[胰腺环形闭锁及肠道闭锁十二指肠闭锁的手术治疗[b]。

Néstor Gibrán López-Díaz, Edgar Fernando Oliver-García, Juan Carlos Núñez-Enríquez
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引用次数: 0

摘要

背景:与IIIb型肠闭锁相关的十二指肠闭锁是一种罕见的关联,文献报道的病例很少,考虑到即使是孤立的IIIb型肠闭锁病例也是一种挑战,这代表了一种手术挑战。目的是报道一例复杂肠道畸形的成功手术治疗,其特征是十二指肠阻塞继发于环状胰腺和IIIb型肠闭锁,根据定义,肠道旋转不良和存在Meckel憩室。临床病例:我们报告了一例新生儿因产前未诊断为十二指肠梗阻而被送至二级护理,根据Grosfeld分类导致环状胰腺十二指肠闭锁和IIIb型肠闭锁。十二指肠闭锁合并IIIb型肠闭锁是一种极其罕见的疾病,与环状胰腺相关的情况更是如此。考虑到小肠的长度较短,因此需要长时间的全肠外营养,这些病例是一个挑战。结论:对这一复杂肠道畸形的外科治疗使该病例术后发展良好,基于立即开始肠内喂养,短时间内需要全肠外营养,最终缩短了住院时间。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

[Surgical management of duodenal atresia due to annular pancreas and intestinal atresia IIIb].

[Surgical management of duodenal atresia due to annular pancreas and intestinal atresia IIIb].

[Surgical management of duodenal atresia due to annular pancreas and intestinal atresia IIIb].

[Surgical management of duodenal atresia due to annular pancreas and intestinal atresia IIIb].

Background: The presence of duodenal atresia related to type IIIb intestinal atresia is a rare association, with few cases reported in the literature, representing a surgical challenge considering that even isolated cases of type IIIb intestinal atresia are a challenge. The objective was to report the successful surgical management of a case of a complex intestinal malformation, characterized by duodenal occlusion secondary to annular pancreas and type IIIb intestinal atresia, with intestinal malrotation by definition and the presence of Meckel's diverticulum.

Clinical case: We present the case report of a newborn sent to the second level of care with a diagnosis of duodenal obstruction not diagnosed prenatally, which resulted in duodenal atresia due to annular pancreas and type IIIb intestinal atresia according to the Grosfeld classification. The presence of duodenal atresia with type IIIb intestinal atresia is an extremely rare condition, even more so associated with annular pancreas. These cases are a challenge considering the short length of the small intestine and its consequent need for total parenteral nutrition for a prolonged period.

Conclusions: The surgical management of this complex intestinal malformation resulted in a case with an adequate post-surgical evolution, based on the immediate start of enteral feeding with a short period of need for total parenteral nutrition that finally resulted in a short hospital stay.

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