Yugawa Kyohei, Yoshizumi Tomoharu, Harada Noboru, Motomura Takashi, Harimoto Norifumi, Itoh Shinji, Ikegami Toru, Soejima Yuji, Maehara Yoshihiko
Department of Surgery and Science, Graduate School of Medical Sciences, Kyushu University, Maidashi 3-1-1, Higashi-ku, Fukuoka, 812-8582, Japan.
Department of Hepatobiliary and Pancreatic Surgery, Gunma University, Showa-machi 3-39-22, Maebashi-shi, Gunma, 371-85111, Japan.
Surg Case Rep. 2018 Jun 19;4(1):60. doi: 10.1186/s40792-018-0468-6.
Hepatic sclerosing hemangioma, a very rare benign tumor, is characterized by fibrosis and hyalinization occurring in association with degeneration of a hepatic cavernous hemangioma. Such atypical hemangiomas can be diagnosed incorrectly as primary or metastatic malignancies based on imaging characteristics. We present herein a rare case of giant and multiple hepatic sclerosing hemangiomas that are difficult to differentiate from hepatic malignancies and review the relevant literature.
The patient was a 48-year-old male who was found to have multiple hepatic tumors and a giant tumor (67 × 53 mm) superior to the inferior vena cave by an abdominal ultrasonography during a routine medical examination. The patient was referred to our hospital for further evaluations and diagnosis of the multiple hepatic tumors. Dynamic CT showed low-density tumors in the delayed phase suggestive of membrane-covered lesions. EOB-MRI demonstrated a mass with low-signal intensity mass on T1-weighted images and areas of high-signal intensity on T2-weighted images and a hypointense mass in the hepatobiliary phase, which showed high intensity on DWI-based ADC map. FDG-PET showed no accumulation of [F]-FDG. A provisional diagnosis of multiple scirrhous hepatocellular carcinomas was made on the basis of these imaging studies, and caudate lobectomy of the liver and partial hepatectomy of S2 and S6 were performed. Histopathological examination showed that the tumors were composed of various sized irregularly dilated vessels with some blood thrombi, inflammatory cell infiltration, fibrous and hyalinized sclerotic or myxomatous stroma, resulting in a diagnosis of multiple hepatic sclerosing hemangiomas.
Differentiation of multiple sclerosing hemangiomas from other hepatic malignant tumors, such as intrahepatic cholangiocarcinoma, metastatic liver cancer, and scirrhous hepatocellular carcinoma characterized by abundant fibrous stroma, is difficult because the radiological findings are very similar. Inclusion of hepatic sclerosing hemangioma in the differential diagnosis of multiple liver tumors could enable optimal management; this possibility is important to consider before planning invasive therapies.
肝硬化性血管瘤是一种极为罕见的良性肿瘤,其特征为肝海绵状血管瘤退变时伴有纤维化和玻璃样变。基于影像学特征,此类非典型血管瘤可能被误诊为原发性或转移性恶性肿瘤。本文报告1例罕见的巨大多发性肝硬化性血管瘤病例,该病例难以与肝恶性肿瘤相鉴别,并对相关文献进行复习。
患者为48岁男性,在常规体检中经腹部超声检查发现肝脏有多发性肿瘤,下腔静脉上方有一巨大肿瘤(67×53mm)。患者因肝脏多发性肿瘤被转诊至我院进一步评估和诊断。动态CT显示延迟期低密度肿瘤,提示包膜覆盖病变。EOB-MRI显示T1加权像上肿块呈低信号强度,T2加权像上有高信号强度区域,肝胆期肿块呈低信号,在基于扩散加权成像的表观扩散系数图上呈高信号。FDG-PET显示[F]-FDG无摄取。基于这些影像学检查结果,初步诊断为多发性硬化型肝细胞癌,并行肝尾状叶切除术及S2和S6段部分肝切除术。组织病理学检查显示肿瘤由大小不等的不规则扩张血管组成,伴有一些血栓、炎性细胞浸润、纤维和玻璃样变硬化或黏液瘤样间质,最终诊断为多发性肝硬化性血管瘤。
多发性硬化性血管瘤与其他肝恶性肿瘤,如肝内胆管癌、转移性肝癌以及以丰富纤维间质为特征的硬化型肝细胞癌难以鉴别,因为其影像学表现非常相似。在多发性肝肿瘤的鉴别诊断中考虑肝硬化性血管瘤有助于实现最佳治疗;在计划侵入性治疗前考虑这种可能性很重要。