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胰腺伴破骨样巨细胞的未分化癌,携带 KRAS 和 BRCA 突变:病例报告和全外显子组测序分析。

Undifferentiated carcinoma with osteoclast-like giant cells of the pancreas harboring KRAS and BRCA mutations: case report and whole exome sequencing analysis.

机构信息

Department of Medical Oncology, National Cancer Center/National Clinical Research Center for Cancer/ Cancer Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, 100021, China.

Department of Oncology, Shouguang Hospital of Traditional Chinese Medicine, Weifang, 262700, China.

出版信息

BMC Gastroenterol. 2020 Jun 26;20(1):202. doi: 10.1186/s12876-020-01351-7.

Abstract

BACKGROUND

Undifferentiated carcinoma with osteoclast-like giant cells (UC-OGC) is an extremely uncommon pancreatic neoplasm that comprises less than 1% of all exocrine pancreatic tumors. To date, cases and data from whole-exome sequencing (WES) analysis have been reported by specific studies. We report a case of pancreatic UC-OGC with a literature review, and provide novel insights into the molecular characteristics of this tumor entity.

CASE PRESENTATION

A 31-year-old male presented with intermittent abdominal pain for several months, and positron emission tomography (PET) showed isolated high metabolic nodules during the pancreatic uncinate process that were likely to be malignant disease. Pathological examination after radical excision revealed UC-OGC associated with poorly differentiated adenocarcinoma at the head of the pancreas. The disease recurred 7.4 months after radical surgery. The KRAS p.G12D (c.35G > A) and somatic BRCA2 p.R2896C (c.8686C > T) mutations were detected by subsequent WES analysis. The patient showed no response to platinum-based systemic chemotherapy, and his condition quickly worsened. He finally died, with an overall survival of 1 year.

CONCLUSIONS

As an extremely uncommon tumor entity, UC-OGC is really a unique variant of conventional pancreatic ductal adenocarcinoma due to its similarities, as shown by genomic WES analysis. Clinical examination and molecular analysis by WES could further indicate potential treatment strategies for UC-OGC.

摘要

背景

破骨细胞样巨细胞未分化癌(UC-OGC)是一种极罕见的胰腺肿瘤,占所有外分泌胰腺肿瘤的比例不足 1%。迄今为止,已有特定研究报告了全外显子组测序(WES)分析的病例和数据。我们报告了一例胰腺 UC-OGC,并进行了文献复习,为该肿瘤实体的分子特征提供了新的见解。

病例介绍

一名 31 岁男性因间歇性腹痛数月就诊,正电子发射断层扫描(PET)显示胰钩突处孤立性高代谢结节,可能为恶性疾病。根治性切除术后的病理检查显示与胰腺头部低分化腺癌相关的 UC-OGC。根治性手术后 7.4 个月疾病复发。随后的 WES 分析检测到 KRAS p.G12D(c.35G > A)和体细胞 BRCA2 p.R2896C(c.8686C > T)突变。该患者对铂类为基础的全身化疗无反应,病情迅速恶化。最终死亡,总生存期为 1 年。

结论

作为一种极罕见的肿瘤实体,UC-OGC 确实是一种独特的常规胰腺导管腺癌变异体,正如 WES 基因组分析所示。WES 的临床检查和分子分析可为 UC-OGC 提供潜在的治疗策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2f47/7318525/26f6c2d49b21/12876_2020_1351_Fig1_HTML.jpg

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