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新生儿苹果皮样小肠闭锁合并孤立性空肠重复囊肿——1例极其罕见的病例报告及简要综述

Apple-Peel Intestinal Atresia Along with Isolated Jejunal Duplication Cyst in a Newborn - An Extremely Rare Case Report and Brief Review.

作者信息

Tripathy Prasanta Kumar, Pattnaik Kaumudee, Jena Pradip Kumar, Mohanty Hiranya Kishor

机构信息

Assistant Professor, Deparment of Paediatric Surgery, SCB Medical College, Cuttack, Odisha, India.

Associate Professor, Deparment of Pathology, SCB Medical College, Cuttack, Odisha, India.

出版信息

J Clin Diagn Res. 2017 Jun;11(6):SD01-SD02. doi: 10.7860/JCDR/2017/26900.10123. Epub 2017 Jun 1.

DOI:10.7860/JCDR/2017/26900.10123
PMID:28764258
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5535448/
Abstract

Apple-peel type of intestinal atresia and non-communicating jejunal duplication cyst are rare congenital malformations. The coexistence is not reported in English literature. A five-day-old female neonate having intestinal obstruction and was found to have both the anomalies during laparotomy and was successfully managed. Being an extremely uncommon association between two congenital anomalies of gastrointestinal tract and surgical emergencies, it is reported with review of relevant literature.

摘要

苹果皮样肠闭锁和非交通性空肠重复囊肿是罕见的先天性畸形。英文文献中未报道过两者并存的情况。一名五天大的女性新生儿患有肠梗阻，在剖腹手术中发现同时存在这两种异常，并成功得到治疗。鉴于这是胃肠道两种先天性异常与外科急症之间极为罕见的关联，现结合相关文献进行报道。

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Apple-Peel Intestinal Atresia Along with Isolated Jejunal Duplication Cyst in a Newborn - An Extremely Rare Case Report and Brief Review.新生儿苹果皮样小肠闭锁合并孤立性空肠重复囊肿——1例极其罕见的病例报告及简要综述
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引用本文的文献

1
[Therapeutic experience of type Ⅲ-b congenital intestinal atresia].[Ⅲ - b型先天性肠闭锁的治疗经验]
Zhejiang Da Xue Xue Bao Yi Xue Ban. 2019 Jul 25;48(5):487-492. doi: 10.3785/j.issn.1008-9292.2019.10.04.

本文引用的文献

1
Isolated Jejunal Duplication Cyst Associated with Intestinal Malrotation in a Newborn.新生儿孤立性空肠重复囊肿合并肠旋转不良
J Neonatal Surg. 2016 Oct 10;5(4):63. doi: 10.21699/jns.v5i4.455. eCollection 2016 Oct-Dec.
2
Histomorphological Features of Intestinal Atresia and its Clinical Correlation.肠闭锁的组织形态学特征及其临床相关性
J Clin Diagn Res. 2015 Nov;9(11):EC26-9. doi: 10.7860/JCDR/2015/13320.6838. Epub 2015 Nov 1.
3
Pseudo double bubble: jejunal duplication mimicking duodenal atresia on prenatal ultrasound.假性双泡征：产前超声检查中，空肠重复畸形酷似十二指肠闭锁。
J Neonatal Surg. 2013 Oct 1;2(4):42. eCollection 2013 Oct-Dec.
4
Intestinal atresia.肠闭锁
Indian J Pediatr. 2000 Sep;67(9):671-8. doi: 10.1007/BF02762182.
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Enteric duplications. Thirty-seven cases: a vascular theory of pathogenesis.肠道重复畸形。37例：发病机制的血管学说
Am J Dis Child. 1971 Dec;122(6):501-6.
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Ileal atresia with intestinal duplication.回肠闭锁合并肠道重复畸形。
Indian Pediatr. 1992 Dec;29(12):1573-4.
7
Operative mangement of intestinal atresia and stenosis based on pathologic findings.基于病理结果的肠闭锁和狭窄的手术管理。
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