Marisa E. Schwab , Karthik Balakrishnan , Stephanie D. Chao
{"title":"Fourth branchial cleft cyst presenting as a mediastinal mass in a neonate: a case report","authors":"Marisa E. Schwab , Karthik Balakrishnan , Stephanie D. Chao","doi":"10.1016/j.epsc.2025.103017","DOIUrl":null,"url":null,"abstract":"<div><h3>Introduction</h3><div>Fourth branchial cleft anomalies are a rare congenital condition with varying presentations. Pediatricians and pediatric subspecialists must be familiar with this entity.</div></div><div><h3>Case presentation</h3><div>A 4-day old term female presented with increased work of breathing. Exam was notable for intermittent subcostal retractions. X-ray showed a mediastinal shadow. Chest CT showed a large mass extending from the neck into the mediastinum. Interventional radiology placed a pigtail into the mass via the left neck. This drained milky cloudy fluid for seven weeks. After transfer to a quaternary children's hospital, an MRI showed a persistent large thick-walled cyst tracking into the neck.</div><div>Laryngoscopy, bronchoscopy and esophagoscopy initially didn't show anomalies. Methylene blue dye was injected into the drain and seen to exit from a left pyriform sinus tract. This was confirmed with on-table fluoroscopy.</div><div>Two days later, she underwent injection of sclerosing agents and contrast via the drain under fluoroscopy. The sinus tract was cauterized and suture ligated using laryngoscopy. Laryngoscopy a few days later revealed no patent sinus tract. Sclerosant was again injected. Ultrasound after one month showed a slightly decreased mediastinal mass. Ultrasound three months later was significantly decreased size. At 7-month follow-up, the patient remains asymptomatic, feeding and growing well.</div></div><div><h3>Conclusion</h3><div>Fourth branchial anomalies are rare but must be considered in a pediatric patient of any age presenting with a neck or mediastinal mass.</div></div>","PeriodicalId":45641,"journal":{"name":"Journal of Pediatric Surgery Case Reports","volume":"117 ","pages":"Article 103017"},"PeriodicalIF":0.2000,"publicationDate":"2025-04-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Pediatric Surgery Case Reports","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2213576625000624","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"PEDIATRICS","Score":null,"Total":0}
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Abstract
Introduction
Fourth branchial cleft anomalies are a rare congenital condition with varying presentations. Pediatricians and pediatric subspecialists must be familiar with this entity.
Case presentation
A 4-day old term female presented with increased work of breathing. Exam was notable for intermittent subcostal retractions. X-ray showed a mediastinal shadow. Chest CT showed a large mass extending from the neck into the mediastinum. Interventional radiology placed a pigtail into the mass via the left neck. This drained milky cloudy fluid for seven weeks. After transfer to a quaternary children's hospital, an MRI showed a persistent large thick-walled cyst tracking into the neck.
Laryngoscopy, bronchoscopy and esophagoscopy initially didn't show anomalies. Methylene blue dye was injected into the drain and seen to exit from a left pyriform sinus tract. This was confirmed with on-table fluoroscopy.
Two days later, she underwent injection of sclerosing agents and contrast via the drain under fluoroscopy. The sinus tract was cauterized and suture ligated using laryngoscopy. Laryngoscopy a few days later revealed no patent sinus tract. Sclerosant was again injected. Ultrasound after one month showed a slightly decreased mediastinal mass. Ultrasound three months later was significantly decreased size. At 7-month follow-up, the patient remains asymptomatic, feeding and growing well.
Conclusion
Fourth branchial anomalies are rare but must be considered in a pediatric patient of any age presenting with a neck or mediastinal mass.