自发性梅克尔憩室穿孔:新生儿急腹症的罕见病因。

IF 0.6 Q3 MEDICINE, GENERAL & INTERNAL
Shoham Majumder, Aisha Naaz, Chinmay Chetan, Saikat Patra
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引用次数: 0

摘要

梅克尔憩室是一种先天性胃肠道畸形,在新生儿年龄组中很少被发现。在这里,我们提出一个新生儿谁提出给我们呼吸窘迫和急腹症。x光片显示气腹。剖腹探查发现梅克尔憩室尖端穿孔伴粪性腹膜炎。行楔形切除吻合。未见异位或发育不良组织。婴儿病情好转,出院时开始纯母乳喂养。本病例强调了一种罕见的情况,这种情况很少有症状,特别是在新生儿时期。虽然最常见的临床表现包括肠梗阻、炎症或出血,但我们的患者在没有任何明确的易感危险因素的情况下表现为憩室自发性穿孔。这个病例强调了在突发性急腹症病例中高度怀疑的重要性,因为及时诊断和处理可能会有良好的结果。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Spontaneously perforated Meckel's diverticulum: a rare cause of neonatal acute abdomen.

Meckel's diverticulum, a congenital gastrointestinal malformation, is seldom detected in the neonatal age group. Here, we present a neonate who presented to us with respiratory distress and acute abdomen. An X-ray showed pneumoperitoneum. Exploratory laparotomy revealed perforation at the tip of Meckel's diverticulum with faecal peritonitis. Wedge resection and anastomosis were performed. There were no heterotopic or dysplastic tissues. The baby improved and was discharged on exclusive breastfeeding. This case highlights a rare condition, which is rarely symptomatic, particularly in the neonatal period. While the most common clinical presentations include intestinal obstruction, inflammation or bleeding, our patient presented with a spontaneous perforation of the diverticulum in the absence of any clear predisposing risk factors. This case highlights the importance of a high index of suspicion in cases of sudden acute abdomen, as prompt diagnosis and management may have a good outcome.

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来源期刊
BMJ Case Reports
BMJ Case Reports Medicine-Medicine (all)
CiteScore
1.40
自引率
0.00%
发文量
1588
期刊介绍: BMJ Case Reports is an important educational resource offering a high volume of cases in all disciplines so that healthcare professionals, researchers and others can easily find clinically important information on common and rare conditions. All articles are peer reviewed and copy edited before publication. BMJ Case Reports is not an edition or supplement of the BMJ.
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