Assessment of focal liver lesions in non-cirrhotic liver – expert opinion statement by the Swiss Association for the Study of the Liver and the Swiss Society of Gastroenterology

Mikael Sawatzki, Daniela B. Husarik, David Semela
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Abstract

Focal liver lesions are common, with a prevalence up to 20%. The lesions must be evaluated in context of risk factors associated with malignancy. Risk factors include age >40 years, known current or past malignancy, presence of liver cirrhosis or chronic liver disease (i.e. suspected by elevated liver elastography measurement ≥8 kPa or FIB-4 score ≥1.3), unintentional weight loss, fever or night sweats, newly detected focal liver lesions, documented growth of focal liver lesions, current or past use of androgens (e.g. testosterone, oxymetholone, danazol), increased serum tumour markers (i.e. alpha-fetoprotein, carbohydrate antigen 19-9 [CA19-9], carcinoembryonic antigen [CEA]) and family history of malignancy. In patients without risk factors of malignancy, regional (non-)fatty changes, simple liver cysts and typical haemangiomas can be diagnosed by conventional ultrasound (without contrast). Conventional ultrasound Doppler is recommended to rule out vascular malformations such as portosystemic shunts. In all other cases of focal liver lesions, contrast-enhanced imaging is indicated for differentiation in benign and malignant dignity. Contrast-enhanced ultrasound (CEUS) as a first diagnostic step and contrast-enhanced magnetic resonance imaging (MRI) are accurate tests to diagnose haemangioma and focal nodular hyperplasia. Hepatocellular adenoma is diagnosed by contrast-enhanced MRI and/or histology. “Wash out” on CEUS is highly suspicious for a malignant focal liver lesion. Additional investigations aimed at identifying the primary tumour, as well as staging-computed tomography, MRI and/or histology may be necessary and should be decided on a case-by-case basis. A biopsy of focal liver lesions is indicated in cases of unclear dignity, malignant aspect and focal liver lesions of unclear origin as well as for guiding surgical and oncological management.
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非肝硬化肝局灶性肝损害的评估-瑞士肝脏研究协会和瑞士胃肠病学会的专家意见声明
局灶性肝脏病变是常见的,患病率高达20%。病变必须在与恶性肿瘤相关的危险因素的背景下进行评估。危险因素包括年龄40岁、已知的当前或过去的恶性肿瘤、存在肝硬化或慢性肝病(即通过肝弹性图测量升高≥8 kPa或FIB-4评分≥1.3怀疑)、意外体重减轻、发烧或夜间出汗、新发现的局灶性肝脏病变、记录的局灶性肝脏病变的生长、目前或过去使用雄性激素(如睾酮、氧美洛酮、那那唑)、血清肿瘤标志物(即甲胎蛋白)升高、糖类抗原19-9 [CA19-9]、癌胚抗原[CEA])与恶性肿瘤家族史的关系。在没有恶性肿瘤危险因素的患者中,局部(非)脂肪改变、单纯性肝囊肿和典型的血管瘤可通过常规超声(不需要对比)诊断。常规超声多普勒建议排除血管畸形,如门静脉分流。在所有其他局灶性肝脏病变病例中,对比增强成像可用于区分良恶性尊严。对比增强超声(CEUS)作为诊断的第一步,对比增强磁共振成像(MRI)是诊断血管瘤和局灶性结节增生的准确测试。肝细胞腺瘤通过增强MRI和/或组织学诊断。超声造影显示“冲洗”是高度可疑的恶性局灶性肝脏病变。其他旨在确定原发肿瘤的调查,以及分期-计算机断层扫描,MRI和/或组织学可能是必要的,应根据具体情况决定。肝局灶性病变活检是指在尊严不明确,恶性方面和起源不明确的情况下,以及指导手术和肿瘤治疗。
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Assessment of focal liver lesions in non-cirrhotic liver – expert opinion statement by the Swiss Association for the Study of the Liver and the Swiss Society of Gastroenterology [Postpartum depression]. [Congenital atransferrinemia]. [Neuroendocrine carcinoma]. [Heart transplantation].
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