在囊性纤维化中肝细胞癌 肝脏疾病 肝脏疾病
Rama Tarakji1, Sunny Sandhu2, Eric F Martin2
1Department of Medicine, Mt. Sinai Medical Center, Miami, Florida.
Gastro hep advances
|September 8, 2025
概括
囊性纤维化肝病 (CFLD) 在成年人中越来越常见. 本案例研究突出了一个罕见的肝细胞癌在一个成年人的CFLD,成功地通过微波切除治疗的例子.
科学领域:
- 肝病学 肝病学是一种肝病学.
- 胃肠病学 胃肠病学
- 在瘤学瘤学.
背景情况:
- 囊性纤维化 (CF) 的生存率有所改善,导致成人病例增加.
- 囊性纤维化肝病 (CFLD) 在成年人中越来越令人担忧,成为第三大死亡原因.
- 肝细胞癌 (HCC) 是一种极为罕见的CFLD并发症.
研究的目的:
- 报告一种异常罕见的肝细胞癌 (HCC) 病例,该病例发生在患有囊性纤维化肝病 (CFLD) 的成年人身上.
- 描述使用微波切除的CFLD相关HCC的成功治疗方法.
主要方法:
- 案例报告的呈现方式.
- 对患有CFLD和HCC的患者的临床数据的审查.
- 描述微波除作为一种治疗方式.
主要成果:
- 一名患有CFLD的患者患有肝细胞癌 (HCC),这是一个非常罕见的现象.
- 患者的HCC被有效地使用微波切除治疗.
- 在不断增长的成年CF群体中成功管理一种罕见的并发症.
结论:
- 肝细胞癌 (HCC) 可能发生在患有囊性纤维化肝病 (CFLD) 的成年人中,尽管很少见.
- 微波除是一种可行且成功的治疗选择,用于CFLD相关的HCC.
- 在老化中的CFLD人口中,可能需要加强对HCC的监测.
更多相关视频
12:24A Three-Dimensional Spheroid Model to Investigate the Tumor-Stromal Interaction in Hepatocellular Carcinoma
Published on: September 30, 2021
6.0K
06:38An Oncogenic Hepatocyte-Induced Orthotopic Mouse Model of Hepatocellular Cancer Arising in the Setting of Hepatic Inflammation and Fibrosis
Published on: September 12, 2019
9.4K
相关概念视频
Cystic Fibrosis: Pathogenesis
730
Cystic fibrosis (CF), an autosomal recessive disorder, significantly affects the function of exocrine glands. This genetically inherited disease is characterized by the production of thick and sticky mucus, which can severely affect various organs and systems in the body.
CF is primarily caused by a genetic mutation in a chromosome 7 gene coding for the cystic fibrosis transmembrane conductance regulator (CFTR) protein. The most common gene mutation leading to CF is the ΔF508 mutation,...
CF is primarily caused by a genetic mutation in a chromosome 7 gene coding for the cystic fibrosis transmembrane conductance regulator (CFTR) protein. The most common gene mutation leading to CF is the ΔF508 mutation,...
730
Cystic Fibrosis: Management
477
Cystic fibrosis (CF) is an autosomal recessive disorder that predominantly affects individuals of Northern European descent, occurring at a rate of 1 in 3500. It is caused by a genetic mutation in a gene on chromosome 7, most commonly the ΔF508 mutation, that codes for the cystic fibrosis transmembrane conductance regulator (CFTR) protein. This results in thicker mucus secretions and obstruction pathologies in multiple organs, including the lungs and sinuses.
Sinus disease and chronic...
Sinus disease and chronic...
477
