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特发性肺含铁血黄素沉着症的超微结构改变

Fine structural changes in idiopathic pulmonary haemosiderosis.

作者信息

Corrin B, Jagusch M, Dewar A, Tungekar M F, Davies D R, Warner J O, Turner-Warwick M, Empey D

机构信息

Cardiothoracic Institute, London, U.K.

出版信息

J Pathol. 1987 Nov;153(3):249-56. doi: 10.1002/path.1711530309.

Abstract

Lung biopsies from four children and two adults with idiopathic pulmonary haemosiderosis have been examined by transmission electron microscopy. No qualitative differences were identified between the children and the adults but the changes were more severe in the children. In each case the major damage involved the capillary endothelium and its basement membrane. Capillary endothelial swelling was very noticeable and in one case the endothelium was attenuated but gaps between endothelial cells were very difficult to find. Capillary narrowing and platelet aggregation were common. The capillary endothelial basement membrane showed focal thickening, particularly on the thick side of the air/blood barrier, but no electron dense deposits were identified. Degenerative changes in the alveolar epithelium were not so marked as those in the capillary endothelium and the epithelial basement membrane was normal except for haemosiderin deposition. Haemosiderin was also noted on elastin and within intra-alveolar macrophages. Other secondary changes included mild interstitial oedema and fibrosis. These findings indicate that the major site of damage is the alveolar capillary, but provide no evidence of the cause of the disease.

摘要

对4名儿童和2名患有特发性肺含铁血黄素沉着症的成人进行了肺活检,并通过透射电子显微镜进行了检查。儿童和成人之间未发现定性差异,但儿童的变化更为严重。在每种情况下,主要损伤累及毛细血管内皮及其基底膜。毛细血管内皮肿胀非常明显,在一个病例中内皮变薄,但很难找到内皮细胞之间的间隙。毛细血管狭窄和血小板聚集很常见。毛细血管内皮基底膜显示局灶性增厚,特别是在气/血屏障的厚侧,但未发现电子致密沉积物。肺泡上皮的退行性变化不如毛细血管内皮明显,除含铁血黄素沉积外,上皮基底膜正常。在弹性蛋白上和肺泡内巨噬细胞内也发现了含铁血黄素。其他继发性变化包括轻度间质水肿和纤维化。这些发现表明,主要损伤部位是肺泡毛细血管,但没有提供该疾病病因的证据。

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