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Mediastinal foregut duplication cyst presenting as acute respiratory distress in a three-month-old infant: A case report.
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Introduction: Foregut duplication cysts are rare mediastinal malformations that can cause life-threatening respiratory compromise in early infancy and are often misdiagnosed on initial imaging.
Presentation Of Case: A three-month-old boy, born at 37 weeks, developed progressive respiratory distress and cyanosis unresponsive to pneumonia therapy. Chest radiography suggested a hiatal hernia, whereas thoracic ultrasound showed a multiloculated cyst.
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Duplication cysts are congenital anomalies that arise during early embryonic development. They occur in the small intestine, oesophagus, stomach, and colon. Oesophageal duplication cyst (ODC) is rare among newborns, but even rarer in adults.
View Article and Find Full Text PDFIntrapancreatic Gastric Duplication Cysts: A Report of Two Cases and a Systematic Review.
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Department of Pediatric Surgery, Medical University of Warsaw, Warsaw, POL.
Duplications of the gastrointestinal tract are congenital anomalies characterized by a heterogeneous clinical presentation and challenging diagnostic and therapeutic processes. A systematic review was conducted on intrapancreatic gastric duplications in the pediatric population, and we present two clinical cases of patients with this condition. Intrapancreatic gastric duplication is an extremely rare congenital anomaly with variable clinical manifestations and complex management.
View Article and Find Full Text PDFForegut Duplication Cysts in a Patient With Congenital Diaphragmatic Hernia: A Case Report.
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Esophageal duplication cysts are a rare form of foregut developmental abnormality with heterogeneous manifestations due to their variable location and size. Congenital diaphragmatic hernia is a congenital defect resulting from incomplete diaphragm formation, with a wide spectrum of severity. It is typically diagnosed antenatally and managed surgically in the neonatal period.
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