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先天性结肠系膜中部疝:新生儿肠梗阻的罕见病因。

Congenital Middle Mesocolic Hernia: A Rare Cause of Neonatal Intestinal Obstruction.

作者信息

Chamely Elias, Antao Brice

机构信息

Department of Paediatric Surgery, Our Lady's Children's Hospital, Crumlin, Dublin 12, Republic of Ireland.

出版信息

J Neonatal Surg. 2016 Oct 10;5(4):58. doi: 10.21699/jns.v5i4.371. eCollection 2016 Oct-Dec.

Abstract

Congenital mesocolic hernia is an extremely rare, but serious cause of intestinal obstruction in children. Given the rarity of this condition, delays in diagnosis and management can have catastrophic consequences. Congenital mesocolic hernias are usually caused by an abnormal rotation of primitive mid-gut and are divided into left and right congenital mesocolic hernias. We report and discuss the clinical and radiological features and management of a neonate with an extremely rare variant, congenital middle mesocolic hernia along with a literature review of this rare condition.

摘要

先天性结肠系膜疝是一种极其罕见但严重的儿童肠梗阻病因。鉴于这种疾病的罕见性,诊断和治疗的延迟可能会带来灾难性后果。先天性结肠系膜疝通常由原始中肠异常旋转引起,分为左、右先天性结肠系膜疝。我们报告并讨论了一名患有极其罕见的先天性中结肠系膜疝新生儿的临床和放射学特征及治疗方法,并对这种罕见疾病进行了文献综述。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f577/5117281/b83cfee10010/jns-5-58.f1.jpg

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