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Updated: Jul 19, 2026

Implementation of Non-invasive Point of Care Transient Elastography for Evaluation of Liver Disease in Pediatric Populations with Cystic Fibrosis
Published on: August 29, 2025
[Meconium ileus as a first symptom of cystic fibrosis in a newborn]
R Nekl1, A Mocková, J Bierhanzlová
1Neonatologické oddelení FN, Plzen. robertnekl@seznam.cz
Insights
This case study highlights meconium ileus as an early indicator of cystic fibrosis in newborns. Early diagnosis and surgical intervention, followed by genetic testing, are crucial for managing this condition.
Area of Science:
- Neonatology
- Pediatric Surgery
- Medical Genetics
Background:
- Cystic Fibrosis (CF) is a genetic disorder affecting multiple organs.
- Meconium ileus is a common neonatal complication of CF, presenting as bowel obstruction.
Observation:
- A newborn presented with meconium ileus, the initial clinical manifestation.
- The case underscores the diagnostic challenges and importance of timely intervention.
Findings:
- The study details the diagnostic pathway for neonatal ileus.
- Surgical management was performed, followed by essential follow-up investigations.
- Genetic confirmation of cystic fibrosis was necessary.
Implications:
- Early recognition of meconium ileus is vital for prompt CF diagnosis.
- Comprehensive diagnostic and surgical strategies improve neonatal outcomes.
- Long-term follow-up is critical for managing cystic fibrosis in infants.
Abstract:
The authors present a case of cystic fibrosis in a newborn. The first symptom of cystic fibrosis in this case was meconium ileus. They describe correct diagnostic method of ileus in newborn, consecutive operation and last but not least they show necessity of follow-up investigations to verification of cystic fibrosis.
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