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Tension gastrothorax in late-onset congenital diaphragmatic hernia, a rare but life-threatening condition: A case report

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Abstract
Rationale: Tension gastrothorax is a serious condition that can cause acute respiratory failure, which is mostly related to congenital
diaphragmatic hernia (CDH) in pediatric cases. It is uncommon in late-onset CDH patients, and is difficult to diagnose due to atypical
presentation. It is often misdiagnosed as tension pneumothorax or pleural effusion, leading to delayed treatment and potentially fatal
outcome. In this study, we are reporting our experience of diagnosis and treatment of tension gastrothorax in a late-onset CDH
patient.
Patient concerns: A 2-year old boy presented to this hospital with severe dyspnea and abdominal pain that suddenly occurred
while taking a bath.
Diagnosis: Based on radiological findings we diagnosed tension gastrothorax.
Interventions: Hernia reduction and diaphragmatic defect repair were performed under thoracotomy.
Outcomes: After the operation, the patient’s clinical symptoms and imaging findings improved. At 1-year postoperative follow up,
the patient was well with normal chest x-ray findings.
Lessons: Tension gastrothorax in late-onset CDH is a life-threatening condition that requires rapid diagnosis and treatment. When
the diagnosis is unclear by chest x-ray, chest computed tomography should be performed to confirm the diagnosis. A nasogastric
tube should be inserted whenever possible for diagnosis and gastric decompression. Although laparotomy is the most preferred
approach, we recommend that surgeons consider taking a thoracotomy approach in unstable patients that cannot undergo gastric
decompression before operation.
All Author(s)
I. H. Song
Issued Date
2021
Type
Article
Keyword
congenital diaphragmatic hernialife-threatening conditiontension gastrothorax
Publisher
Lippincott Williams & Wilkins
ISSN
0025-7974 ; 1536-5964
Citation Title
Medicine
Citation Volume
100
Citation Number
7
Citation Start Page
e24815
Citation End Page
e24815
Language(ISO)
eng
DOI
10.1097/md.0000000000024815
URI
http://schca-ir.schmc.ac.kr/handle/2022.oak/2455
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