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成人罕见的回盲部肠套叠:一例诊断与治疗的病例报告

Uncommon Ileo-Cecal Intussusception in Adults: A Case Report of Diagnosis and Management.

作者信息

Ngwengi Yembu, Beugheum Christian, Ottou Christian, Mindjeme Benjamin Freddy, Soh Jacqueline, Ngoulla Roger

机构信息

Department of Emergency Medicine, Marie O Polyclinic, Douala, Cameroon.

Faculty of Medicine and Pharmaceutical Sciences, University of Douala, Douala, Cameroon.

出版信息

Am J Case Rep. 2025 Aug 20;26:e946853. doi: 10.12659/AJCR.946853.

Abstract

BACKGROUND This report describes the case of a 36-year-old man presenting with severe abdominal pain and small-bowel obstruction due to idiopathic ileo-cecal intussusception. Intussusception refers to the telescoping or folding of a segment of bowel into the section distal to it. It is one of the main differentials of small-bowel obstruction in the pediatric population, but remains exceedingly rare in adults. Intussusception in adults is generally associated with organic masses of the digestive tract, especially tumors, which act as lead points that drag the proximal bowel into a more distal segment. It is extremely uncommon to find intussusception in an adult patient with no obvious underlying bowel pathology. CASE REPORT We report a case of ileo-cecal intussusception in an adult patient that yielded no underlying bowel anomaly on surgical exploration and pathology. The patient, a 36-year-old man, presented with severe abdominal pain and was diagnosed with intussusception through computed tomography (CT) scanning. Surgical resection and anastomoses of the bowel were subsequently performed when medical therapy failed. The patient experienced diarrhea and vitamin-deficient neuropathy a month after surgery, which was diagnosed as short bowel syndrome, and which resolved with appropriate medical care. CONCLUSIONS Intussusception, while rare in adult patients, is possible even without underlying bowel disease. However, a thorough surgical exploration and proper pathology analysis are essential to confidently exclude other gut anomalies. Clinicians should be aware of possible complications like short bowel syndrome if the surgical approach is used and a significant amount of intestine is resected.

摘要

背景 本报告描述了一名36岁男性患者,因特发性回盲肠套叠出现严重腹痛和小肠梗阻。套叠是指一段肠管套入其远端的肠段。它是儿科人群小肠梗阻的主要鉴别诊断之一,但在成人中仍然极为罕见。成人套叠通常与消化道的器质性肿物有关,尤其是肿瘤,这些肿物作为引导点将近端肠管拖入更远端的肠段。在没有明显潜在肠道病变的成年患者中发现套叠极为罕见。病例报告 我们报告一例成年患者的回盲肠套叠,手术探查和病理检查未发现潜在的肠道异常。该患者为一名36岁男性,因严重腹痛就诊,通过计算机断层扫描(CT)被诊断为套叠。药物治疗失败后,随后进行了肠段的手术切除和吻合。患者术后一个月出现腹泻和维生素缺乏性神经病变,被诊断为短肠综合征,经适当的医疗护理后症状缓解。结论 套叠在成年患者中虽然罕见,但即使没有潜在的肠道疾病也有可能发生。然而,进行全面的手术探查和适当的病理分析对于可靠地排除其他肠道异常至关重要。如果采用手术方法并切除大量肠段,临床医生应意识到可能出现的并发症,如短肠综合征。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/499c/12376928/a411f0095785/amjcaserep-26-e946853-g001.jpg

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