Two Cases of Hepatoblastoma in Adults.

IF 1.9 Q3 PATHOLOGY Clinical Pathology Pub Date : 2022-10-26 eCollection Date: 2022-01-01 DOI:10.1177/2632010X221129592
Elouarith Ihssan, Elagouri Hajar, Bekarsabein Salma, Ech-Charif Soumaya, Mahdi Youssef, Khmou Mouna, El Khannoussi Basma
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引用次数: 1

Abstract

Adult hepatoblastoma is a rare tumor whose etiology and mechanisms of development are still incompletely understood. Imaging and biological tests such as AFP and liver enzymes are non-specific. Histologically, there are 2 histological variants: pure epithelial with 5 types (pure fetal, embryonal, small cell undifferentiated, cholangioblastic, and macrotrabecular), a mixed epithelial and a mesenchymal variant with or without a teratoid contingent. The main differential diagnosis concerns hepatocellular carcinoma. The treatment of hepatoblastoma in adults is not yet standardized and surgery remains the mainstay of treatment. In this report we aim to describe the clinical, pathological, and immunohistochemical features of this rare entity in adult patients and discuss the elements allowing its distinction from hepatocellular carcinoma (HCC).

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成人肝母细胞瘤2例。
成人肝母细胞瘤是一种罕见的肿瘤,其病因和发展机制仍不完全清楚。影像学和生物学检查如甲胎蛋白和肝酶无特异性。组织学上,有2种组织学变异:纯上皮细胞有5种类型(纯胎儿型、胚胎型、未分化小细胞型、成胆管型和大小梁型),混合上皮细胞和间充质变异,伴或不伴畸胎瘤。主要的鉴别诊断涉及肝细胞癌。成人肝母细胞瘤的治疗尚未标准化,手术仍然是主要的治疗方法。在本报告中,我们旨在描述成人患者中这种罕见实体的临床,病理和免疫组织化学特征,并讨论使其与肝细胞癌(HCC)区分的因素。
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来源期刊
Clinical Pathology
Clinical Pathology PATHOLOGY-
CiteScore
2.20
自引率
7.70%
发文量
66
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