Department of Radiodiagnosis, All India Institute of Medical Sciences (A.I.I.M.S), New Delhi, India.
Department of Radiodiagnosis, All India Institute of Medical Sciences (A.I.I.M.S), New Delhi, India.
Curr Probl Diagn Radiol. 2022 Jan-Feb;51(1):73-85. doi: 10.1067/j.cpradiol.2020.10.001. Epub 2020 Nov 2.
The radiological appearance of common primary hepatic tumors such as hepatocellular carcinoma (HCC) and cholangiocarcinoma (CCA) is widely recognized. Hepatic masses with unusual histology are occasionally encountered, but seldom suspected on imaging. However, many possess characteristic imaging findings, which when assessed along with the clinical and demographic background and serum tumor markers, may enable a prospective diagnosis. This review attempts to familiarize the reader with the clinicopathological characteristics, imaging manifestations, and differential diagnosis of these unusual liver tumors in adults. Biphenotypic primary liver carcinoma is suspected in masses showing distinct areas of HCC and CCA-type enhancement pattern in cirrhotic livers. Fibrolamellar carcinoma occurs in young individuals without underlying chronic liver disease and shows a characteristic T2-hypointense scar frequently showing calcification. Perivascular epithelioid cell tumors are differentials for any arterial hyperenhancing mass in the noncirrhotic liver, particularly in patients with tuberous sclerosis. Multifocal subcapsular tumors showing target-like morphology, capsular retraction and "lollipop" sign are suspicious for epithelioid hemangioendothelioma. On the other hand, multiple hemorrhagic lesions showing patchy areas of bizarre-shaped arterial phase hyperenhancement are suspicious for angiosarcoma. Primary hepatic lymphoma (PHL) is suspected when patients with immunosuppression present with solitary or multifocal masses that insinuate around vessels and bile ducts without causing luminal narrowing. Intense diffusion restriction and low-level homogeneous or target-like enhancement are also ancillary features of PHL. Primary hepatic neuroendocrine tumor shows uptake on Ga-68 DOTANOC PET/CT. Although a straightforward diagnosis may be difficult in these cases, awareness of the characteristic imaging appearances is helpful in suspecting the diagnosis.
常见原发性肝肿瘤(如肝细胞癌 [HCC] 和胆管细胞癌 [CCA])的放射学表现广为人知。虽然偶尔会遇到具有不寻常组织学的肝肿块,但在影像学上很少被怀疑。然而,许多具有特征性的影像学表现,如果结合临床和人口统计学背景以及血清肿瘤标志物进行评估,可能能够做出前瞻性诊断。本综述旨在使读者熟悉这些成人不常见肝肿瘤的临床病理特征、影像学表现和鉴别诊断。在肝硬化肝脏中,具有 HCC 和 CCA 型增强模式的明显区域的肿块,提示存在双表型肝癌。纤维板层样肝细胞癌发生在无潜在慢性肝病的年轻个体中,表现为特征性 T2 低信号瘢痕,常伴有钙化。血管周上皮样细胞瘤是任何非肝硬化肝脏中动脉高增强肿块的鉴别诊断,特别是在结节性硬化症患者中。表现为靶样形态、包膜回缩和“棒棒糖”征的多灶性包膜下肿瘤,提示上皮样血管内皮细胞瘤。另一方面,表现为多灶性出血性病变、斑片状奇异型动脉期高增强的病变,提示为血管肉瘤。当免疫抑制患者出现单发或多发病灶,围绕血管和胆管生长而不引起管腔狭窄时,应怀疑原发性肝淋巴瘤(PHL)。弥散受限明显、低水平均匀或靶样增强也是 PHL 的辅助特征。原发性肝神经内分泌肿瘤在 Ga-68 DOTANOC PET/CT 上摄取。尽管这些情况下可能难以做出直接诊断,但了解特征性影像学表现有助于怀疑诊断。