patol. 1992 Mar;28(1):42-7.
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Systemic amyloidosis of beta 2 microglobulin type.
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Systemic amyloidosis of beta 2-microglobulin type: a complication of long-term haemodialysis.
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