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十二指肠脂肪瘤的诊断与治疗:一项系统综述及病例报告

Diagnosis and Treatment of Duodenal Lipoma: A Systematic Review and a Case Report.

作者信息

Pei Mao Wei, Hu Ming Rong, Chen Wen Bin, Qin Chao

机构信息

Assistant Professor, Department of General Surgery, The Affiliated Hospital of Hangzhou Normal University, HangZhou, Zhejiang, China.

Professor, Department of General Surgery, The Affiliated Hospital of Hangzhou Normal University, HangZhou, Zhejiang, China.

出版信息

J Clin Diagn Res. 2017 Jul;11(7):PE01-PE05. doi: 10.7860/JCDR/2017/27748.10322. Epub 2017 Jul 1.

Abstract

INTRODUCTION

Duodenal lipoma is very rare with limited case reports present in literature. Owing to recent advances in endoscopy and modern imaging techniques, more cases are being diagnosed and treated. However, no systematic study of duodenal lipomas has been reported.

AIM

To study the diagnosis and treatment of duodenal lipoma in a female patient and review the relative literatures to enhance the knowledge of it.

MATERIALS AND METHODS

A literature search for 'duodenal lipoma' was performed on PubMed. Papers published from 1948 to 2016 in the English language were identified. Each article was then read in detail and analysed for clinical data, imaging features, diagnosis and therapy. Also, we hereby present a case of upper gastrointestinal obstruction secondary to multiple duodenal lipomas in a 67-year-old woman. The patient underwent a limited bowel resection with an uneventful recovery.

RESULTS

Literature review demonstrated 59 cases of duodenal lipoma, which indicate that duodenal lipomas are rare to occur but commonly found in the second part. The peak of incidence seems to be around the fifth and seventh decade of life. Duodenal lipomas may present as gastrointestinal bleeding, abdominal pain, obstruction or upper abdominal fullness. CT, MRI, Endoscopic Ultrasound (EUS), endoscopy are highly accurate diagnostic tools. The disease could be managed by endoscopy or surgery.

CONCLUSION

Our review of literature indicated duodenal lipoma is extremely rare. The symptoms are nonspecific and CT is the first choice for diagnosis. The treatment depends on the patient's condition as well as the size and position of the tumour.

摘要

引言

十二指肠脂肪瘤非常罕见,文献中仅有有限的病例报告。由于内镜检查和现代成像技术的最新进展,更多病例得以诊断和治疗。然而,尚未有关于十二指肠脂肪瘤的系统研究报告。

目的

研究一名女性患者十二指肠脂肪瘤的诊断和治疗,并回顾相关文献以增进对此病的了解。

材料与方法

在PubMed上对“十二指肠脂肪瘤”进行文献检索。确定了1948年至2016年以英文发表的论文。然后详细阅读每篇文章,并分析其临床数据、影像学特征、诊断和治疗方法。此外,我们在此报告一例67岁女性因多发性十二指肠脂肪瘤继发上消化道梗阻的病例。该患者接受了有限肠段切除术,术后恢复顺利。

结果

文献回顾显示有59例十二指肠脂肪瘤病例,表明十二指肠脂肪瘤虽罕见,但常见于十二指肠第二部。发病高峰似乎在生命的第五和第七个十年左右。十二指肠脂肪瘤可能表现为胃肠道出血、腹痛、梗阻或上腹部饱胀感。CT、MRI、内镜超声(EUS)、内镜检查是高度准确的诊断工具。该病可通过内镜或手术治疗。

结论

我们的文献回顾表明十二指肠脂肪瘤极为罕见。症状不具特异性,CT是诊断的首选。治疗取决于患者的病情以及肿瘤的大小和位置。

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