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First branchial cleft anomalies in children: long-term outcome in 16 patients.

Eur Arch Otorhinolaryngol

January 2025

Otorhinolaryngology, Head and Neck Surgery, University Hospitals Leuven, Leuven, Belgium.

Introduction: First branchial cleft anomalies (FBCA) are rare congenital head and neck malformations, often subject to incorrect diagnosis and treatment. We present our experience with FBCA, focusing on clinical presentation, diagnosis, perioperative relation to the facial nerve, surgical approach, complications and patient satisfaction.

Methods: A consecutive cohort of 16 patients undergoing surgical treatment for FBCA between 1999 and 2021 was analyzed.

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Outcome of Recurrent Tracheoesophageal Fistula Treatment After Esophageal Atresia Repair.

J Pediatr Surg

January 2025

Congenital Oesophageal and Airway Team Utrecht, Departments of Paediatric Surgery and Otorhinolaryngology and Head and Neck Surgery, Wilhelmina Children's Hospital, University Medical Center Utrecht, Utrecht, the Netherlands.

Introduction: Recurrent Tracheoesophageal Fistula (rTEF) is a complication of Esophageal Atresia (EA) that can lead to severe respiratory symptoms. RTEF can be corrected via endotracheal treatment (ET) or surgical treatment (ST). The efficacy of these techniques varies in literature.

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Coronary artery fistulas (CAFs) are rare congenital anomalies, presenting in 0.05-0.9% of cases, characterized by an aberrant connection between a coronary artery and a cardiac chamber or great vessel.

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Objective: To evaluate the clinical efficacy of different surgical methods in congenital preauricular fistula surgery.

Methods: 60 patients with congenital preauricular fistula were selected and randomly divided into a microscope group of 30 cases and a macroscopic group of 30 cases. The microscope team used the fistula separation method to perform surgery along with the fistula opening.

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