空肠重叠表现为穿孔性腹膜炎:一例罕见的老年女性先天性畸形的并发症

Shubha Gupta, Pramod Meena, Aviral Srivastava, R. Anand, R. Khanna, R. Meena, S. Mishra
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引用次数: 0

摘要

肠道重复是一种罕见的先天性畸形,通常在儿童早期发现或出现症状,在成人中很少报道。回肠是最常见的部位,空肠很少受累。特征通常是非特异性的,因此难以诊断。超声检查通常是首选的成像方法。手术方式取决于表现。我们提出一个病例的成年女性提出穿孔腹膜炎。术中发现在肠系膜边缘约6厘米长的相通的空肠管重复,穿孔累及重复段和正常空肠。切除空肠重复段并吻合。本报告提出了对肠道重复及其临床表现的进一步了解,并强调了这种实体如何以及为什么在术前被遗漏,并成为术中惊喜。
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Jejunal duplication presenting with perforation peritonitis: Complication of a rare congenital malformation in an elderly female
Intestinal duplication is a rare congenital malformation that is usually detected or becomes symptomatic in early paediatric age and is rarely reported in adults. The ileum is the most frequent site, while jejunum is rarely involved. Features are often nonspecific, hence difficult to diagnose. Ultrasonography is often preferred imaging method. The surgical procedure is determined depending on the presentation. We present a case of an adult female presenting with perforation peritonitis. Intraoperatively, approximately 6 cm length communicating jejunal tubular duplication over the mesenteric margin was found, with perforation involving the duplication segment and normal jejunum. Resection of jejunal duplication segment and anastomosis was carried out. This presentation proposed further insight into enteric duplication and their clinical presentations, along with emphasis on how and why this entity was missed preoperatively and came out to be an intra-operative surprise.
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