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系统性淀粉样变性和低丙种球蛋白血症。

Systemic amyloidosis and hypogammaglobulinemia.

作者信息

Gaffney E F, Lee J C

出版信息

Arch Pathol Lab Med. 1978 Nov;102(11):558-9.

PMID:581446
Abstract

Small deposits of amyloid were found at autopsy in the kidneys, liver, spleen, and blood vessels of the intestines of a patient known to have primary acquired hypogammaglobulinemia. Previously described cases of hypogammaglobulinemia-associated amyloid are reviewed and possible pathogenetic mechanisms are discussed. The pathogenesis of amyloidosis in this patient is not known.

摘要

在一名已知患有原发性获得性低丙种球蛋白血症患者的尸检中,发现其肾脏、肝脏、脾脏以及肠血管中有小的淀粉样蛋白沉积物。回顾了先前描述的与低丙种球蛋白血症相关的淀粉样变性病例,并讨论了可能的发病机制。该患者淀粉样变性的发病机制尚不清楚。

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