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Esophageal Atresia and Intrathoracic Stomach in a Complex Case of Congenital Anomalies

Bibliographic Data

ID15715005
AuthorsPhilipp Christoph Köhler (Olgahospital, corresponding author), Raphael Staubach (0000-0002-3293-2879, Olgahospital), Helen Glosse (Olgahospital), Loredana Delle Chiaie (0000-0002-4457-0297, Klinikum Stuttgart), Ventsislav Sheytanov (Klinik für Herzchirurgie Karlsruhe), Steffan Loff (0000-0003-4788-3181, Klinikum Stuttgart)
Year2025
Volume12
Issue9
Pages1244-1244
Publication date2025-09-16
Open AccessYes
TypeARTICLE
VenueChildren (JOURNAL)
Journal identifiersISSN: 2227-9067 • E-ISSN: 2227-9067
PublisherMultidisciplinary Digital Publishing Institute (PUBLISHER • CH)
DOI10.3390/children12091244
PMID41007109
OpenAlexW4414297774
LanguageEN
References cited12

Background/Objectives: Complex cases in pediatric surgery involving multiple congenital anomalies pose significant diagnostic and therapeutic challenges. These conditions require coordinated interdisciplinary care tailored to the individual patient. We present a case of syndromic congenital anomalies in a neonate, later diagnosed with CHARGE syndrome, to illustrate the importance of staged, multidisciplinary management. Methods: A 34-year-old woman in her third pregnancy developed significant polyhydramnios at 31 weeks of gestation, followed by preterm labor. The neonate presented with esophageal atresia with tracheoesophageal fistula (EA/TEF), intrathoracic stomach, aortic coarctation, patent ductus arteriosus, atrial septal defect, and bilateral choanal atresia. A structured treatment protocol was developed and implemented at Klinikum Stuttgart by an interdisciplinary team comprising gynecology, pediatric surgery, cardiology, ENT, neonatology, and genetics. Results: Initial pediatric surgical procedures included ligation of the tracheoesophageal fistula, repositioning of the intrathoracic stomach, and primary esophageal anastomosis. Cardiovascular anomalies were managed through staged interventions. Bilateral choanal atresia was surgically corrected. Genetic testing confirmed CHARGE syndrome. Postoperative care included respiratory support, enteral nutrition, and regular esophageal dilations. Due to persistent reflux esophagitis, antireflux surgery is planned. Conclusions: This case underscores the importance of a highly individualized and interdisciplinary approach in the management of syndromic congenital anomalies. The presence of CHARGE syndrome with multiple system involvement required careful staging of surgical interventions and long-term coordination of follow-up care. Early genetic diagnosis and integrated team planning were critical in optimizing outcomes in this complex neonatal case

Atresia · CHARGE syndrome · Choanal atresia · Esophagus · Pediatric Surgeon · Pediatric surgery · Polyhydramnios · Tracheoesophageal fistula · Congenital Ear and Nasal Anomalies · Esophageal and GI Pathology · Tracheal and airway disorders

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