首页> 外文期刊>American Journal of Surgical Pathology >Primary hepatic malignant fibrous histiocytoma: clinicopathologic characteristics and prognostic value of ezrin expression.
【24h】

Primary hepatic malignant fibrous histiocytoma: clinicopathologic characteristics and prognostic value of ezrin expression.

机译:原发性肝恶性纤维组织细胞瘤:ezrin表达的临床病理特征和预后价值。

获取原文
获取原文并翻译 | 示例
获取外文期刊封面目录资料

摘要

Primary hepatic malignant fibrous histiocytoma (MFH) is a rare entity with ill-defined clinicopathologic characteristics. We present the largest series to date (7 cases) of primary hepatic MFH, a systematic review of 27 cases published in the English literature, and an analysis of prognostic factors including ezrin expression. The 2 men and 5 women in our series were 34 to 80 years old (average 61 y) and presented with abdominal pain (6/7), systemic symptoms of low-grade fever, malaise, anorexia and weight loss (4/7), and spiking fever (1/7). One case was an incidental finding. Computed tomography and ultrasound revealed a well-demarcated solitary heterogeneous low-density mass ranging from 5.5 to 20 cm (average 12 cm) in largest dimension (5/7), or multiple small nodules up to 2 cm in diameter (1/7) or a 10 cm multiloculated cystic lesion owing to extensive necrosis (1/7). Histologically, a storiform-pleomorphic pattern with variable degrees of necrosis predominated (6/7). A myxoid pattern was seen inonly 1 case and this case lacked necrosis. Lymphoplasmacytic infiltration was seen in 3/7 of the cases. Tumors were grade I (1/7), grade II (2/7), grade III (4/7), stage pT1 (4/7), pT2 (1/7), pT4 (1/7), and pT4, cM1 (1/7) at diagnosis. Three patients with tumor cell ezrin immunoreactivity score >or=1 died of tumor within 1 year. Two patients with tumor cell ezrin immunoreactivity score <1 survived >4 years after surgery. Combined analysis of our series and previously reported cases suggest that primary hepatic MFH possess certain characteristic clinicopathologic features that may help in making the diagnosis and in differentiating it from other more common neoplasms in the liver. The prognosis of hepatic MFH depends primarily on tumor size and stage at the time of diagnosis. Ezrin expression in tumor cells can provide additional prognostic information and may be a potential target for new adjuvant therapies.
机译:原发性肝恶性纤维组织细胞瘤(MFH)是一种罕见的实体,其临床病理特征不明确。我们介绍了迄今为止最大的原发性肝MFH系列病例(7例),对英国文献中发表的27例病例进行了系统综述,并对包括ezrin表达在内的预后因素进行了分析。我们系列中的2名男性和5名女性年龄在34至80岁之间(平均61岁),并表现出腹痛(6/7),低烧,全身乏力,厌食和体重减轻的全身症状(4/7)和尖峰发烧(1/7)。一个案例是一个偶然发现。计算机断层扫描和超声检查显示,界限清晰的孤立异质低密度肿块的最大尺寸(5/7)范围为5.5至20 cm(平均12 cm),或多个直径不超过2 cm的小结节(1/7)或由于广泛的坏死(1/7)而导致的10厘米多位置囊性病变。从组织学上讲,具有可变程度的坏死的星形状多形性模式占主导(6/7)。仅1例可见粘液样,且此例无坏死。在3/7的病例中发现了淋巴浆细胞浸润。肿瘤为I级(1/7),II级(2/7),III级(4/7),pT1期(4/7),pT2(1/7),pT4(1/7)和pT4 ,诊断时为cM1(1/7)。 3名肿瘤细胞ezrin免疫反应性评分≥1的患者在1年内死于肿瘤。肿瘤细胞ezrin免疫反应评分<1的两名患者在手术后存活> 4年。对我们的系列病例和先前报道的病例的综合分析表明,原发性肝MFH具有某些特征性的临床病理特征,可能有助于做出诊断并将其与肝脏中其他较常见的肿瘤区分开。肝MFH的预后主要取决于诊断时的肿瘤大小和分期。肿瘤细胞中Ezrin的表达可提供其他预后信息,并且可能是新辅助疗法的潜在靶标。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号