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一名4个月大婴儿的先天性混合型巨大食管裂孔疝。

Congenital mixed giant hiatal hernia in a four-month-old infant.

作者信息

Jiménez Muñoz M, Benítez Gómez I L

机构信息

Hospital Universitario Virgen del Rocío. Sevilla (Spain).

出版信息

Cir Pediatr. 2020 Jan 20;33(1):47-50.

Abstract

INTRODUCTION

Congenital hiatal hernia is a rare pathology, presenting at 28 months of age on average. Paraesophageal/mixed hernias cause recurrent respiratory infections, vomiting, anemia, and growth failure.

CLINICAL CASE

Four-month-old infant, with irritability since birth and partial feeding intolerance in the last 24 hours. A partial intrathoracic stomach was evidenced in the esophago-gastro-duodenal contrast study. A thoraco-abdominal CT scan was carried out, with giant mixed hiatal hernia, right posterolateral diaphragmatic hernia, and congenital short esophagus being considered as potential diagnoses. A giant mixed hiatal hernia was noted during surgery. Laparoscopic herniorrhaphy and Nissen fundoplication were performed.

DISCUSSION

In the pediatric population, Bochdalek's hernia and Morgagni's hernia are the most frequent congenital diaphragmatic hernias. Hiatal hernia is rare and causes gastrointestinal symptoms more frequently. Surgery is the treatment of choice, with the objective of preventing or minimizing these symptoms as well as gastric volvulus.

摘要

引言

先天性食管裂孔疝是一种罕见的病症,平均发病年龄为28个月。食管旁/混合型疝会导致反复呼吸道感染、呕吐、贫血和生长发育迟缓。

临床病例

一名4个月大的婴儿,自出生以来易激惹,在过去24小时内出现部分喂养不耐受。食管-胃-十二指肠造影检查证实胸腔内有部分胃。进行了胸腹CT扫描,潜在诊断考虑为巨大混合型食管裂孔疝、右后外侧膈疝和先天性短食管。手术中发现巨大混合型食管裂孔疝。实施了腹腔镜疝修补术和nissen胃底折叠术。

讨论

在儿科人群中,博赫dalek疝和莫尔加尼疝是最常见的先天性膈疝。食管裂孔疝罕见,更常引起胃肠道症状。手术是首选治疗方法,目的是预防或减轻这些症状以及胃扭转。

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