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Computed tomography imaging and clinical features of congenital hepatoblastoma: A retrospective analysis

机译:先天性肝细胞瘤的计算机断层摄影成像和临床特征:回顾性分析

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Congenital hepatoblastoma (CHB) is the most common hepatic malignant tumor of fetus or neonates , but few studies focusing on the radiological characteristics of CHB have been reported to date. To investigate the characteristic clinical and computed tomography (CT) findings of CHB to facilitate recognition and noninvasive diagnosis. Medical records of 7 patients with CHB were retrospectively reviewed. The demographic, clinical, and laboratory data were extracted from the electronic medical records. Two pediatric radiologists evaluated the abdominal CT examinations for the hepatic tumor location, size, enhancement characteristics, vascular invasion, and intra-/extra-hepatic metastasis. Among the included 7 patients (3 males and 4 females), only 1 had an elevated serum alpha-fetoprotein level. All patients had solitary intrahepatic mass with a mean size of 4.7 cm (range: 2.9–10.2 cm), of which liver SV-VII were most involved. 4/7 tumors were round while 3/7 irregular or lobulated. 6/7 tumors were well-defined. Microhemorrhage, cystic necrosis, and coarse calcification were present in 5/7, 4/7, and 1/7 tumors, respectively. All lesions showed inhomogeneously significant enhancement, with multiple nodular or striped appearance in the center and periphery of the tumors on the arterial phase, and then the enhancement area showed progressive expansion and fusion filling over time but the attenuation gradually declined on the portal and delayed phases, and finally the majority (6/7) of tumors presented multiple band- or island-like characteristics with prominently peripheral enhancement on the delayed phase while the remaining 1 relatively small tumor showed nearly complete but inhomogenous enhancement. In addition, only 1/7 tumor had hilar hepatic bile duct and portal vein invasion and secondary intra-hepatic bile duct dilation. No metastatic lesions were identified in all patients at diagnosis. The abdominal aorta distal to the coeliac trunk was significantly narrowed in 3/7 patients. Pathological examinations suggested that 6/7 tumors showed fetal histology with only 1 containing mesenchymal elements. The relationship between serum alpha-fetoprotein and CHB could be more complicated and yet to be determined. Dynamic contrast-enhanced CT can facilitate recognition and noninvasive diagnosis of CHB, presenting a pattern of progressive expansion and fusion filling but inhomogeneously significant enhancement.
机译:先天性肝细胞瘤(CHB)是胎儿或新生儿最常见的肝脏恶性肿瘤,但迄今已举报少数关注CHB的放射性特征的研究。探讨CHB的特征临床和计算断层扫描(CT)结果,以促进识别和非侵入性诊断。回顾性审查了7例CHB患者的病历。从电子医疗记录中提取了人口统计学,临床和实验室数据。两位儿科放射学家评估了肝肿瘤位置,大小,增强特征,血管侵袭和肝癌中的腹部CT检查。在包含的7名患者中(3名男性和4名女性)中,只有1只具有升高的血清α-胎蛋白水平。所有患者均具有4.7厘米(范围:2.9-10.2厘米)的平均肝内质量,其中肝脏SV-VII最涉及。 4/7肿瘤是圆形的,而3/7不规则或裂解。定义了6/7肿瘤。在5/7,4 / 7和1/7肿瘤中分别存在微血清,囊性坏死和粗钙化。所有病变表现出在动脉阶段的肿瘤的中心和周边中具有多个结节或条纹外观,然后随着时间的推移,增强区域显示逐渐膨胀和融合,但衰减逐渐下降在门户网上和延迟阶段最后,大多数(6/7)的肿瘤呈现多个带状或岛状特征,延迟阶段突出的外周提高,而剩余的1个相对小的肿瘤显示几乎完全但均匀的增强。此外,只有1/7肿瘤患有肺肝胆管和门静脉侵袭和二次内肝胆管扩张。在诊断的所有患者中没有鉴定转移性病变。对腹腔躯干远离腹部主动脉在3/7患者中显着缩小。病理检查表明,6/7肿瘤显示胎儿组织学,仅具有1个间充质元素。血清α-胎蛋白和CHB之间的关系可以更复杂并且尚未确定。动态对比度增强CT可以促进CHB的识别和非侵入性诊断,呈现逐渐膨胀和融合填充的模式,但不均匀地显着提高。

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