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Published on: February 5, 2021
Typical and atypical presentations of congenital diaphragmatic hernia - a report of 2 cases
1Department of Radiology, LAUTECH College of Health Sciences, PMB 4400, Osogbo, Osun state, Nigeria.
Insights
Congenital diaphragmatic hernias (CDH) are rare defects. Early diagnosis via chest radiography is crucial for timely intervention and reducing mortality in resource-poor settings.
Area of Science:
- Pediatric Surgery
- Diagnostic Imaging
- Embryology
Background:
- Congenital diaphragmatic hernia (CDH) arises from embryologic defects in diaphragm formation.
- CDH is a rare but potentially fatal condition in neonates and infants.
- Timely diagnosis and management are critical for improving patient outcomes.
Observation:
- Two cases of CDH are presented: one with late presentation (11-month-old) and one with early, typical presentation (1-day-old).
- Both diagnoses were established using chest radiographs.
- The study highlights the diagnostic utility of radiography in identifying CDH.
Findings:
- Radiologists play a pivotal role in the early detection of CDH, even in resource-limited environments.
- Chest radiography is an effective tool for diagnosing congenital diaphragmatic hernias.
- Prompt radiographic diagnosis facilitates essential early intervention.
Implications:
- Early diagnosis of CDH through radiography is vital for reducing mortality rates.
- Effective management strategies can be implemented promptly following early diagnosis.
- This emphasizes the importance of radiological expertise in managing rare congenital defects in diverse healthcare settings.
Abstract:
Congenital diaphragmatic hernias occur through embryologic defects in the diaphragm. We present 2 cases of congenital diaphragmatic hernia, the first case was a late presentation in an 11 month old child, and the second case was an early typical presentation in a day old child, both diagnoses were made on chest radiographs. The paper is focused on the key role of the radiologist in a resource poor environment to make early diagnosis of this fatal and rare condition. Early diagnosis of this defect is essential. This will allow timely intervention and appropriate management, therefore, reducing the mortality associated with the condition.
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