Gonzalez-Crussi F, Hull M T, Grosfeld J L
Am Rev Respir Dis. 1976 Oct;114(4):689-98. doi: 10.1164/arrd.1976.114.4.689.
Electron microscopic examination of a lung biopsy obtained from a child in the active stage of idiopathic pulmonary hemosiderosis disclosed prominent changes in the basement membrane of alveolar capillaries. Review of the pertinent literature showed that a structural defect of lung capillary walls in this disease has been proposed in the past mainly on theoretic grounds but not adequately documented at the ultrastructural level. Concentric multilayering of pulmonary capillary basal lamina, one of the changes observed in our material, is a rare phenomenon in this location, although one that has been well described in extrapulmonary microcirculatory beds and is probably a nonspecific reaction to vascular injury. The conceptual difficulties attending a definition of idiopathic pulmonary hemosiderosis are breifly discussed.
对一名处于特发性肺含铁血黄素沉着症活动期的儿童进行肺活检的电子显微镜检查发现,肺泡毛细血管基底膜有明显变化。查阅相关文献表明,过去曾基于理论依据提出该病存在肺毛细血管壁结构缺陷,但在超微结构水平上缺乏充分的记录。肺毛细血管基膜的同心多层结构是我们观察到的变化之一,这种现象在该部位较为罕见,尽管在肺外微循环床中已有详细描述,可能是对血管损伤的一种非特异性反应。本文简要讨论了特发性肺含铁血黄素沉着症定义方面存在的概念性难题。