Delayed presentation of congenital diaphragmatic hernia
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Published on: February 5, 2021
Essam A Elhalaby1, Magda H Abo Sikeena
1Department of Pediatric Surgery, Faculty of Medicine, Tanta University, Egypt. eelhalaby@hotmail.com
Insights
Late-presenting congenital diaphragmatic hernia (CDH) poses diagnostic challenges. Early diagnosis and GI contrast studies are crucial for managing these complex pediatric cases.
Area of Science:
- Pediatric Surgery
- Thoracic Surgery
- Medical Diagnostics
Background:
- Late-presenting congenital diaphragmatic hernia (CDH) is difficult to diagnose.
- Delayed presentation can lead to misdiagnosis and treatment delays.
Purpose of the Study:
- To define patterns of delayed CDH presentation.
- To analyze diagnostic and treatment pitfalls in late-presenting CDH.
Main Methods:
- Retrospective review of 15 pediatric CDH patients diagnosed after 2 months.
- Analysis of diagnostic methods including plain radiographs and GI contrast studies.
- Surgical treatment via abdominal approach with primary defect closure.
Main Results:
- Median age at diagnosis was 2.5 years.
- Common presentations included respiratory distress and GI obstruction.
- Plain radiographs were insufficient for diagnosis in most cases; GI contrast studies were essential.
- Misdiagnosis led to inappropriate chest drain insertion in 3 patients.
- All patients survived surgery with symptom improvement.
Conclusions:
- Consider late-presenting CDH in children with persistent GI/respiratory issues and abnormal chest X-rays.
- Nasogastric tube placement is a valuable early diagnostic/therapeutic step.
- GI contrast studies are vital for accurate diagnosis in suspected cases.
Abstract:
The late-presenting congenital diaphragmatic hernia (CDH) represents a considerable diagnostic challenge. This study was undertaken to define various patterns of delayed presentation and to analyze pitfalls in the diagnosis and treatment of these patients. Thirty-three children with CDH were treated between 1993 and 2000; 15 of these (45.5%) who were diagnosed after the age of 2 months-14 years, median of 2.5 years are reported. Thirteen had a Bochdalek hernia and 2 had a Morgagni hernia. The diaphragmatic defect was right-sided in 6 cases and left-sided in 9. Five patients presented acutely, 3 with respiratory distress and 2 with gastrointestinal (GI) obstruction. The remaining 10 presented with chronic respiratory or GI complaints. Inappropriate insertion of a chest drain occurred in 3 patients misdiagnosed as having pleural effusion (2) and a pneumothorax (1). Two patients had previous chest radiographs reported normal. Plain radiographs were sufficient to make a definitive diagnosis in only 6 patients; GI contrast studies were necessary in the other 9. All patients were treated through an abdominal approach with primary closure of the diaphragmatic defect without a patch. A distinct hernia sac was present in 6 cases, and associated malrotation in 6. All except 1 patient survived the operation with rapid improvement of their GI and respiratory symptoms. We conclude that: (1) late-presenting CDH should be included in the differential diagnosis of any child with persistent GI or respiratory problems associated with an abnormal chest X-ray film; (2) nasogastric tube placement must be considered as an early diagnostic or therapeutic intervention when the diagnosis is suspected; and (3) GI contrast studies should be a part of the diagnostic work-up of these patients.
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