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IV期胃腺癌经新辅助治疗后完全缓解并合并壶腹腺癌:1例报告及文献复习

Gastric adenocarcinoma at stage IV with complete remission after neoadjuvant therapy concurrent with adenosquamous carcinoma of the ampulla of Vater: a case report and literature review.

作者信息

Li Shuo, Sun Mengqing, Wei Yingxin, Feng Yunlu, Chang Xiaoyan, You Yan, Liu Ziwen, Han Xianlin

机构信息

Department of General Surgery, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences, Beijing, 100730, China.

Department of Gastroenterology, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences, Beijing, 100730, China.

出版信息

BMC Surg. 2021 Apr 30;21(1):224. doi: 10.1186/s12893-021-01133-2.

Abstract

BACKGROUND

Adenosquamous carcinoma (ASC) of the ampulla of Vater (AmV) is exceedingly rare with more aggressive behavior and worse prognosis than adenocarcinoma. The finding of ASC at the AmV in combination to the gastric adenocarcinoma has never been reported in the literature before.

CASE PRESENTATION

An old lady was diagnosed as gastric adenocarcinoma at stage IV with enlargement of supraclavicular lymph nodes by gastroscopy and histopathological evaluation 3 years ago. Afterwards, the patient achieved complete remission after regular chemotherapy. However, the patient manifested yellow sclera and skin, choluria and clay colored stool 3 months ago. Preoperative contrast-enhanced CT, ERCP, MRCP, and PET/CT revealed the presence of an ampullary tumor. The patient then underwent laparoscopic radical gastrectomy and pancreaticoduodenectomy with regional lymph node dissection. Postoperative cytological analyses confirmed the diagnosis of gastric ulcer with complete response to neoadjuvant therapy and ASC at the AmV. The patient's postoperative outcome was uneventful.

CONCLUSION

Drawing firm conclusions about the diagnosis of ampullary ASC is difficult because of the difficulty in acquiring both adenocarcinoma and SCC components by fine needle biopsy. The rarity of ASC of the AmV coexistent with gastric carcinoma makes it difficult to elucidate their clinicopathological characteristics, therapeutic strategies and overall prognosis. Surgical resection still remains the main treatment method.

摘要

背景

壶腹腺癌(ASC)极为罕见,其行为比腺癌更具侵袭性,预后更差。壶腹处ASC合并胃腺癌的情况此前在文献中从未有过报道。

病例介绍

一位老年女性3年前经胃镜检查及组织病理学评估被诊断为IV期胃腺癌伴锁骨上淋巴结肿大。之后,患者在接受正规化疗后实现完全缓解。然而,3个月前患者出现巩膜及皮肤黄染、尿胆原阳性及陶土样大便。术前增强CT、内镜逆行胰胆管造影(ERCP)、磁共振胰胆管造影(MRCP)及正电子发射断层显像/计算机断层扫描(PET/CT)显示存在壶腹肿瘤。患者随后接受了腹腔镜根治性胃切除术及胰十二指肠切除术并进行了区域淋巴结清扫。术后细胞学分析证实为胃溃疡,对新辅助治疗完全缓解,且壶腹处为ASC。患者术后恢复顺利。

结论

由于细针穿刺活检难以同时获取腺癌和鳞癌成分,因此很难对壶腹ASC的诊断得出确切结论。壶腹ASC与胃癌并存的罕见性使得难以阐明其临床病理特征、治疗策略及总体预后。手术切除仍然是主要的治疗方法。

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