自发性气胸患者大泡和大泡中异常弹性纤维的组织发生:超微结构和免疫组织化学研究。

S Haraguchi, Y Fukuda
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引用次数: 10

摘要

对自发性气胸15个大泡和17个大泡的弹性纤维进行了电镜和光镜及电镜免疫组化,并对弹性蛋白和α 1-抗胰蛋白酶进行了检测。气泡形成与局灶性组织性肺泡有关,大泡形成与肺气肿有关。水泡和大疱均有异常的弹性纤维。在超微结构上,大泡和大泡的异常弹性纤维由堆积的粗纤维和细纤维组成。积累的厚弹性纤维呈空泡状变化和电子致密颗粒状沉积,并与螺旋状胶原原纤维有关。这些厚弹性纤维与抗弹性蛋白抗体反应均匀,也与抗α - 1-抗胰蛋白酶抗体反应。它们被认为是退化的弹性纤维。积累的细弹性纤维由成束的微纤维和粒状无定形成分组成,它们与抗弹性蛋白和抗α 1-抗胰蛋白酶抗体发生反应。这些细小的弹性纤维被认为是在组织过程中新形成的,也可能是降解的。提示大泡和大泡弹性纤维的降解是由于弹性蛋白酶和α 1-抗胰蛋白酶之间的不平衡所致。
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Histogenesis of abnormal elastic fibers in blebs and bullae of patients with spontaneous pneumothorax: ultrastructural and immunohistochemical studies.

Elastic fibers in 15 blebs and 17 bullae with spontaneous pneumothorax were studied by means of electron microscopy and light and electron microscopic immunohistochemistry for elastin and alpha 1-antitrypsin. Blebs were formed in association with focal organized alveoli, and bullae were formed in association with pulmonary emphysema. Both blebs and bullae had abnormal elastic fibers. Ultrastructurally, abnormal elastic fibers of blebs and bullae consisted of accumulated thick and fine fibers. Accumulated thick elastic fibers showed vacuolar changes and electron-dense granular deposits, and they were associated with spiraling collagen fibrils. These thick elastic fibers reacted evenly with antielastin antibody and also reacted with anti-alpha 1-antitrypsin antibody. They are thought to be degraded elastic fibers. Accumulated fine elastic fibers consisted of bundles of microfibrils and granular amorphous components, and they reacted with anti-elastin and anti-alpha 1-antitrypsin antibody. These fine elastic fibers are thought to be not only newly formed in the process of organization but also degraded. It is suggested that elastic fibers of blebs and bullae are degraded due to an imbalance between elastase and alpha 1-antitrypsin.

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