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Herniation through the foramen of Morgagni: early diagnosis and treatment
Ahmed H Al-Salem1, Akhter Nawaz, Hilal Matta
1Depatment of Surgery, Qatif Central Hospital, Saudi Arabia.
Insights
Congenital Morgagni hernias (MH) are rare, often presenting with recurrent chest infections beyond the neonatal period. Early diagnosis and surgical intervention are crucial for managing this condition and reducing associated morbidity.
Area of Science:
- Pediatric Surgery
- Thoracic Surgery
- Congenital Abnormalities
Background:
- Congenital diaphragmatic hernias (CDH) are common, with most occurring via the foramen of Bochdalek.
- Herniation through the foramen of Morgagni (MH) is a rare subtype of CDH.
Purpose of the Study:
- To analyze the clinical presentation, diagnosis, and management of congenital Morgagni hernias (MH) in children.
- To highlight the frequency and associated morbidities of MH in a pediatric population.
Main Methods:
- Retrospective review of 15 children diagnosed with congenital MH over 15 years.
- Analysis of clinical data including presentation, diagnostic methods (radiography, barium enema, CT), surgical approach, and associated anomalies.
Main Results:
- MH represented 11% of all CDH cases, with a male predominance.
- Most patients (80%) presented with recurrent chest infections; neonatal presentation with acute respiratory distress (ARD) was rare.
- Associated anomalies were common, including malrotation (26.7%), congenital heart disease (26.7%), and Down's syndrome (20%).
- Transabdominal surgery was the primary approach, with all cases having a hernia sac.
Conclusions:
- Congenital MH is relatively frequent in this cohort and rarely presents neonatally.
- Late-presenting MH causes significant morbidity, primarily through recurrent chest infections.
- Clinical awareness, prompt diagnosis, and surgical treatment are essential for optimal outcomes in pediatric MH.
Abstract:
The majority of congenital diaphragmatic hernias (CDH) occur through the foramen of Bochdalek; herniation through the foramen of Morgagni (MH) is rare. Fifteen children (12 males and 3 females) with congenital MH (7 right, 3 left, 5 bilateral) were treated over a period of 15 years, comprising 11% of a total of 135 children with different types of CDH. The majority (12, 80%) had repeated chest infections. In 1 the hernia was discovered accidentally during evaluation of trauma, and another presented in the neonatal period with acute respiratory distress (ARD). The diagnosis was made on plain lateral chest radiograph when there was anterior herniation of bowel loops, and in these cases the diagnosis was confirmed by barium enema. Computed tomography was useful in preoperative diagnosis when the hernia contents were solid. All patients were operated upon transabdominally except 1, and in all cases there was a hernia sac. Associated anomalies were present in 10 (66.7%) patients: 4 (26.7%) had malrotation, 4 (26.7%) congenital heart disease, and 3 (20%) Down's syndrome. Our study shows a relatively high frequency of MH in our patients. MH rarely presents in the neonatal period, but when it does, it causes ARD. The majority of patients with MH present beyond the neonatal period with repeated attacks of chest infection, and although late-presenting MH is relatively benign, it nevertheless causes significant morbidity. Thus, clinical awareness and early diagnosis and surgical treatment are important factors.
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