1例男婴双十二指肠闭锁的死亡过程。

Pub Date : 2020-01-01 Epub Date: 2020-02-07 DOI:10.1055/s-0039-3400488
Ahmed Elrouby, Ahmed Koraitim
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引用次数: 1

摘要

十二指肠多点闭锁是一种非常罕见的情况,在十二指肠的两个或三个部位闭锁。我们报告了一位新生儿男性患者,他在我们医院就诊时出现胆汁性呕吐、胎便无法通过、轻度腹胀和可触摸的上腹部肿块~ 1 × 1 cm。腹部x光片见微弱双泡。在剖腹探查术中,发现双十二指肠闭锁引起的十二指肠囊肿,并进行了典型的菱形十二指肠吻合术。术后对比研究显示造影剂进入远端肠。然而,患者在2周后死于未控制的败血症和肺炎。尽管多点十二指肠闭锁是一种罕见的情况,但它应被视为一种鉴别诊断,以避免遗漏病理。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Fatal Course of a Male Newborn with Double Duodenal Atresia.

Fatal Course of a Male Newborn with Double Duodenal Atresia.

Fatal Course of a Male Newborn with Double Duodenal Atresia.

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Fatal Course of a Male Newborn with Double Duodenal Atresia.

Multiple point duodenal atresia is an extremely rare condition with atretic segments in either two or three sites of the duodenum. We report a newborn male patient who presented to our institution with bilious vomiting, nonpassage of meconium, mild abdominal distension, and a palpable epigastric abdominal mass ∼1 × 1 cm. A faint double bubble was found on abdominal X-ray. On exploratory laparotomy, a duodenal cyst due to double duodenal atresia was found and a typical diamond-shaped duodeno-duodenostomy was created. A postoperative contrast study revealed passage of the contrast media into distal intestine. However, the patient died 2 weeks later due to uncontrolled sepsis and pneumonia. Despite the fact that multiple-point duodenal atresia is a rare condition, it should be considered as a differential diagnosis to avoid missed pathology.

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