原发性全身性AL淀粉样变性

[Primary generalized AL amyloidosis].

作者信息

Kogan E A, Saltykov B B, Atanov P V

机构信息

I.M. Sechenov First Moscow State University (Sechenov University) of the Ministry of Health of Russia, Moscow, Russia.

出版信息

Arkh Patol. 2021;83(1):31-34. doi: 10.17116/patol20218301131.

DOI:10.17116/patol20218301131

PMID:33512125

Abstract

The paper describes an autopsy observation of a 71-year-old male with primary generalized AL amyloidosis lasting about 4 months after its manifestation to the onset of death from hepatic and renal failure. Total damage to the liver and spleen, as well as amyloid deposits in the kidneys, adrenal glands, and pancreas were noted.

摘要

该论文描述了一名71岁男性原发性全身性AL淀粉样变性的尸检观察结果，从发病到因肝肾功能衰竭死亡持续约4个月。观察到肝脏和脾脏完全受损，以及肾脏、肾上腺和胰腺中有淀粉样沉积物。