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原发性肝鳞状细胞癌:病例报告及文献系统综述

Primary hepatic squamous cell carcinoma: case report and systematic review of the literature.

作者信息

Zhao Lin, Zhou Yan, Ding Jianmin, Qin Zhengyi, Zhou Hongyu, Jing Xiang

机构信息

Department of Ultrasound, The Third Central Hospital of Tianjin, Tianjin, China.

Tianjin Key Laboratory of Extracorporeal Life Support for Critical Diseases, Tianjin Third Central Hospital, Tianjin, China.

出版信息

Front Oncol. 2023 Oct 10;13:1229936. doi: 10.3389/fonc.2023.1229936. eCollection 2023.

Abstract

Primary hepatic squamous cell carcinoma (SCC) is extremely rare, and only a few dozen cases have been reported to date. It can barely be diagnosed before histopathological examination, which necessitates the exclusion of metastatic tumors. In this case, we present a 60-year-old female patient with no comorbidity. As laboratory tests and imaging examinations were not diagnostic, ultrasonography (US)-guided liver biopsy was performed and eventually revealed a definitive pathological diagnosis of hepatic SCC. After excluding metastasis, the diagnosis of primary hepatic SCC was established, and then chemotherapy and immunotherapy were performed. Additionally, a comprehensive literature search was conducted on primary hepatic SCC using PubMed, Google Scholar, and Web of Science, and a total of 53 articles were retrieved with a time range from 1972 to 2022. A critical analysis was then performed to evaluate previous literature focusing on the clinical characteristics, imaging features, treatments, and prognosis.

摘要

原发性肝鳞状细胞癌(SCC)极为罕见,迄今为止仅报道了几十例。在组织病理学检查之前几乎无法诊断,这就需要排除转移性肿瘤。在此病例中,我们介绍了一位60岁无合并症的女性患者。由于实验室检查和影像学检查均无法确诊,遂进行了超声(US)引导下的肝活检,最终明确了肝SCC的病理诊断。排除转移后,确立了原发性肝SCC的诊断,随后进行了化疗和免疫治疗。此外,使用PubMed、谷歌学术和科学网对原发性肝SCC进行了全面的文献检索,共检索到53篇文章,时间范围为1972年至2022年。然后进行了批判性分析,以评估以往关于临床特征、影像学特征、治疗方法和预后的文献。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2ab9/10795173/a133e6c1aa8d/fonc-13-1229936-g001.jpg

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