Barbareschi M, Ferrero S, Aldovini D, Leonardi E, Colombetti V, Carboni N, Mariscotti C
3rd Chair of Morbid Anatomy and Histopathology, School of Medicine, State University of Milan, Milano, Italy.
Histol Histopathol. 1990 Apr;5(2):205-11.
Inflammatory pseudotumour of the lung (I.P.) is a quite rare benign lesion, variously named by different authors. In the present report four new cases of I.P. are presented and immunohistochemically studied with a panel of antibodies. Microscopically, the most prominent histological features were the presence of interlacing bundles of elongated histiocytic-like cells, plasma cell aggregates and lymphoid follicles. Immunohistochemistry showed that plasma cells are polyclonal. The spindle cells were negative for desmin, cytokeratins, lysozyme and S-100 and immunoreactive for alpha-1-antichymotrypsin, vimentin and for smooth-muscle alpha-actin. Actin and desmin, were clearly evident in the vessels' smooth muscle layers, highlighting the angioinvasive behaviour of the lesions. Our data are in keeping with literature suggesting that I.P. is due to a mixed histiocytic-myofibroblastic-reactive proliferation and support the inflammatory nature of IP.
肺炎性假瘤(I.P.)是一种相当罕见的良性病变,不同作者对其有不同命名。在本报告中,呈现了4例肺炎性假瘤新病例,并使用一组抗体进行了免疫组织化学研究。显微镜下,最显著的组织学特征是存在交织的细长组织细胞样细胞束、浆细胞聚集物和淋巴滤泡。免疫组织化学显示浆细胞是多克隆性的。梭形细胞结蛋白、细胞角蛋白、溶菌酶和S-100呈阴性,而对α-1抗糜蛋白酶、波形蛋白和平滑肌α-肌动蛋白呈免疫反应性。肌动蛋白和结蛋白在血管平滑肌层中明显可见,突出了病变的血管侵袭性行为。我们的数据与文献一致,表明肺炎性假瘤是由于组织细胞-肌成纤维细胞混合性反应性增生所致,并支持其炎症性质。