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年轻女性中表现为左肾上腺囊肿的延迟出现的胃重复囊肿:一例报告及文献综述

Delayed Presenting Gastric Duplication Cyst Mimicking a Left Adrenal Cyst in a Young Female: A Case Report with a Literature Review.

作者信息

Bapir Rawa, Qader Deedar, Gharib Dana, Tahir Soran, Abdullah Ari, Asaad Hoshmand, Ahmed Shaho, Ali Hemn, Abdullah Hiwa, Ahmed Sasan, Hussein Kakamad Fahmi, Aghaways Ismaeel

机构信息

Smart Health Tower, Sulaimani, Iraq.

Department of Urology, Sulaimani Surgical Teaching Hospital, Sulaimani, Iraq.

出版信息

Case Rep Gastroenterol. 2024 Mar 22;18(1):153-160. doi: 10.1159/000537972. eCollection 2024 Jan-Dec.

Abstract

INTRODUCTION

Gastric duplication cyst (GDC) is a rare congenital anomaly of the gastrointestinal tract. Though GDC is often misdiagnosed, misidentification as an adrenal cyst has rarely been reported. Herein, we report a case of GDC in a young female mimicking an adrenal cyst.

CASE PRESENTATION

A 17-year-old female presented with chronic epigastric pain, nausea, and intermittent vomiting. Physical examinations revealed mild tenderness in the epigastric region. Esophagogastroduodenoscopy showed no abnormality. Ultrasound, contrast-enhanced computed tomography scan, and MRI of the abdomen and pelvis showed an oval-shaped left adrenal cystic lesion measuring 33 × 26 mm. Preoperative blood investigations and hormonal assessments were normal. Laparoscopy showed that the cyst originated from the greater curvature of the stomach. The left adrenal gland was normal. After an intraoperative consultation with a gastrointestinal surgeon, a wedge resection of the cyst was performed. Histopathology confirmed the gastric duplication cyst.

CONCLUSION

GDCs are rare congenital malformations that may become symptomatic during adulthood. They can mimic adrenal cysts and lead to misdiagnosis.

摘要

引言

胃重复囊肿(GDC)是一种罕见的胃肠道先天性异常。尽管GDC常被误诊,但误诊为肾上腺囊肿的情况鲜有报道。在此,我们报告一例年轻女性的GDC,其表现类似肾上腺囊肿。

病例介绍

一名17岁女性因慢性上腹部疼痛、恶心和间歇性呕吐就诊。体格检查发现上腹部轻度压痛。食管胃十二指肠镜检查未发现异常。腹部和盆腔的超声、增强计算机断层扫描及磁共振成像显示左肾上腺有一个椭圆形囊性病变,大小为33×26mm。术前血液检查和激素评估均正常。腹腔镜检查显示囊肿起源于胃大弯。左肾上腺正常。在与胃肠外科医生进行术中会诊后,对囊肿进行了楔形切除。组织病理学证实为胃重复囊肿。

结论

GDC是罕见的先天性畸形,成年期可能出现症状。它们可类似肾上腺囊肿并导致误诊。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7a9d/10959546/5e77c573ce01/crg-2024-0018-0001-537972_F01.jpg

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