Inoue Harumi, Miyazaki Yuji, Kikuchi Kentaro, Fujinami Masahiro, Yoshida Noriaki, Ide Fumio, Sakashita Hideaki, Kusama Kaoru
Department of Diagnostic and Therapeutic Sciences, Meikai University School of Dentistry, Sakado, Japan.
J Oral Sci. 2011 Dec;53(4):475-80. doi: 10.2334/josnusd.53.475.
To examine the pathogenesis of intravascular papillary endothelial hyperplasia (IPEH), a relatively uncommon benign, non-neoplastic vascular lesion, clinicopathological and immunohistochemical studies were performed. Paraffin-embedded tissue specimens of 78 vascular lesions were examined histologically, and 9 cases of IPEH were investigated immunohistochemically using antibodies against CD34, vimentin, factor VIII antigen, α-smooth muscle actin (α-SMA), podoplanin, CD105, and ki-67 antigen. A thrombus or ulcer was found near the sites of all IPEH specimens. Histologic examination revealed papillary proliferated endothelial cells located toward the lumen of enlarged blood vessels. Immunohistochemistry showed that CD34, α-SMA, and factor VIII antigen were positive in lining endothelial cells. Vimentin was positive in the mesenchymal components. Immunohistochemical staining for podoplanin and CD105 was partially positive. Labeling index was 4.7 to 9.2 in ki-67-positive cases. IPEH is believed to result from reactive proliferation of blood endothelial cells that is caused by an abnormal process of organization in thrombosed blood vessels. The pathogenesis of IPEH might be related to inflammation or mechanical stimulus such as irritation.
为研究血管内乳头状内皮增生(IPEH)这一相对少见的良性非肿瘤性血管病变的发病机制,我们进行了临床病理及免疫组化研究。对78例血管病变的石蜡包埋组织标本进行了组织学检查,并使用抗CD34、波形蛋白、因子VIII抗原、α平滑肌肌动蛋白(α-SMA)、足板蛋白、CD105和ki-67抗原的抗体对9例IPEH进行了免疫组化研究。在所有IPEH标本部位附近均发现血栓或溃疡。组织学检查显示,乳头状增生的内皮细胞朝向扩张血管的管腔。免疫组化显示,CD34、α-SMA和因子VIII抗原在内衬内皮细胞中呈阳性。波形蛋白在间充质成分中呈阳性。足板蛋白和CD105的免疫组化染色部分呈阳性。ki-67阳性病例的标记指数为4.7至9.2。IPEH被认为是由血栓形成血管中异常机化过程导致的血液内皮细胞反应性增生所致。IPEH的发病机制可能与炎症或机械刺激如刺激有关。