弥漫性肺淀粉样变性。2例与瓦尔登斯特罗姆病相关的病例]。

Le Poumon et le coeur Pub Date : 1982-01-01
M Martin, P Peltier, P Le Lann, R Garand, F Gaillard
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引用次数: 0

摘要

弥漫性肺淀粉样变性在系统性淀粉样变性中很少报道。我们报告了两例Waldenström巨球蛋白血症患者,其中弥漫性间质综合征显示肺淀粉样变性,但没有严重的功能损害。肺淀粉样沉积在解剖学上是常见的,通常与心脏淀粉样变性有关。在弥漫性间质型的诊断中,尤其是原发性淀粉样变性或球蛋白异常患者,必须更频繁地使用它们。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[Diffuse pulmonary amylosis. Apropos of 2 cases associated with Waldenstrom's disease].

Diffuse pulmonary amyloidosis is rarely reported in systemic amyloidosis. We report two patients with Waldenström's macroglobulinemia in whom pulmonary amyloidosis was revealed by a diffuse interstitial syndrome without severe functional impairment. Amyloid pulmonary deposits are anatomically frequent and are often associated with cardiac amyloidosis. They must be evoked more frequently in the diagnosis of diffuse interstitial patterns, particularly in patients with primary amyloidosis or dysglobulinemia.

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