Clinical characteristics and managements of congenital hepatic hemangioma: a cohort study of 211 cases.

IF 5.9 2区 医学 Q1 GASTROENTEROLOGY & HEPATOLOGY Hepatology International Pub Date : 2024-11-29 DOI:10.1007/s12072-024-10756-5
Xue Gong, Min Yang, Zixin Zhang, Tong Qiu, Jiangyuan Zhou, Wei Shan, Xuepeng Zhang, Yuru Lan, Pingqian Bao, Zilong Zhou, Congxia Yang, Yujia Zhang, Tianliang Li, Jing Guo, Jun Guo, Guoyan Lu, Feiteng Kong, Yongbo Zhang, Siyuan Chen, Yi Ji
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Abstract

Background: Hepatic hemangiomas can be classified into three morphologic patterns: focal (congenital hepatic hemangiomas [CHHs]), multifocal, and diffuse. We aimed to identify the clinical characteristics of CHH and evaluate the changes in CHH management at our institution over the last 2 decades.

Methods: This was a retrospective cohort study of children diagnosed with CHH who were managed at 8 investigation sites. The primary outcome was changes in CHH size in patients at the last follow-up. The primary exposure of interest was management modality in 2 study periods (2003-2012 versus 2013-2022).

Results: Two hundred and eleven patients were analyzed. Four different subtypes of CHH were identified. Rapidly involuting CHH patients had complete involution/nearly complete involution, with a median age of 12.0 months. Noninvoluting CHH presented no change in CHH size. Partially involuting CHH patients presented with partial involution and had a stable tumor size at a median age of 16.0 months. Postnatally proliferating CHHs had an initial postnatal increase in CHH lesion size and underwent involution at a median age of 27.0 months. Further analysis revealed that management strategies for CHHs have shifted over time, with the proportion of patients receiving expectant management increasing from 35.4% before 2013 to 77.7% after 2013 (difference, 42.3%; 95% confidence interval 29.3-53.3%). The survival rate of patients with CHH was high (98.6%).

Conclusions: We documented 4 subtypes of CHHs. We found that expectant management strategies have increasingly replaced invasive interventions in patients with CHH over the past 2 decades.

Research registration unique identifying number (uin): We have already registered at Clinicaltrials.gov. The UIN number is NCT03331744.

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211例先天性肝血管瘤的临床特点及治疗:一项队列研究。
背景:肝血管瘤可分为三种形态:局灶性(先天性肝血管瘤[CHHs])、多灶性和弥漫性。我们的目的是确定CHH的临床特征,并评估过去20年来我院CHH管理的变化。方法:对8个调查地点诊断为CHH的儿童进行回顾性队列研究。主要结果是最后一次随访时患者CHH大小的变化。在2个研究期间(2003-2012年和2013-2022年),主要感兴趣的暴露是管理方式。结果:对211例患者进行了分析。鉴定出四种不同的CHH亚型。迅速复发的CHH患者完全/几乎完全复发,中位年龄为12.0个月。非包络性CHH的大小没有变化。部分复发CHH患者表现为部分复发,肿瘤大小稳定,中位年龄为16.0个月。出生后增殖性CHH的初始出生后CHH病变大小增加,并在27.0个月时复旧。进一步分析显示,CHHs的管理策略随着时间的推移而发生变化,接受预期管理的患者比例从2013年之前的35.4%上升到2013年之后的77.7%(差异为42.3%;95%置信区间29.3-53.3%)。CHH患者生存率高(98.6%)。结论:我们记录了4种CHHs亚型。我们发现,在过去的20年里,对CHH患者,预期治疗策略越来越多地取代了侵入性干预。研究注册唯一识别码:我们已经在Clinicaltrials.gov上注册了。号码为NCT03331744。
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来源期刊
Hepatology International
Hepatology International 医学-胃肠肝病学
CiteScore
10.90
自引率
3.00%
发文量
167
审稿时长
6-12 weeks
期刊介绍: Hepatology International is the official journal of the Asian Pacific Association for the Study of the Liver (APASL). This is a peer-reviewed journal featuring articles written by clinicians, clinical researchers and basic scientists is dedicated to research and patient care issues in hepatology. This journal will focus mainly on new and emerging technologies, cutting-edge science and advances in liver and biliary disorders. Types of articles published: -Original Research Articles related to clinical care and basic research -Review Articles -Consensus guidelines for diagnosis and treatment -Clinical cases, images -Selected Author Summaries -Video Submissions
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