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Pulmonary sequestration cyst in a patient of cerebral palsy
Bilal Mirza1, Muhammad Saleem, Lubna Ijaz
1Department of Pediatric Surgery, The Children's Hospital and The Institute of Child Health, Lahore, Pakistan.
Insights
Pulmonary sequestration cysts are rare in children, often found incidentally. This case highlights a complex pediatric presentation involving multiple congenital anomalies, including a pulmonary sequestration cyst.
Area of Science:
- Pediatric Surgery
- Thoracic Surgery
- Congenital Anomalies
Background:
- Pulmonary sequestration cysts are uncommon in pediatric patients, frequently discovered as incidental findings.
- These cysts are often associated with other congenital abnormalities, notably congenital diaphragmatic hernia.
Purpose of the Study:
- To report a rare case of pediatric pulmonary sequestration cyst.
- To discuss the diagnostic and management challenges in a patient with multiple congenital anomalies.
Main Methods:
- Case report of a pediatric patient with cerebral palsy presenting with vomiting and recurrent chest infections.
- Diagnosis of hiatal hernia via computed tomography scan of the chest.
- Surgical exploration revealing pulmonary sequestration cyst, hiatal hernia, malrotation, and Meckel's diverticulum.
Main Results:
- A pediatric patient with cerebral palsy presented with symptoms suggestive of gastrointestinal and respiratory issues.
- Computed tomography identified a hiatal hernia.
- Surgical intervention revealed a complex case with a pulmonary sequestration cyst and other congenital anomalies.
Conclusions:
- Pulmonary sequestration cysts can present atypically in children with co-existing congenital anomalies.
- Multifocal congenital anomalies require comprehensive surgical planning and execution.
- Transhiatal approach was utilized for the management of the sequestration cyst in this complex case.
Abstract:
Pulmonary sequestration cyst is a rare entity in pediatric patients. Most of the time, it is diagnosed as an incidental finding. It is associated with other congenital anomalies, especially congenital diaphragmatic hernia. We report a patient of cerebral palsy presented with vomiting and recurrent chest infections. He was diagnosed to have hiatal hernia on computed tomography scan of chest. At operation, a pulmonary sequestration cyst along with hiatal hernia, malrotation, and meckel's diverticulum was encountered. The sequestration cyst was managed through transhiatal approach.
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