Rare presentation of idiopathic duodenoduodenal intussusception

被引:10
作者
Loo, G. H. [1 ]
Abu Zeid, W. M. Mohamad [1 ]
Lim, S. L. [1 ]
Ismail, A. M. [2 ]
机构
[1] Bintulu Hosp, Gen Surg, Bintulu City, Bintulu, Malaysia
[2] Hosp Umum Sarawak, Pathol Dept, Kuching, Sarawak, Malaysia
关键词
Duodenal intussusception; Duodenoduodenal intussusception; Idiopathic duodenal intussusception;
D O I
10.1308/rcsann.2017.0104
中图分类号
R61 [外科手术学];
学科分类号
摘要
Enteroenteric intussusception is a condition in which the full-thickness bowel wall becomes telescoped into the lumen of distal bowel. Intussusception in adult occurs infrequently and varies from childhood intussusception, particularly in its presentation, aetiology and treatment. Duodenoduodenal intussusception is rare because the duodenum is fixed in the retroperitoneal position. It usually occurs secondary to tumour, lipoma, Brunner's gland hamartomatous polyp or adenoma. The diagnosis in adults is usually made at laparotomy, where presentation is with intestinal obstruction. In non-emergency presentation, it may be difficult to arrive at an accurate diagnosis as symptoms may be vague, self-limiting intermittent abdominal pain. Clinical examinations and investigations may not be conclusive and another working diagnosis such as irritable bowel syndrome would be made. We describe a case where a patient initially presented with symptoms mimicking pancreatitis but his symptoms persisted over the course of 2 weeks. When a laparotomy was performed, duodenoduodenal intussusception was discovered and confirmed with histopathology. In this case, a discernible leading point could not be identified.
引用
收藏
页码:E188 / E190
页数:3
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