Acute abdomen due to Meckel's diverticulitis with synchronous inflammatory myofibroblastic tumor in the terminal ileum: A case report.

Burak Dinçer, Sinan Ömeroğlu, Onur Güven, Mustafa Fevzi Celayir, Uygar Demir
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Abstract

Meckel's diverticulum (MD) is the most common congenital anomaly of the gastrointestinal system, occurring in approximately 2% of the population. It is rare for MD to be symptomatic or complicated in adulthood. In this case report, we describe a patient who was admitted to the clinic with Meckel's diverticulitis, which had fistulized to the anterior abdominal wall, and was incidentally found to have an ileal inflammatory myofibroblastic tumor (IMT) on radiological imaging. A 46-year-old male patient presented to the emergency department with abdominal pain. Physical examination revealed localized guarding on the right side of the umbilicus. Blood tests showed elevated acute-phase reactants, including a white blood cell count of 13,800/µL, and C-reactive protein (CRP) level of 165 mg/L. Abdominal computed tomography demonstrated Meckel's diverticulitis fistulizing to the anterior abdominal wall and a polypoid structure in the ileum distal to the MD. The patient underwent emergency surgery, during which segmental ileal resection and ileocolic anastomosis were performed. On the fourth postoperative day, the patient developed an anastomotic leak. Relaparotomy, right hemicolectomy with end ileostomy, and mucous fistula creation were subsequently performed. Pathological examination of the resected ileum from the initial surgery revealed a benign IMT distal to the MD. The patient was discharged on the 40th postoperative day after developing a surgical site infection following the second surgery. The end ileostomy was closed six months later. In this case, it appears that the ileal IMT located distal to the MD may have caused intermittent intestinal obstruction, fecal stasis, and the development of Meckel's diverticulitis. Furthermore, a detailed examination of the patient's history, laboratory results, and radiologic tests may contribute to the detection of incidental pathologies and influence treatment choices.

梅克尔憩室炎引起的急腹症伴回肠末端同步炎性肌纤维母细胞瘤:病例报告。
梅克尔憩室(MD)是最常见的先天性胃肠道系统畸形,发病率约占总人口的 2%。成年后出现症状或并发症的梅克尔憩室并不多见。在本病例报告中,我们描述了一名因梅克尔憩室炎入院的患者,该憩室炎已瘘至前腹壁,在放射影像学检查中意外发现其患有回肠炎性肌纤维母细胞瘤(IMT)。一名46岁的男性患者因腹痛到急诊科就诊。体格检查发现患者脐部右侧有局部疼痛。血液检查显示急性期反应物升高,其中白细胞计数为 13,800 个/微升,C 反应蛋白(CRP)水平为 165 毫克/升。腹部计算机断层扫描显示,梅克尔憩室炎瘘管延伸至前腹壁,MD远端回肠有息肉样结构。患者接受了急诊手术,在手术过程中进行了回肠节段切除和回结肠吻合术。术后第四天,患者出现吻合口漏。随后进行了再切断术、右半结肠切除术和回肠末端造口术,并造了粘液瘘。对初次手术切除的回肠进行病理检查后发现,MD远端有一个良性IMT。患者在第二次手术后出现手术部位感染,于术后第40天出院。六个月后关闭了末端回肠造口。在这个病例中,位于 MD 远端的回肠 IMT 似乎可能导致了间歇性肠梗阻、粪便淤积和梅克尔憩室炎的发生。此外,对患者病史、实验室结果和放射检查的详细检查可能有助于发现偶发病变并影响治疗选择。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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