"Update on pediatric primary liver tumors".

IF 3.4 3区 医学 Q1 PATHOLOGY Virchows Archiv Pub Date : 2025-01-01 Epub Date: 2025-01-21 DOI:10.1007/s00428-024-03985-4
Dolores López-Terrada, Jens Stahlschmidt, Antonio R Pérez-Atayde
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Abstract

Liver masses are common in children, however primary malignant neoplasms are rare, representing only 1% of all pediatric cancers. Hepatocellular neoplasms are the most common primary liver malignancies and hepatoblastoma (HB) is the most frequently diagnosed. The incidence of HB, which is increasing, is approximately of 2 cases per million in the United States, followed by hepatocellular carcinoma (HCC). Pediatric primary liver tumors of mesenchymal origin are less common, except for benign vascular tumors (hemangiomas). Malignant mesenchymal neoplasms represent approximately 10-15% of all, the most common being embryonal sarcoma and malignant rhabdoid tumor. Malignant vascular tumors are rare, but epithelioid hemangioendothelioma (EHE) and angiosarcoma can be seen in children. The development and adoption of consensus diagnostic, therapeutic and risk-stratifying approaches for pediatric patients with malignant liver tumors has been historically challenged by their rarity and by their diverse clinical and histological appearance. On-going collaborative efforts of international consortia including the Children's Oncology Group (COG) in North America, the German Society of Paediatric Oncology and Haematology (GPOH), the Societe Internationale d' Oncologie Pediatrique Liver Tumor Study Group (SIOPEL) in Europe and the Japanese Liver Tumor group (JPLT), have made significant contributions to understanding the clinical and histopathological features, as well as the underlying biology of pediatric liver tumors, in particular HB. A new classification of pediatric liver tumors drafted at the international consensus meeting held in Los Angeles, has been incorporated in the recent WHO classification and is currently used by the PHITT (Paediatric Hepatic Malignancy International Tumour Trial) and other therapeutic protocols. This manuscript provides an overview of salient diagnostic features and updates in classification and molecular characterization for the most common pediatric primary liver neoplasms. It also includes a brief overview of other less common but relevant tumors, which should be considered in the differential diagnosis.

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《儿童原发性肝脏肿瘤最新进展》。
肝脏肿块在儿童中很常见,然而原发性恶性肿瘤是罕见的,仅占所有儿童癌症的1%。肝细胞肿瘤是最常见的原发性肝脏恶性肿瘤,肝母细胞瘤(HB)是最常见的诊断。HB的发病率正在增加,在美国大约为每百万人中有2例,其次是肝细胞癌(HCC)。除了良性血管瘤(血管瘤)外,小儿原发性肝间质肿瘤较少见。恶性间充质肿瘤约占所有肿瘤的10-15%,最常见的是胚胎肉瘤和恶性横纹肌样瘤。恶性血管肿瘤是罕见的,但上皮样血管内皮瘤(EHE)和血管肉瘤可以在儿童中看到。由于小儿恶性肝肿瘤的罕见性及其临床和组织学表现的多样性,发展和采用一致的诊断、治疗和风险分层方法一直受到历史上的挑战。包括北美儿童肿瘤小组(COG)、德国儿科肿瘤和血液学学会(GPOH)、欧洲国际肿瘤学会儿童肝脏肿瘤研究组(SIOPEL)和日本肝脏肿瘤小组(JPLT)在内的国际联盟正在进行的合作努力,为了解儿童肝脏肿瘤的临床和组织病理学特征以及潜在生物学做出了重大贡献。特别是HB。在洛杉矶举行的国际共识会议上起草的儿科肝脏肿瘤新分类已被纳入世卫组织最近的分类,目前被PHITT(儿科肝脏恶性肿瘤国际肿瘤试验)和其他治疗方案所使用。这份手稿提供了一个突出的诊断特征和更新的分类和分子表征最常见的儿科原发性肝脏肿瘤的概述。它还包括对其他不常见但相关的肿瘤的简要概述,这些肿瘤应在鉴别诊断中加以考虑。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Virchows Archiv
Virchows Archiv 医学-病理学
CiteScore
7.40
自引率
2.90%
发文量
204
审稿时长
4-8 weeks
期刊介绍: Manuscripts of original studies reinforcing the evidence base of modern diagnostic pathology, using immunocytochemical, molecular and ultrastructural techniques, will be welcomed. In addition, papers on critical evaluation of diagnostic criteria but also broadsheets and guidelines with a solid evidence base will be considered. Consideration will also be given to reports of work in other fields relevant to the understanding of human pathology as well as manuscripts on the application of new methods and techniques in pathology. Submission of purely experimental articles is discouraged but manuscripts on experimental work applicable to diagnostic pathology are welcomed. Biomarker studies are welcomed but need to abide by strict rules (e.g. REMARK) of adequate sample size and relevant marker choice. Single marker studies on limited patient series without validated application will as a rule not be considered. Case reports will only be considered when they provide substantial new information with an impact on understanding disease or diagnostic practice.
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