人纤维化肺泡炎的超微结构。

J J Coalson
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引用次数: 51

摘要

本文报告了37例经开肺活检诊断为纤维化肺泡炎的患者的超微结构表现。病变可分为毛细血管内皮及其基底膜、间质间隙及其纤维细胞成分、肺泡上皮及其基底膜。这些发现反映了肺细胞对损伤的不同反应。上皮细胞和内皮细胞群体中细胞再生和死亡的证据包括非典型上皮细胞增殖、毛细血管基底膜多层化、毛细血管管腔缩小和肺毛细血管明显的周细胞嵌套。在肺间质内,胶原和弹性纤维增生,但除此之外,还存在大量的肌成纤维细胞和平滑肌细胞。本研究未发现免疫复合物沉积的超微结构证据。纤维化性肺泡炎的形态学发现进一步支持了一个广泛的概念,即肺对各种损伤的反应方式相似,无论病因如何,都经历了共同的修复反应。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The ultrastructure of human fibrosing alveolitis.

This report describes the ultrastructural findings in 37 patients who underwent open lung biopsy which yielded diagnoses of fibrosing alveolitis. A spectrum of lesions are categorized for the capillary endothelium and its basement membrane, the interstitial space and its fibrocellular components, and the alveolar epithelium and its basement membrane. The findings typify the different pulmonary cellular reactions to injury. Evidence for cellular regeneration and death in both epithelial and endothelial cell populations include atypical epithelial cell proliferation, capillary basement membrane multilamination, decrease in capillary lumen size and prominent pericytic ensheathment of pulmonary capillaries. Within the interstitium of the lung, proliferation of collagen and elastic fibers are documented, but in addition, abundant myofibroblasts and smooth muscle cells are present. No ultrastructural evidence of immune complex deposition was found in this study. The morphologic findings of fibrosing alveolitis further support the widespread concept that the lung responds to various injuries in a similar manner and undergoes a common reparative response regardless of etiology.

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