[Primary hepatic sarcomatoid carcinoma, an unusual case].

IF 0.6 4区 医学 Q3 MEDICINE, GENERAL & INTERNAL
Medicina-buenos Aires Pub Date : 2024-01-01
Darío A Rueda, Florencia Antinucci, Marcelo F Amante, Carlos A Bas
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引用次数: 0

Abstract

Primary hepatic sarcomatoid carcinoma is a very aggressive tumor, representing 0.4-0.7% of all primary hepatic neoplasms. The disease is associated with liver disease due to hepatotropic viruses and is more prevalent in Asians. Histology shows sarcomatous and carcinoma components. It does not have pathognomonic clinical or imaging characteristics and its diagnosis is based on the pathological and immunohistochemistry findings. Surgery could prolong survival in localized stages. We report the case of a 72-year-old Korean patient with a history of chronic liver disease due to B virus, who was diagnosed with primary hepatic sarcomatoid carcinoma with bone and lymph node metastases.

[原发性肝肉瘤样癌,一个不寻常的病例]。
原发性肝肉瘤样癌是一种侵袭性很强的肿瘤,占所有原发性肝肿瘤的0.4%-0.7%。这种疾病与致肝病毒引起的肝病有关,在亚洲人中发病率较高。组织学显示有肉瘤和癌成分。它没有临床或影像学特征,诊断依据是病理和免疫组化结果。手术可延长局部分期患者的生存期。我们报告了一例 72 岁韩国患者的病例,该患者曾因 B 病毒导致慢性肝病,被诊断为原发性肝肉瘤样癌,并伴有骨和淋巴结转移。
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
Medicina-buenos Aires
Medicina-buenos Aires 医学-医学:内科
CiteScore
1.30
自引率
12.50%
发文量
0
审稿时长
6-12 weeks
期刊介绍: Information not localized
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