[Amyloidosis and its bronchopulmonary localizations. Apropos of 3 cases].

Le Poumon et le coeur Pub Date : 1983-01-01
M Peuchmaur, F Capron, J L Dessirier, O de Fenoyl, O Roque d'Orbcastel, J Rochemaure
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Abstract

Amyloidosis of the lower respiratory tract is a rare condition. We report three new cases and we review the literature. Tracheobronchial amyloidosis is the most frequent form. The diagnostic is made by fiberoscopy and biopsies with a risk of bleeding. Our patients were usually treated with intermittent bronchoscopic resections. In one of the three cases reported, desobstruction of the large airway was performed with laser. Nodular pulmonary amyloidosis is usually asymptomatic, and surgical resection results in cure in all cases. Diffuse pulmonary amyloidosis is very unusual and fatal.

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淀粉样变性及其支气管肺定位。(3例)。
下呼吸道淀粉样变是一种罕见的疾病。我们报告了三个新病例,并回顾了文献。气管支气管淀粉样变是最常见的形式。诊断是通过纤维镜检查和有出血风险的活组织检查做出的。我们的病人通常采用间歇性支气管镜切除治疗。在报告的三个病例中,有一个用激光对大气道进行了疏通。结节性肺淀粉样变通常无症状,手术切除可治愈所有病例。弥漫性肺淀粉样变是一种罕见且致命的疾病。
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