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Late-presenting congenital diaphragmatic hernia in children: a clinical spectrum
1Department of Pediatric Surgery, Wroclaw Medical University, M. Sklodowska 52, 50-367 Wroclaw, Poland. baglaj@chdz.am.wroc.pl
Insights
Late-presenting congenital diaphragmatic hernia (CDH) shows varied clinical presentations, with left posterolateral hernias being most common. This review highlights key clinical and surgical aspects of CDH in children.
Area of Science:
- Pediatric Surgery
- Neonatology
- Medical Genetics
Background:
- Late-presenting congenital diaphragmatic hernia (CDH) is a rare condition with diverse clinical manifestations.
- Understanding its spectrum is crucial for timely diagnosis and management.
Purpose of the Study:
- To review articles on late-presenting CDH in children published until 2003.
- To gain insight into the clinical spectrum, and discuss clinical and surgical aspects of this CDH variant.
Main Methods:
- A collective review of 125 articles reporting on 362 pediatric patients with late-presenting CDH.
- Analysis of anatomical types, presentation age, symptoms, associated anomalies, and outcomes.
Main Results:
- Left posterolateral hernia was dominant (79.4%). Male-to-female ratio was 2:1.
- Right CDH often presented within the 1st year (65%) with chronic symptoms (57.4%), while left CDH had acute presentation (60.5%).
- Preoperative mortality was 3.9%, with 12.4% experiencing complications. Postoperative mortality was 2.2%.
Conclusions:
- Late-presenting CDH presents with a wide clinical spectrum influenced by herniation timing and displaced viscera.
- Findings support a congenital defect with acquired herniation, emphasizing the need for individualized management strategies.
Abstract:
Articles dealing with late-presenting congenital diaphragmatic hernia (CDH) in children published until 2003 were collectively reviewed. The main purpose of the presented study was to gain insight into the clinical spectrum of this variant of CDH and to discuss its clinical and surgical aspects. In 125 articles, 362 patients were reported. Left posterolateral hernia was the dominant anatomical type, found in 79.4% of the children. Male-to-female distribution was nearly 2:1 in both right- and left-sided CDH. Associated anomalies were noted in 8.6% of children. Sixty-five percent of children with right CDH presented within the 1st year of life, whereas only 41.7% of patients with left CDH belonged to this age group. The children with right CDH presented with chronic symptoms in 57.4% of cases, while among those with left CDH, acute presentation prevailed, constituting 60.5% of this group. No strict correlation between age and clinical symptoms was noted, although the youngest patients tended to present with respiratory symptoms. Late-presenting diaphragmatic hernia is associated with a wide range of clinical symptoms occurring in various constellations. Dyspnea and vomiting were the most frequent symptoms found in patients with either chronic or acute manifestation. Preoperative mortality was 3.9% (14 children). In 45 children (12.4%), complications resulting from diaphragmatic hernia were noted, and in a further 11 children iatrogenic preoperative complications were noted. Among 152 children with reported CDH, true hernia with sac was found in 32.7%. Eight children (2.2%) died in the early postoperative period, while a further 13 patients (3.6%) had postoperative complications requiring surgical management. Recurrence of hernia was noted in seven children (1.9%). This collective review of basic epidemiological and clinical data from a large group of patients seems to support a hypothesis for a congenital nature of the diaphragmatic defect and an acquired nature of "herniation" of the viscera. The wide clinical spectrum of late-presenting CDH seems to be conditioned by two factors: timing of herniation and type of intraabdominal viscera displaced into the chest.
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