Kano Taku, Iseki Masahiro, Aoki Shuichi, Mizuma Masamichi, Murakami Keigo, Kume Kiyoshi, Masamune Atsushi, Furukawa Toru, Kamei Takashi, Unno Michiaki
Department of Surgery, Tohoku University Graduate School of Medicine, 1-1 Seiryo-machi, Aoba-ku, Sendai, Miyagi, 980-8574, Japan.
Department of Investigative Pathology, Tohoku University Graduate School of Medicine, 1-1 Seiryo-machi, Aoba-ku, Sendai, Miyagi, 980-8574, Japan.
Clin J Gastroenterol. 2025 Aug 6. doi: 10.1007/s12328-025-02193-0.
FGFR2 fusions and rearrangements are genetic abnormalities commonly observed in intrahepatic cholangiocarcinoma. A 42-year-old woman with a history of breast cancer presented to our hospital with jaundice. The patient was clinically diagnosed with distal cholangiocarcinoma (DCCA), and underwent pancreaticoduodenectomy. The tumor extensively invaded the pancreatic head, and intraductal spread was found in a branch of the pancreatic duct. Therefore, the patient was postoperatively diagnosed with pancreatic ductal adenocarcinoma (PDAC). Multiple lung metastases appeared 51 months after surgical resection. Partial lung resection confirmed histologically that the lung metastasis originated from PDAC. Furthermore, comprehensive genomic profiling (CGP) of lung resection specimens revealed FGFR2-SYCP1 fusion. However, common genetic alterations in PDAC, such as KRAS, SMAD4, TP53, and CDKN2A, were not detected in CGP. A re-evaluation of the resected pancreatic tissue showed that the histological features were possible for DCCA; however, it was difficult to make a conclusive diagnosis. Based on CGP analysis, the patient is currently receiving futibatinib, and the lung metastatic lesions have shrunk or partly disappeared. CGP can assist in selecting an appropriate therapeutic strategy when histological differentiation between DCCA and PDAC is challenging.
FGFR2融合和重排是肝内胆管癌中常见的基因异常。一名有乳腺癌病史的42岁女性因黄疸前来我院就诊。该患者临床诊断为远端胆管癌(DCCA),并接受了胰十二指肠切除术。肿瘤广泛侵犯胰头,在胰管分支中发现了导管内扩散。因此,该患者术后被诊断为胰腺导管腺癌(PDAC)。手术切除51个月后出现多处肺转移。部分肺切除术后组织学证实肺转移源自PDAC。此外,肺切除标本的综合基因组分析(CGP)显示存在FGFR2-SYCP1融合。然而,在CGP中未检测到PDAC常见的基因改变,如KRAS、SMAD4、TP53和CDKN2A。对切除的胰腺组织进行重新评估显示,其组织学特征可能符合DCCA;然而,很难做出明确诊断。基于CGP分析,该患者目前正在接受futibatinib治疗,肺转移病灶已缩小或部分消失。当DCCA和PDAC的组织学鉴别具有挑战性时,CGP有助于选择合适的治疗策略。