Surgical management of congenital lobar emphysema: A 15 years experience in a tertiary thoracic surgery unit

Essam Elbadry Hashim Mohamed , Ayman Mohamed Mohamed Abdel Ghaffar , Khaled Mohamed Abdel-Aal , Abdelhady Ahmed Helmy , Mostafa Ashry
{"title":"Surgical management of congenital lobar emphysema: A 15 years experience in a tertiary thoracic surgery unit","authors":"Essam Elbadry Hashim Mohamed ,&nbsp;Ayman Mohamed Mohamed Abdel Ghaffar ,&nbsp;Khaled Mohamed Abdel-Aal ,&nbsp;Abdelhady Ahmed Helmy ,&nbsp;Mostafa Ashry","doi":"10.1016/j.jescts.2018.10.001","DOIUrl":null,"url":null,"abstract":"<div><h3>Background</h3><p>congenital lobar emphysema is a rare cause of respiratory distress in neonates and infants. It was treated by lobectomy since 1943.</p><p>The aim of this study was to present our experience in the diagnosis and surgical treatment of congenital lobar emphysema cases and highlight the effect of multi-displinary team work on the outcome.</p></div><div><h3>Methods</h3><p>We retrospectively analyzed data of patients operated for congenital lobar emphysema at cardiothoracic surgery department, Sohag university hospital over the period of 15 years starting from January 2000 and ending in December 2015.</p></div><div><h3>Results</h3><p>Total number of cases was fifty three. Males were 39 (74%) while females were 14 (26%). Mean age was 12 weeks (3 weeks - 15 months). Six patients (11%) had associated cardiac anomalies. Main clinical presentations were acute respiratory distress and recurrent chest infection. Left upper lobe was affected in 35 cases (66%), right upper lobe in 10 cases (19%) and right middle lobe in 8 cases (15%). All cases were subjected to anatomical lobectomy by thoracotomy. One patient was subjected to patent ductus arteriosus ligation simultaneously with left upper lobectomy at the same operative setting. Post operative complications were reported in 8 cases (15%) and one patient of them died from sepsis and respiratory failure (1.9%). Postoperatively, all surviving patients were followed up for one year in the outpatient clinic.</p></div><div><h3>Conclusions</h3><p>congenital lobar emphysema is a life threatening disease. Early diagnosis and surgical management by a multi-displinary team is the golden key for favorable and safe outcome.</p></div>","PeriodicalId":100843,"journal":{"name":"Journal of the Egyptian Society of Cardio-Thoracic Surgery","volume":"26 4","pages":"Pages 308-317"},"PeriodicalIF":0.0000,"publicationDate":"2018-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/j.jescts.2018.10.001","citationCount":"3","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of the Egyptian Society of Cardio-Thoracic Surgery","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1110578X18300634","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 3

Abstract

Background

congenital lobar emphysema is a rare cause of respiratory distress in neonates and infants. It was treated by lobectomy since 1943.

The aim of this study was to present our experience in the diagnosis and surgical treatment of congenital lobar emphysema cases and highlight the effect of multi-displinary team work on the outcome.

Methods

We retrospectively analyzed data of patients operated for congenital lobar emphysema at cardiothoracic surgery department, Sohag university hospital over the period of 15 years starting from January 2000 and ending in December 2015.

Results

Total number of cases was fifty three. Males were 39 (74%) while females were 14 (26%). Mean age was 12 weeks (3 weeks - 15 months). Six patients (11%) had associated cardiac anomalies. Main clinical presentations were acute respiratory distress and recurrent chest infection. Left upper lobe was affected in 35 cases (66%), right upper lobe in 10 cases (19%) and right middle lobe in 8 cases (15%). All cases were subjected to anatomical lobectomy by thoracotomy. One patient was subjected to patent ductus arteriosus ligation simultaneously with left upper lobectomy at the same operative setting. Post operative complications were reported in 8 cases (15%) and one patient of them died from sepsis and respiratory failure (1.9%). Postoperatively, all surviving patients were followed up for one year in the outpatient clinic.

Conclusions

congenital lobar emphysema is a life threatening disease. Early diagnosis and surgical management by a multi-displinary team is the golden key for favorable and safe outcome.

先天性大叶性肺气肿的外科治疗:三级胸外科15年的经验
背景:先天性大叶性肺气肿是新生儿和婴儿呼吸窘迫的罕见病因。自1943年以来一直采用肺叶切除术治疗。本研究的目的是介绍我们在先天性肺气肿病例的诊断和手术治疗方面的经验,并强调多学科团队合作对结果的影响。方法回顾性分析2000年1月至2015年12月15年间苏哈格大学附属医院心胸外科先天性肺气肿患者的手术资料。结果共53例。男性39人(74%),女性14人(26%)。平均年龄12周(3周到15个月)。6例患者(11%)伴有心脏异常。主要临床表现为急性呼吸窘迫和复发性胸部感染。左上叶35例(66%),右上叶10例(19%),右中叶8例(15%)。所有病例均行解剖性开胸肺叶切除术。1例患者在同一手术环境下同时行左上肺叶切除术和动脉导管未闭结扎术。术后并发症8例(15%),其中1例死于败血症和呼吸衰竭(1.9%)。术后所有存活患者在门诊随访1年。结论先天性大叶性肺气肿是一种危及生命的疾病。多学科团队的早期诊断和手术治疗是获得良好和安全结果的金钥匙。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信