Targeted-gene sequencing of an undifferentiated gallbladder carcinoma: a case report

被引:3
作者
Xiao, Ying [1 ]
Xiang, Canhong [2 ]
Yang, Di [1 ]
Zhao, Benqi [3 ]
Li, Yong [1 ]
Yin, Hongfang [1 ]
机构
[1] Tsinghua Univ, Beijing Tsinghua Changgung Hosp, Sch Clin Med, Dept Pathol, Beijing, PR, Peoples R China
[2] Tsinghua Univ, Beijing Tsinghua Changgung Hosp, Sch Clin Med, Dept Hepatopancreatobiliary Surg, Beijing, Peoples R China
[3] Tsinghua Univ, Beijing Tsinghua Changgung Hosp, Sch Clin Med, Dept Radiol, Beijing, Peoples R China
关键词
Undifferentiated carcinoma; Gallbladder carcinoma; Case report; Targeted gene sequencing; Tumor mutation burden; INTRATUMOR HETEROGENEITY; SPINDLE; TUMOR;
D O I
10.1186/s13000-020-00981-5
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
Background Undifferentiated carcinomas of the gallbladder are extremely rare. Most undifferentiated carcinomas are accompanied by adjacent foci of other conventional carcinomas, and a transition zone is shared between them. However, genetic alterations of undifferentiated gallbladder carcinoma and the similarities or differences between the undifferentiated carcinoma and the foci conventional carcinoma are unknown. Case presentation Herein, we report a case of undifferentiated gallbladder carcinoma with osteoclast-like giant cells with invasion into the liver, duodenum, and stomach in a 56-year-old man. The tumor was microscopically formed from the tubular adenocarcinoma (< 5% of the entire tumor), the undifferentiated carcinoma, and a transition zone between them. Four somatic mutations (TP53, TERT, ARID2, and CDH1), three amplifications (CCND1, FGF19, and MET), and a tumor mutation burden (TMB) of 3.45 muts/Mb were detected in the undifferentiated component using targeted gene sequencing, whereas 102 somatic mutations (including TP53, TERT, ARID2, and CDH1), one amplification (CCND1), and a higher TMB of 87.07 muts/Mb were detected in the tubular component. This patient died of tumor recurrence 2 months after the surgery. Conclusions The undifferentiated gallbladder carcinoma had its unique molecular alterations. The similarities in the genetic alterations of the undifferentiated carcinoma and adenocarcinoma provide evidence of a common origin at the genetic level. The occurrence of an undifferentiated carcinoma may be due to heterogeneity-associated branched evolution from the tubular adenocarcinoma.
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