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"Bronchogenic"

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"Bronchogenic"

Case Reports

[English]
Intrapulmonary Bronchogenic Cyst in an Infant: Rare Presentation and Insights From Literature
Ramyasree Bade, Shailesh Solanki, Shivani Dogra, Nitin James Peters, Jai Kumar Mahajan
Adv Pediatr Surg 2025;31(2):87-92.   Published online December 24, 2025
DOI: https://doi.org/10.13029/aps.2025.31.2.87
Intrapulmonary bronchogenic cysts are rare congenital anomalies that often present diagnostic and management challenges due to nonspecific symptoms. We report a one-year-old female with progressive respiratory distress who was initially misdiagnosed with pneumothorax. Imaging revealed a large intrapulmonary cyst, and surgical excision confirmed the diagnosis. Early intervention ensured a favorable outcome, with no recurrence in one year. This case highlights the importance of considering bronchogenic cysts in pediatric respiratory distress and emphasizes the value of timely surgical management.
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[English]
Esophageal Atresia with Bronchogenic Cyst
Youngmin Kim, Chaeyoun Oh, Joong-Kee Youn, Ji-Won Han, Hyun-Young Kim, Sung-Eun Jung
J Korean Assoc Pediatr Surg 2017;23(1):5-8.   Published online June 26, 2017
DOI: https://doi.org/10.13029/jkaps.2017.23.1.5

A baby was diagnosed with esophageal atresia (EA) with tracheoesophageal fistula (TEF) on the next day after birth, and end-to-end anastomosis of esophagus with TEF ligation was performed. The distance between proximal and distal esophageal pouch was checked as 3 vertebral body lengths and a 1 cm-sized bronchogenic cyst (BC) was identified near carina on the right side, just below the proximal esophageal pouch. This case report described the baby who have a BC was located between the both esophageal pouch and a longer esophageal gap than usual EA with distal TEF.

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[English]
Mediastinal Bronchogenic Cyst Misdiagnosed as Asthma and Dysphagia in a Child: One Case Report
Seock Yeol Lee, Cheol Woo Jeon, Seung Jin Lee, Cheol Sae Lee, Kihl Rho Lee
J Korean Assoc Pediatr Surg 2008;14(1):94-97.   Published online June 30, 2008
DOI: https://doi.org/10.13029/jkaps.2008.14.1.94

A 19-month-old boy suffered from stridor and dysphagia. He was taking asthma medication for a few months, but symptoms did not improve. After admission, a chest CT showed a posterior mediastinal mass, which compressed the trachea and esophagus. The removed mass via open thoracotomy was a bronchogenic cyst on histopathology. Postoperatively, stridor and dysphagia disappeared. In case of persistent and refractory stridor or dysphagia in children, congenital lesions including bronchogenic cyst need to be ruled out.

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