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人类过敏性肺炎。18例肺活检的光镜和电镜研究。

Hypersensitivity pneumonitis in man. Light- and electron-microscopic studies of 18 lung biopsies.

作者信息

Kawanami O, Basset F, Barrios R, Lacronique J G, Ferrans V J, Crystal R G

出版信息

Am J Pathol. 1983 Mar;110(3):275-89.

Abstract

Light- and electron-microscopic changes produced by hypersensitivity pneumonitis were analyzed in open lung biopsies taken from 18 patients with chronic forms of the disease. The main changes observed were: alveolitis (both luminal and mural), granulomas, intraalveolar buds, and interstitial fibrosis. The cells infiltrating the alveolar walls were mainly lymphocytes. Occasionally these lymphocytes presented irregularities in the contours of the nuclear membranes and resembled Sézary cells. In one patient, a few lymphocytes were found that resembled "hand-mirror" cells. Intraalveolar macrophages often had a foamy appearance. Granulomas, present in two-thirds of the patients, differed in several respects from those in sarcoidosis: they were smaller, more loosely arranged, and poorly limited; they had a higher content of lymphocytes; and they were located more frequently in alveolar tissue than in the vicinity of bronchioles and vessels. Intraalveolar buds, also present in about two thirds of the patients, were composed mainly of fibroblasts, myofibroblasts, and macrophages in a loose connective tissue that was rich in proteoglycan material. Capillaries and epithelial cells were rarely seen in buds. Alveolar buds appear to develop by a process of disruption of the epithelial lining layer, due to alveolitis, followed by intraalveolar exudation and by subsequent intraalveolar migration of connective tissue cells interacting with macrophages. Severe fibrotic and alveolar epithelial changes were observed in four patients; milder changes were frequent in most other patients. It is concluded that hypersensitivity pneumonitis usually has distinctive morphologic features; these may help to distinguish the resultant pulmonary fibrosis from that due to other causes.

摘要

对18例慢性超敏性肺炎患者的开胸肺活检组织进行光镜和电镜分析,以观察其病变情况。主要观察到的变化有:肺泡炎(包括管腔和壁层)、肉芽肿、肺泡内芽肿和间质纤维化。浸润肺泡壁的细胞主要是淋巴细胞。偶尔,这些淋巴细胞的核膜轮廓不规则,类似Sezary细胞。在1例患者中,发现少数类似“手镜”细胞的淋巴细胞。肺泡内巨噬细胞常呈泡沫状外观。三分之二的患者存在肉芽肿,其在几个方面与结节病中的肉芽肿不同:它们较小,排列更松散,界限不清;淋巴细胞含量较高;且更常见于肺泡组织而非细支气管和血管附近。约三分之二的患者也存在肺泡内芽肿,主要由成纤维细胞、肌成纤维细胞和巨噬细胞组成,位于富含蛋白聚糖物质的疏松结缔组织中。芽肿内很少见到毛细血管和上皮细胞。肺泡内芽肿似乎是由于肺泡炎导致上皮衬里层破坏,随后肺泡内渗出,结缔组织细胞与巨噬细胞相互作用并在肺泡内迁移而形成的。4例患者观察到严重的纤维化和肺泡上皮改变;大多数其他患者则常见较轻的改变。结论是,超敏性肺炎通常具有独特的形态学特征;这些特征可能有助于将由此导致的肺纤维化与其他原因引起的肺纤维化区分开来。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1428/1916173/8bb4247152bb/amjpathol00198-0037-a.jpg

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