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2
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Perforated meckel's diverticulum misdiagnosed as a urinary tract infection in an 11-year-old adolescent: case report of a rare differential diagnosis.一名11岁青少年的梅克尔憩室穿孔被误诊为尿路感染:罕见鉴别诊断的病例报告
Patient Saf Surg. 2025 Jul 3;19(1):20. doi: 10.1186/s13037-025-00443-1.
2
Adult intussusception associated with mesenteric Meckel's diverticulum and antimesenteric ileal polyp.成人肠套叠合并肠系膜梅克尔憩室及对系膜缘回肠息肉。
BMJ Case Rep. 2019 Sep 18;12(9):e230612. doi: 10.1136/bcr-2019-230612.

本文引用的文献

1
Perforated mesenteric Meckel's diverticulum in an adult: a real variant?成人肠系膜穿孔性梅克尔憩室:一种真实的变异?
J Surg Case Rep. 2015 Sep 1;2015(9):rjv115. doi: 10.1093/jscr/rjv115.
2
Meckel's diverticulum at uncommon mesenteric location.位于罕见肠系膜位置的梅克尔憩室。
J Indian Assoc Pediatr Surg. 2013 Jul;18(3):127-8. doi: 10.4103/0971-9261.116052.
3
Mesenteric localization of Meckel's diverticulum.
Turk J Gastroenterol. 2013;24(2):189-90. doi: 10.4318/tjg.2013.0485.
4
An uncommon location of Meckel's diverticulum or small intestine duplication? Case report and literature review.梅克尔憩室或小肠重复畸形的罕见部位?病例报告及文献综述。
Pol Przegl Chir. 2011 Aug;83(8):457-60. doi: 10.2478/v10035-011-0071-z.
5
Perforated Meckel's diverticulitis on the mesenteric side: MDCT findings.肠系膜侧穿孔性梅克尔憩室炎:多层螺旋CT表现
Abdom Imaging. 2012 Apr;37(2):288-91. doi: 10.1007/s00261-011-9733-x.
6
Meckel's diverticulum: a review. Meckel's 憩室:综述。
Clin Anat. 2011 May;24(4):416-22. doi: 10.1002/ca.21094. Epub 2011 Feb 14.
7
Mesenteric Meckel's diverticulum: a case report.肠系膜梅克尔憩室:一例报告
Acta Chir Belg. 2009 Jul-Aug;109(4):510-2. doi: 10.1080/00015458.2009.11680472.
8
An uncommon variant of Meckel's diverticulum.梅克尔憩室的一种罕见变异型。
Can J Surg. 2008 Apr;51(2):E46-7.
9
Complications of Meckel's diverticula in adults.成人梅克尔憩室的并发症。
Can J Surg. 2006 Oct;49(5):353-7.
10
Rare mesenteric location of Meckel's diverticulum, a forgotten entity: a case study aboard USS Kitty Hawk.梅克尔憩室罕见的肠系膜位置:一个被遗忘的实体——“小鹰号”航母上的病例研究
Am Surg. 2004 Nov;70(11):985-8.

肠系膜梅克尔憩室:小肠套叠的罕见病因。

Mesenteric Meckel's diverticulum: an unusual cause of small bowel intussusception.

作者信息

Abbas Syed Hussain, Akbari Khalid, Mason John, Booth Michael

机构信息

Royal Berkshire Hospital, Reading, Berkshire, UK.

出版信息

BMJ Case Rep. 2016 Apr 8;2016:bcr2016214830. doi: 10.1136/bcr-2016-214830.

DOI:10.1136/bcr-2016-214830
PMID:27060074
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4840622/
Abstract

Meckel's diverticulum (MD) is the commonest congenital anomaly of the small intestine, affecting 1-4% of the population. Cardinal features emphasise an antimesenteric location two feet proximal to the ileocaecal valve, with a separate mesenteric blood supply and involvement of all layers of the small intestine. However, reports of MD arising from the mesenteric border of the small intestine are rare in the surgical literature. This report examines the case of a 45-year-old woman presenting with a 6-month history of episodic central abdominal pain and microcytic anaemia who underwent an elective diagnostic laparoscopy as initial CT findings were inconclusive. Intraoperatively, she was found to have small bowel intussusception approximately 40 cm proximal to the ileocaecal valve. Macroscopic examination of the resected small bowel segment revealed a mesenteric outpouching that was confirmed as mesenteric MD on histopathological analysis. Postoperatively, the patient recovered with no surgical complications and full symptom resolution.

摘要

梅克尔憩室(MD)是小肠最常见的先天性异常,影响1% - 4%的人群。主要特征为位于回盲瓣近端两英尺处的肠系膜对侧位置,有独立的肠系膜血液供应且累及小肠全层。然而,小肠系膜缘起源的MD在外科文献中报道较少。本报告探讨了一名45岁女性的病例,该患者有6个月发作性中腹部疼痛和小细胞贫血病史,因初始CT检查结果不明确而接受了选择性诊断性腹腔镜检查。术中发现她在回盲瓣近端约40厘米处发生小肠套叠。对切除的小肠段进行宏观检查发现一个系膜憩室,经组织病理学分析证实为系膜梅克尔憩室。术后,患者康复,无手术并发症,症状完全缓解。