Published online Nov 26, 2022. doi: 10.12998/wjcc.v10.i33.12313
Peer-review started: June 21, 2022
First decision: August 1, 2022
Revised: August 24, 2022
Accepted: October 17, 2022
Article in press: October 17, 2022
Published online: November 26, 2022
Processing time: 155 Days and 6.5 Hours
Congenital esophageal stenosis (CES) is a rare malformation of the digestive tract. Endoscopic dilation and thoracotomy have been the main treatments for CES. However, there is no well-defined management protocol. Magnetic compression stricturoplasty (MCS) has been used in refractory esophageal stricture in children after esophageal atresia.
We describe the first case of MCS for CES in one female child patient. The child (aged 3 years and 1 mo) was admitted due to frequent vomiting and choking after eating complementary food since 7 mo old. Esophagography and gastroendoscopy showed that there was stenosis in the lower esophagus, suggesting a diagnosis of CES. The patient did not receive any treatment for esophageal stricture including surgery or endoscopic dilation procedures before MCS. MCS procedure was smoothly conducted without complications. At 24 mo after MCS, durable esophageal patency without dysphagia was achieved.
MCS may serve as an alternative and efficient method for patients with CES.
Core Tip: Magnetic compression stricturoplasty (MCS) is a relatively safe dredge method for patients with postoperative obstruction, stricture, or dehiscence of anastomosis. For the first time, we describe the application of MCS in treating congenital esophageal stenosis (CES) without using endoscopic bougienage and dilation treatment in a child patient. The data on diagnosis, treatment, and long-term follow-up of CES are analyzed. Additionally, key properties of MCS in treating segmental fibromuscular hypertrophy stricture following CES are discussed.