Department of Radiology, Nationwide Children's Hospital, ED Bldg, 4th Fl, 700 Childrens Dr, Columbus, OH 43205.
Department of Radiology, University of Texas Southwestern Medical Center, Dallas, TX.
AJR Am J Roentgenol. 2022 Oct;219(4):647-654. doi: 10.2214/AJR.22.27600. Epub 2022 May 11.
Pediatric hepatocellular carcinoma (HCC) is an aggressive malignancy for which imaging findings remain poorly described. In comparison with adult HCC, pediatric HCC more commonly occurs without underlying risk factors, and standardized surveillance guidelines for those with predispositions are lacking. The purpose of this article was to evaluate imaging findings of nonfibrolamellar pediatric HCC and to identify associations between these imaging findings and the presence of predisposing factors. This retrospective study included children (≤ 18 years) with histologically confirmed nonfibrolamellar HCC who underwent multiphase CT or MRI at one of four academic children's hospitals between July 2009 and April 2019. Surveillance regimens in children with predispositions were at the discretion of treating physicians. Clinical characteristics were recorded. Scan indications were classified as surveillance versus clinical signs and symptoms. Images from all sites were submitted to a cloud-based server. Two radiologists independently assessed imaging features of HCC, including tumor size, tumor in vein, Pre-Treatment Extent of Tumor (PRETEXT) stage, and LI-RADS major features of adult HCC. Imaging findings were compared between patients with and without predispositions. The study included 39 patients: 17 with predispositions (mean age, 10.5 ± 4.5 years; nine boys, eight girls) and 22 without predispositions (mean age, 11.3 ± 5.1 years; 12 boys, 10 girls). Scan indication was surveillance in 14/17 patients with predispositions versus 0/22 patients without predispositions ( < .001). Patients with versus those without predispositions had smaller tumor size (reader 1: 6.0 vs 11.9 cm [ = .003]; reader 2: 6.0 vs 12.9 cm [ < .001]) and less frequent tumor in vein (reader 1: 0% vs 41% [ = .002]; reader 2: 0% vs 36% [ = .006]). PRETEXT stage IV disease was observed in 18% (both readers) of patients with predispositions versus 50-55% of patients without predispositions. No LI-RADS major feature of adult HCC showed a significant difference in frequency between patients with and without predispositions for either reader (all > .05). Among children with HCC, those with predispositions exhibited smaller and lower-stage tumors and less frequent tumor in vein, likely because of surveillance imaging. The study supports the role of routine surveillance imaging in children with HCC predispositions to facilitate earlier detection. Standardization of surveillance guidelines remains needed.
儿童肝细胞癌(HCC)是一种侵袭性恶性肿瘤,其影像学表现仍描述不佳。与成人 HCC 相比,儿童 HCC 更常发生于无潜在危险因素的情况下,且缺乏针对具有易患因素的患者的标准化监测指南。本文的目的是评估非纤维板层型儿童 HCC 的影像学表现,并确定这些影像学表现与易患因素之间的关系。本回顾性研究纳入了 2009 年 7 月至 2019 年 4 月在四家学术儿童医院接受多期 CT 或 MRI 检查并经组织学证实为非纤维板层型 HCC 的儿童(≤18 岁)。具有易患因素的儿童的监测方案由治疗医生决定。记录临床特征。扫描指征分为监测与临床症状和体征。所有部位的图像均提交至基于云的服务器。两位放射科医生独立评估 HCC 的影像学特征,包括肿瘤大小、肿瘤静脉内侵犯、治疗前肿瘤范围(PRETEXT)分期和成人 HCC 的 LI-RADS 主要特征。比较了有和无易患因素的患者之间的影像学表现。该研究纳入了 39 例患者:17 例有易患因素(平均年龄 10.5 ± 4.5 岁;9 名男孩,8 名女孩),22 例无易患因素(平均年龄 11.3 ± 5.1 岁;12 名男孩,10 名女孩)。在有易患因素的 17 例患者中,监测为扫描指征的占 14/17,而无易患因素的 22 例患者中扫描指征为监测的占 0/22(<.001)。与无易患因素的患者相比,有易患因素的患者肿瘤更小(reader 1:6.0 比 11.9cm[<.001];reader 2:6.0 比 12.9cm[<.001]),且静脉内侵犯更少见(reader 1:0%比 41%[<.001];reader 2:0%比 36%[<.006])。有易患因素的患者中,有 18%(两位读者)为 PRETEXT 分期 IV 期疾病,而无易患因素的患者中为 50%-55%。对于两位读者,成人 HCC 的 LI-RADS 主要特征在频率上均无显著差异(均>.05)。在 HCC 患儿中,有易患因素的患者肿瘤更小、分期更低,且静脉内侵犯更少见,这可能与监测影像学有关。该研究支持对有 HCC 易患因素的儿童进行常规监测影像学检查,以促进早期发现。仍需要对监测指南进行标准化。