Shimada Yoshitaka, Takahashi Yoshihito, Iguchi Hiroyoshi, Yamazaki Hitoshi, Tsunoda Hidekazu, Watanabe Masaaki, Oda Masaya, Yokomori Hiroaki
J Med Case Rep. 2013 May 28;7:139. doi: 10.1186/1752-1947-7-139.
Liver cavernous hemangioma is the most common noncystic hepatic lesion, and a hemangioma that undergoes degeneration and fibrous replacement is called a hepatic sclerosed hemangioma.
A 63-year-old Japanese man was admitted for detailed investigation of a liver tumor. Tumor markers carcinoembryonic antigen, alpha-fetoprotein, and CA19-9 levels in the peripheral blood were not elevated at any time. Plain computed tomography showed an approximately 1.5 cm low density mass in the periphery of segment 8, which was marginally enhanced on contrast-enhanced dynamic computed tomography. On magnetic resonance imaging, the tumor was hypointense on T1-weighted image and hyperintense on T2-weighted image. The tumor was suspected to be an atypical hemangioma, metastatic, hepatocellular carcinoma, or cholangiocellular carcinoma. Segmental hepatectomy was performed. Histological examination of the resected tumor specimen revealed a sclerosed hemangioma with marked hyalinization and sparse stromal fibrosis. Immunochemically, the tumor cells were positive for CD34 and alpha smooth muscle actin. Electron microscopically, the residual hemangioma consisted of numerous caveolae and vesicles in endothelial cells in irregular shapes and sizes. Immunostaining for caveolin-1 showed decreased or no caveolin-1 reactivity in the hyalinized lesions of the sclerosed hemangioma, but abundant caveolin-1 reactivity in the residual cavernous hemangioma. Of interest, computed tomography images of the tumor obtained 10 years earlier at our hospital depicted a 3 cm typical cavernous hemangioma.
Hepatic sclerosed hemangioma is a rare condition. Comparison of radiological findings of the lesion over a period of 10 years was valuable in providing insight for the evolutional process from liver cavernous hemangioma to hepatic sclerosed hemangioma.
肝海绵状血管瘤是最常见的非囊性肝脏病变,发生退变和纤维替代的血管瘤称为肝硬化性血管瘤。
一名63岁的日本男性因肝脏肿瘤的详细检查入院。外周血中的肿瘤标志物癌胚抗原、甲胎蛋白和CA19-9水平在任何时候均未升高。平扫计算机断层扫描显示8段外周有一个约1.5 cm的低密度肿块,在动态增强计算机断层扫描中边缘强化。在磁共振成像上,肿瘤在T1加权图像上呈低信号,在T2加权图像上呈高信号。该肿瘤疑似为非典型血管瘤、转移性肝癌或胆管细胞癌。遂行肝段切除术。对切除的肿瘤标本进行组织学检查,发现为硬化性血管瘤,伴有明显的玻璃样变和稀疏的间质纤维化。免疫组化显示肿瘤细胞CD34和α平滑肌肌动蛋白呈阳性。电子显微镜下,残留的血管瘤由内皮细胞中众多大小和形状不规则的小窝和囊泡组成。对小窝蛋白-1的免疫染色显示,硬化性血管瘤的玻璃样变病变中小窝蛋白-1反应性降低或无反应,但残留的海绵状血管瘤中存在丰富的小窝蛋白-1反应性。有趣的是,10年前在我院获得的该肿瘤的计算机断层扫描图像显示为一个3 cm的典型海绵状血管瘤。
肝硬化性血管瘤是一种罕见疾病。对该病变10年期间的影像学表现进行比较,对于了解从肝海绵状血管瘤到肝硬化性血管瘤的演变过程具有重要价值。