
doi: 10.1007/bf02725668
pmid: 14979396
Foregut duplication cysts are rare congenital anomalies of enteric origin. In majority of the patients, the diagnosis is made in infancy. The authors report 4 cases of mediastinal foregut duplication cyst in children diagnosed on CT/MRI and confirmed on histopathology. In none of the cases the cysts had intraspinal extension nor heterotopic gastric mucosa.
Male, Laparotomy, India, Infant, Prognosis, Magnetic Resonance Imaging, Risk Assessment, Sampling Studies, Intestines, Treatment Outcome, Mediastinal Cyst, Child, Preschool, Humans, Esophageal Cyst, Female, Child, Digestive System Abnormalities
Male, Laparotomy, India, Infant, Prognosis, Magnetic Resonance Imaging, Risk Assessment, Sampling Studies, Intestines, Treatment Outcome, Mediastinal Cyst, Child, Preschool, Humans, Esophageal Cyst, Female, Child, Digestive System Abnormalities
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