Suppr超能文献

胃支气管源性囊肿:一例报告。

Bronchogenic cyst of the stomach: A case report.

作者信息

He Wen-Ting, Deng Jing-Yu, Liang Han, Xiao Jian-Yu, Cao Fu-Liang

机构信息

Department of Gastroenterology, Tianjin Medical University Cancer Institute and Hospital, National Clinical Research Center for Cancer, Key Laboratory of Cancer Prevention and Therapy, Tianjin, and Tianjin's Clinical Research Center for Cancer, Tianjin 300060, China.

Department of Radiology, Tianjin Medical University Cancer Institute and Hospital, National Clinical Research Center for Cancer, Key Laboratory of Cancer Prevention and Therapy, Tianjin, and Tianjin's Clinical Research Center for Cancer, Tianjin 300060, China.

出版信息

World J Clin Cases. 2020 Apr 26;8(8):1525-1531. doi: 10.12998/wjcc.v8.i8.1525.

Abstract

BACKGROUND

Gastric bronchogenic cysts (BCs) are extremely rare cystic masses caused by abnormal development of the respiratory system during the embryonic period. Gastric bronchial cysts are rare lesions first reported in 1956; as of 2019, only 37 cases are available in the MEDLINE/PubMed online databases. BCs usually have no clinical symptoms in the early stage, and their imaging findings also lack specificity. Therefore, they are difficult to diagnose before histopathological examination.

CASE SUMMARY

A 55-year-old woman presented at our hospital with intermittent epigastric pain. She had a slightly high level of serum carbohydrate antigen 72-4 (CA 72-4). Endoscopic ultrasound found that a cystic mass originated from the submucosa of the posterior gastric wall near the cardia, indicating a diagnosis of cystic hygroma of the stomach. Furthermore, a computed tomography scan demonstrated a quasi-circular cystic mass closely related to the lesser curvature of the gastric fundus with a low density. Because the imaging examinations did not suggest a malignancy and the patient required complete resection, she underwent laparoscopic surgery. As an intraoperative finding, this cystic lesion was located in the posterior wall of the fundus and contained some yellow viscous liquid. Finally, the pathologists verified that the cyst in the fundus was a gastric BC. The patient recovered well with normal CA 72-4 levels, and her course was uneventful at 10 mo.

CONCLUSION

This is a valuable report as it describes an extremely rare case of gastric BC. Moreover, this is the first case of BC to present with elevated CA 72-4 levels.

摘要

背景

胃支气管源性囊肿(BCs)是极其罕见的囊性肿物,由胚胎期呼吸系统发育异常所致。胃支气管囊肿是1956年首次报道的罕见病变;截至2019年,MEDLINE/PubMed在线数据库中仅有37例相关病例。BCs早期通常无临床症状,其影像学表现也缺乏特异性。因此,在组织病理学检查之前很难诊断。

病例摘要

一名55岁女性因间歇性上腹部疼痛前来我院就诊。她的血清糖类抗原72-4(CA 72-4)水平略高。内镜超声检查发现一个囊性肿物起源于贲门附近胃后壁的黏膜下层,提示胃淋巴管瘤的诊断。此外,计算机断层扫描显示一个类圆形囊性肿物,与胃底小弯关系密切,密度较低。由于影像学检查未提示恶性病变且患者需要完整切除,她接受了腹腔镜手术。术中发现,这个囊性病变位于胃底后壁,含有一些黄色黏稠液体。最后,病理学家证实胃底的囊肿为胃BC。患者恢复良好,CA 72-4水平正常,10个月来病情平稳。

结论

本报告具有重要价值,因为它描述了一例极其罕见的胃BC病例。此外,这是首例出现CA 72-4水平升高的BC病例。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c2ba/7190944/2f5814567860/WJCC-8-1525-g001.jpg

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验