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原发性肝脏肉瘤2例报告并文献综述 被引量:2

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摘要 目的探讨原发性肝脏肉瘤的临床和影像学相对的规律,提高对肝脏肉瘤的认识。方法回顾性分析2例经病理证实的肝脏肉瘤(肝成骨肉瘤、肝血管肉瘤各1例)的临床资料和影像学资料,结合文献进行分析、总结原发性肝脏肉瘤、肝成骨肉瘤及肝血管肉瘤的临床和影像学表现。结果原发性肝脏肉瘤发病率低,男性、中老年人相对多见,无特异性临床症状和体征,肿瘤标志物常在正常范围,常无肝炎、肝硬化背景。肝脏成骨肉瘤多表现为上腹部或肝脏巨大肿块,边界不清,内可见不规则钙化;肝血管肉瘤常呈多发结节,可以伴出血、坏死、囊性变、纤维化或钙化,增强扫描造影剂呈渐进性向心性填充,与血管瘤相似,但较血管瘤更易出血、坏死。肝脏肉瘤预后均很差,5年生存率约14%,积极手术切除病灶及辅助化疗是提高生存率的有效方法。结论肝脏肉瘤临床较少见,因其恶性度高、预后差,提高对肝脏肉瘤的临床和影像学特点的认识,有助于早期诊断、正确诊断,对延长患者生存期至关重要。
出处 《罕少疾病杂志》 2013年第1期7-12,共6页 Journal of Rare and Uncommon Diseases
基金 国家科技支撑计划项目(编号:2013BAI07B100)
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