Suppr超能文献

年轻患者的巨大胃支气管源性囊肿:一例报告并文献复习

Young patient with a giant gastric bronchogenic cyst: A case report and review of literature.

作者信息

Lu Xu-Ren, Jiao Xu-Guang, Sun Qi-Hang, Li Bo-Wen, Zhu Qing-Shun, Zhu Guang-Xu, Qu Jian-Jun

机构信息

School of Clinical Medicine, Shandong Second Medical University, Weifang 261000, Shandong Province, China.

Department of Gastrointestinal Surgery Medical Center, The First Affiliated Hospital, Shandong Second Medical University, Weifang 261000, Shandong Province, China.

出版信息

World J Clin Cases. 2024 May 6;12(13):2254-2262. doi: 10.12998/wjcc.v12.i13.2254.

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 that were first reported in 1956; as of 2023, only 33 cases are available in the PubMed online database. BCs usually have no clinical symptoms in the early stage, and imaging findings also lack specificity. Therefore, they are difficult to diagnose before histopathological examination.

CASE SUMMARY

A 34-year-old woman with respiratory distress presented at our hospital. Endoscopic ultrasound revealed an anechoic mass between the spleen, left kidney and gastric fundus, with hyperechogenic and soft elastography textures and with a size of approximately 6.5 cm × 4.0 cm. Furthermore, a computed tomography scan demonstrated high density between the posterior stomach and the spleen and the left kidney, with uniform internal density and a small amount of calcification. The maximum cross section was approximately 10.1 cm × 6.1 cm, and the possibility of a cyst was high. Because the imaging findings did not suggest a malignancy and because the patient required complete resection, she underwent laparotomy surgery. Intraoperatively, this cystic lesion was found to be located in the posterior wall of the large curvature of the fundus and was approximately 8 cm × 6 cm in size. Finally, the pathologists verified that the cyst in the fundus was a gastric BC. The patient recovered well, her symptoms of chest tightness disappeared, and the abdominal drain was removed on postoperative day 6, after which she was discharged on day 7 for 6 months of follow-up. She had no tumor recurrence or postoperative complications during the follow-up.

CONCLUSION

This is a valuable report as it describes an extremely rare case of gastric BC. Moreover, this was a very young patient with a large BC in the stomach.

摘要

背景

胃支气管源性囊肿(BCs)是极为罕见的囊性肿物,由胚胎期呼吸系统发育异常所致。胃支气管囊肿是罕见病变,于1956年首次报道;截至2023年,在PubMed在线数据库中仅有33例相关病例。BCs早期通常无临床症状,影像学表现也缺乏特异性。因此,在组织病理学检查前难以诊断。

病例摘要

一名34岁呼吸窘迫的女性到我院就诊。内镜超声显示脾脏、左肾与胃底之间有一无回声肿物,弹性成像质地为高回声且柔软,大小约为6.5 cm×4.0 cm。此外,计算机断层扫描显示胃后壁与脾脏及左肾之间密度增高,内部密度均匀,有少量钙化。最大横截面约为10.1 cm×6.1 cm,囊肿可能性大。因影像学表现未提示恶性且患者需要完整切除,故行剖腹手术。术中发现该囊性病变位于胃底大弯后壁,大小约为8 cm×6 cm。最后,病理学家证实胃底囊肿为胃BC。患者恢复良好,胸闷症状消失,术后第6天拔除腹腔引流管,第7天出院并进行6个月随访。随访期间无肿瘤复发及术后并发症。

结论

本报告很有价值,因为它描述了一例极为罕见的胃BC病例。此外,这是一名非常年轻且胃内有大BC的患者。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c823/11129127/1039ad071c83/WJCC-12-2254-g001.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验