Lai Ri-quan, Feng Xiao-dong, Gu Ying-ying, Lai Huang-wen, Liu Fang, Tian Ye, Wang Zhou-cai, Zhang Wei, Chen Guo-qin, Yang Chuan-hong, Yang Tong
Department of Pathology, General Hospital of Guangzhou Command, Guangzhou 510010, China.
Zhonghua Bing Li Xue Za Zhi. 2004 Aug;33(4):354-7.
To evaluate the progression in morphologic changes of lungs in SARS patients.
Four cases of SARS with lung tissue samples available (including one for ultrastructural examination) were enrolled into the study. Histochemical study for VG, Masson, reticulin, orcein, PAS, sirius red stains and immunohistochemical study for vimentin, desmin, smooth muscle actin, HHF-35, CD34, F8, collagen types I and III were also performed.
According to the morphologic changes, lung lesions in SARS were subcategorized into 3 phases: acute exudative inflammation, fibrous proliferation and the final fibrotic stage. Two cases belonged to the acute exudative phase, in which the course was less than 20 days. The principal lesions consisted of acute alveolar exudative inflammation, hyperplasia of alveolar epithelium, necrosis, alveolar hyaline membrane formation, alveolar desquamation and focal fibroplasia. The acute exudative protein was PAS-positive. There was an increase in reticulin fiber formation. The reactive fibroblasts were highlighted by desmin and vimentin. One case belonged to the fibroproliferative stage, in which the course was around 25 days. Major lesions included proliferative interstitial pneumonia with early pulmonary fibrosis. There was also evidence of organizing pneumonia, with an increase in reticulin fiber formation, which had a glomeruloid appearance on special stain. The mesenchymal cells showed either myofibroblastic (which expressed desmin, HHF-35, smooth muscle actin and vimentin) or fibroblastic (which expressed vimentin only) differentiation. Fibroelastosis and fibroplasia was also noted. The remaining case belonged to the fibrotic stage, in which the course was around 75 days. The main features included diffuse fibrosis and honeycomb change, which were highlighted by sirius red stain. Immunohistochemistry showed mainly types I and IV collagen fibers. In all lesions, there was also an increase of number of CD68-positive macrophages.
The morphologic progression in lungs of SARS patients is characterized by the development of increased fibrosis. The primitive mesenchymal cells, hyperplastic alveolar epithelial cells and macrophages play an important role in the pathogenesis.
评估严重急性呼吸综合征(SARS)患者肺部形态学变化的进展情况。
选取4例有肺组织样本的SARS患者(其中1例用于超微结构检查)纳入本研究。还进行了维多利亚蓝(VG)、马松(Masson)、网状纤维、地衣红、过碘酸雪夫(PAS)、天狼星红染色的组织化学研究以及波形蛋白、结蛋白、平滑肌肌动蛋白、HHF-35、CD34、F8、Ⅰ型和Ⅲ型胶原的免疫组织化学研究。
根据形态学变化,SARS肺部病变分为3期:急性渗出性炎症期、纤维组织增生期和最终的纤维化期。2例属于急性渗出期,病程小于20天。主要病变包括急性肺泡渗出性炎症、肺泡上皮增生、坏死、肺泡透明膜形成、肺泡脱屑和局灶性纤维组织增生。急性渗出蛋白PAS染色呈阳性。网状纤维形成增加。结蛋白和波形蛋白突出显示反应性成纤维细胞。1例属于纤维组织增生期,病程约25天。主要病变包括增生性间质性肺炎伴早期肺纤维化。也有组织性肺炎的证据,网状纤维形成增加,特殊染色显示呈肾小球样外观。间充质细胞表现为肌成纤维细胞(表达结蛋白、HHF-35、平滑肌肌动蛋白和波形蛋白)或成纤维细胞(仅表达波形蛋白)分化。还可见纤维弹性组织增生和纤维组织增生。其余1例属于纤维化期,病程约75天。主要特征包括弥漫性纤维化和蜂窝状改变,天狼星红染色突出显示这些特征。免疫组织化学显示主要为Ⅰ型和Ⅳ型胶原纤维。在所有病变中,CD68阳性巨噬细胞数量也增加。
SARS患者肺部形态学进展的特征是纤维化增加。原始间充质细胞、增生的肺泡上皮细胞和巨噬细胞在发病机制中起重要作用。