Tuder R M, Groves B, Badesch D B, Voelkel N F
Department of Pathology, University of Colorado Health Sciences Center, Denver 80262.
Am J Pathol. 1994 Feb;144(2):275-85.
The plexiform lesion in primary pulmonary hypertension is a glomeruloid structure forming channels in branches of the pulmonary artery. These lesions have been considered an abnormal growth of modified smooth muscle cells. We present immunohistochemical evidence in 10 cases of plexogenic pulmonary hypertension that the plexiform channels and the concentric obliterative arteriopathy associated with these channels represent abnormal growth of factor VIII-related antigen-positive endothelial cells. In addition, these cells strongly expressed vimentin, a growth- and differentiation-related intermediate filament. Morphologically and immunohistochemically, the lesions resembled the neovascularization associated with the brain tumor glioblastoma multiform. Furthermore, we noted an exclusively perivascular inflammatory cell infiltrate (but no vasculitis) in seven of the 10 cases with plexogenic arteriopathy composed of T cells, B cells, and macrophages. Our findings indicate that the plexiform lesion may result from a deregulated growth of endothelial cells. The presence of perivascular inflammatory cells suggested that cytokines and growth factors may further influence the development of the plexiform lesion.
原发性肺动脉高压中的丛状病变是一种在肺动脉分支中形成通道的肾小球样结构。这些病变一直被认为是修饰的平滑肌细胞的异常生长。我们在10例致丛性肺动脉高压病例中提供了免疫组织化学证据,表明丛状通道以及与这些通道相关的同心性闭塞性动脉病代表了因子VIII相关抗原阳性内皮细胞的异常生长。此外,这些细胞强烈表达波形蛋白,一种与生长和分化相关的中间丝。在形态学和免疫组织化学上,这些病变类似于与多形性胶质母细胞瘤相关的新生血管形成。此外,在10例由T细胞、B细胞和巨噬细胞组成的致丛性动脉病病例中,我们注意到有7例仅存在血管周围炎性细胞浸润(但无血管炎)。我们的研究结果表明,丛状病变可能是由内皮细胞生长失控导致的。血管周围炎性细胞的存在表明细胞因子和生长因子可能进一步影响丛状病变的发展。