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Published in: Pediatric Surgery International 7/2017

01-07-2017 | Original Article

Pediatric Morgagni diaphragmatic hernia: a descriptive study

Authors: Jamie Golden, Wesley E. Barry, Gene Jang, Nam Nguyen, David Bliss

Published in: Pediatric Surgery International | Issue 7/2017

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Abstract

Introduction

The Morgagni hernia (MH) accounts for 3–4% of congenital diaphragmatic hernias. There is a paucity of data regarding this rare defect. The purpose of this study is to describe the characteristics of children with MH, surgical approaches for repair, and patient outcomes.

Methods

Pediatric patients (ages 0–18) with a MH from 2002 to 2014 at a single, freestanding pediatric hospital were retrospectively reviewed. Patient presentation, demographics, operative methods and findings, and outcomes were evaluated.

Results

Twenty-six infants and children with a congenital MH were treated. There were 20 males (77%) and six females (23%) with a median age at diagnosis of 14.75 months (range 1 week to 13 years). Half were symptomatic. Sixteen hernias were repaired laparoscopically, nine by an open approach, and one laparoscopic converted to open. Colon was the most commonly herniated organ (N = 14). Hernia sacs were found in 22 patients of which, 20 were resected. Two patients underwent treatment with ECLS. There was one mortality in a patient who underwent repair on ECLS in the setting of an omphalocele and SVC obstruction. There were no recurrences in our sample.

Conclusion

In this series, congenital MH appears to have a male predominance, frequently presents with pulmonary symptoms, and has excellent outcomes regardless of operative approach.
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Metadata
Title
Pediatric Morgagni diaphragmatic hernia: a descriptive study
Authors
Jamie Golden
Wesley E. Barry
Gene Jang
Nam Nguyen
David Bliss
Publication date
01-07-2017
Publisher
Springer Berlin Heidelberg
Published in
Pediatric Surgery International / Issue 7/2017
Print ISSN: 0179-0358
Electronic ISSN: 1437-9813
DOI
https://doi.org/10.1007/s00383-017-4078-3

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