Division of Gastroenterology and Hepatology, Department of Medicine, Indiana University School of Medicine, Indianapolis, Indiana, USA.
Division of Gastroenterology and Hepatology, Department of Medicine, University of Pennsylvania School of Medicine, Philadelphia, Pennsylvania, USA.
Am J Gastroenterol. 2022 Jul 1;117(7):1089-1096. doi: 10.14309/ajg.0000000000001743. Epub 2022 Mar 23.
Beyond oral contraceptives (OCs), metabolic factors have been suggested to increase the risk of hepatocellular adenoma (HCA). The impact of risks remains poorly defined, particularly among men and those with adenomatosis. Thus, we aimed to examine HCA clinical and outcome characteristics through a large multicenter cohort.
HCA diagnosis was made based on a combination of clinical, radiologic, and histologic criteria. Patient and clinical data including follow-up imaging, complications, and interventions were collected between 2004 and 2018 from 3 large academic centers.
Among 187 patients (163 female and 24 male) with HCA, 75 had solitary HCA, 58 had multiple HCAs, and 54 had adenomatosis. Over a median follow-up of 3.3 years (quartile 1: 1.2, quartile 3: 8.8), 34 patients (18%) had radiologic interventions, 41 (21%) had surgical resections, 10 (5%) developed tumoral hemorrhage, and 1 had malignant transformation. OC and corticosteroid use were present in 70% and 16%, respectively. Obesity (51%), type 2 diabetes (24%), hypertension (42%), and hypertriglyceridemia (21%) were also common. Metabolic comorbidities were more common in patients with large HCAs and adenomatosis. Compared with women, men had less hepatic steatosis (4% vs 27%), smaller HCAs (2.3 cm vs 4.4 cm), and more corticosteroid use (38% vs 11%) ( P < 0.05 for all). With OC cessation, 69% had a decrease in size of HCA, but 25% eventually required advanced interventions.
In this large HCA cohort, obesity and metabolic comorbidities were important risk factors associated with large HCAs and adenomatosis. Long-term adverse outcomes were infrequent, 5% had tumor hemorrhage, and 1 patient exhibited malignant transformation.
除了口服避孕药(OC),代谢因素也被认为会增加肝细胞腺瘤(HCA)的风险。这些风险的影响仍未得到明确界定,尤其是在男性和腺瘤病患者中。因此,我们旨在通过一个大型多中心队列来研究 HCA 的临床和结局特征。
HCA 的诊断基于临床、影像学和组织学标准的综合判断。我们于 2004 年至 2018 年期间,从 3 个大型学术中心收集了患者和临床数据,包括随访影像学、并发症和干预措施。
在 187 例 HCA 患者(163 名女性和 24 名男性)中,75 例为单发 HCA,58 例为多发 HCA,54 例为腺瘤病。在中位数为 3.3 年(四分位距 1:1.2,3:8.8)的随访中,34 例(18%)患者接受了影像学干预,41 例(21%)接受了手术切除,10 例(5%)发生了肿瘤出血,1 例发生了恶性转化。OC 和皮质类固醇的使用率分别为 70%和 16%。肥胖(51%)、2 型糖尿病(24%)、高血压(42%)和高三酰甘油血症(21%)也很常见。大的 HCA 和腺瘤病患者中更常见代谢合并症。与女性相比,男性的肝脂肪变性(4%比 27%)更少,HCA 更小(2.3cm 比 4.4cm),皮质类固醇使用率更高(38%比 11%)(所有 P 值均<0.05)。OC 停药后,69%的 HCA 大小减小,但 25%最终需要进行高级干预。
在这个大型 HCA 队列中,肥胖和代谢合并症是与大的 HCA 和腺瘤病相关的重要危险因素。长期不良结局很少见,有 5%的患者发生肿瘤出血,1 例发生恶性转化。