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Strangulated Umbilical Littre's Hernia In A Paediatric Patient: A Case Report

机译:小儿患者脐带绞窄疝气:一例报告

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Littre's hernia is rare and often only discovered when complications arise. We report a case of strangulated umbilical Littre's hernia in a child. The patient was a 2-year old boy admitted for painful umbilical swelling. There was no fever. A surgical exploration found a strangulated Meckel's diverticulum. We proceeded with an ileum resection. The postoperative course was normal. Introduction Meckel's diverticulum (MD) is the most common anomaly of the gastrointestinal tract. It occurs in 0,3 to 3% of the general population [1]. It is often discovered in surgery because of some complications. Any hernia containing MD is named Littre's hernia. Strangulated umbilical Littre's hernia is very rare. We report a case with this condition. Case report A 2-year old boy was admitted to the Emergency Unit of the Regional Hospital of Thiès with a 10 hours history of painful umbilical swelling with vomiting. The Child did not have any episode of gastrointestinal bleeding or fever. Physical examination revealed an irreducible painful umbilical swelling. The laboratory tests were normal. No imaging examination was done. Under general anesthesia, the contents of the hernial sac were found to be a loop of ileum with a diverticulum on the antimesenteric side. There was no gangrenous tissue. There was also an adhesion between the diverticulum and the hernial sac and a hematoma on the mesenteric side (figure 1). A resection was performed to remove 10 cm of the small bowel on both sides of the MD followed by an immediate end-to-end anastomosis. The postoperative course was normal. The boy was discharged 7 days after the surgery in good clinic condition. On his 3 months follow-up he was well with no complaints. Histological study confirmed MD with heterotopic gastric mucosa without mucosal infarctions.
机译:Littre疝很罕见,通常仅在并发症发生时才发现。我们报告了一名儿童勒索性绞窄疝的病例。该患者是一名2岁男孩,因脐带肿胀而入院。没有发烧。外科手术探查发现绞窄的梅克尔憩室。我们进行了回肠切除术。术后病程正常。简介梅克尔憩室(MD)是胃肠道最常见的异常。它发生在总人口的0.3%至3%[1]中。由于一些并发症,它经常在外科手术中发现。任何包含MD的疝都称为Littre疝。绞窄的脐Littre疝很罕见。我们报告了这种情况的情况。病例报告一名2岁男孩因Thiès地区医院急诊科入院,有10个小时的疼痛性脐带肿胀呕吐病史。儿童没有胃肠道出血或发烧的任何发作。体格检查显示无法缓解的痛苦脐带肿胀。实验室检查正常。没有影像学检查。在全身麻醉下,发现疝囊的内容物是回肠loop回,在触角不全侧有憩室。没有坏疽组织。憩室与疝囊之间以及肠系膜一侧的血肿之间也存在粘连(图1)。进行切除术以去除MD两侧10 cm的小肠,然后立即进行端到端吻合。术后病程正常。手术后7天,男孩出院,临床状况良好。在3个月的随访中,他表现良好,没有任何抱怨。组织学研究证实MD为异位胃粘膜,无粘膜梗塞。

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