{"title":"Synchronous Morgagni and Bochdalek Hernias: A Case Report of a Unique Approach to a Rare Finding","authors":"A. Schlager, Adekemi Egunsola, M. Durham","doi":"10.17795/MINSURGERY-33974","DOIUrl":null,"url":null,"abstract":"Introduction: Multipleunilateralcongenitaldiaphragmatichernias(CDH)areextremelyrare,describedonlyfivetimesinthemed-icalliterature. ConcurrentipsilateralBochdalekandMorgagniherniasarerarerstillwithonlytwocasespreviouslydescribed. Inall reportedcasesof multipleconcurrentdefects,theherniaswererepairedinanopenfashion,eitherviaathoracotomyorlaparotomy with both of the two combined Bochdalek and Morgagni hernias repaired via laparotomy. Case Presentation: In this case report we have a 2-day-old who developed respiratory distress and on CT scan was found to have a congenital diaphragmatic hernia (CDH) or eventration. This patient is ideal for this case report because he meets a lot of the previ-ouslyestablishedcriteriaforminimallyinvasiverepairof congenitaldiaphragmatichernias-minimalrespiratorycompromise,no congenitalheartdefects-andhehassynchronousdefectswhichhaveveryrarelybeenseenbefore. Herewepresentthefirstreported caseof concurrentipsilateralBochdalekandMorgagniherniasrepairedinaone-stageminimallyinvasivefashion,approachingthe Bochdalek hernia thoracoscopically and the Morgagni laparoscopically. The patient had a quick recovery post-operatively and he continues to do well. Conclusions: From this experience, we argue that in the right circumstances a completely minimally invasive approach can be taken for synchronous congenital diaphragmatic hernias.","PeriodicalId":158928,"journal":{"name":"Journal of Minimally Invasive Surgical Sciences","volume":"5 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2016-06-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Minimally Invasive Surgical Sciences","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.17795/MINSURGERY-33974","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
Introduction: Multipleunilateralcongenitaldiaphragmatichernias(CDH)areextremelyrare,describedonlyfivetimesinthemed-icalliterature. ConcurrentipsilateralBochdalekandMorgagniherniasarerarerstillwithonlytwocasespreviouslydescribed. Inall reportedcasesof multipleconcurrentdefects,theherniaswererepairedinanopenfashion,eitherviaathoracotomyorlaparotomy with both of the two combined Bochdalek and Morgagni hernias repaired via laparotomy. Case Presentation: In this case report we have a 2-day-old who developed respiratory distress and on CT scan was found to have a congenital diaphragmatic hernia (CDH) or eventration. This patient is ideal for this case report because he meets a lot of the previ-ouslyestablishedcriteriaforminimallyinvasiverepairof congenitaldiaphragmatichernias-minimalrespiratorycompromise,no congenitalheartdefects-andhehassynchronousdefectswhichhaveveryrarelybeenseenbefore. Herewepresentthefirstreported caseof concurrentipsilateralBochdalekandMorgagniherniasrepairedinaone-stageminimallyinvasivefashion,approachingthe Bochdalek hernia thoracoscopically and the Morgagni laparoscopically. The patient had a quick recovery post-operatively and he continues to do well. Conclusions: From this experience, we argue that in the right circumstances a completely minimally invasive approach can be taken for synchronous congenital diaphragmatic hernias.