Pediatric Heterotopic Gastric Mucosa of the Cervical Esophagus (Inlet Patch)
Case Series with Clinical, Endoscopic, and Histopathological Correlation
Bibliographic Data
| ID | 15717234 |
|---|---|
| Authors | Javier Arredondo Montero (0000-0002-0943-6367, Complejo Asistencial Universitario de Palencia, corresponding author), Samuel Sáez Álvarez (Complejo Asistencial Universitario de Palencia), Alfredo Martı́nez (0000-0003-4882-4044, Complejo Asistencial Universitario de Palencia), Andrea Herreras Martínez (Complejo Asistencial Universitario de León), Ana Fernández-García (Complejo Asistencial Universitario de Palencia), Cristina Iglesias Blázquez (0000-0002-8844-0048, Complejo Asistencial Universitario de Palencia) |
| Year | 2025 |
| Volume | 12 |
| Issue | 6 |
| Pages | 752-752 |
| Publication date | 2025-06-10 |
| Open Access | Yes |
| Type | ARTICLE |
| Venue | Children (JOURNAL) |
| Journal identifiers | ISSN: 2227-9067 • E-ISSN: 2227-9067 |
| Publisher | Multidisciplinary Digital Publishing Institute (PUBLISHER • CH) |
| DOI | 10.3390/children12060752 |
| PMID | 40564709 |
| OpenAlex | W4411187005 |
| Language | EN |
| References cited | 24 |
Introduction: Inlet patch (IP) is a congenital anomaly characterized by gastric heterotopia in the cervical esophagus. While extensively described in adults, it remains poorl characterized in pediatric populations. Material and Methods: This retrospective, single-center study included all pediatric patients (0-14 years) diagnosed with IP between 2018 and 2025. Sociodemographic and clinical data were collected. A blinded pathologist assessed the presence and severity of inflammation within the IP. Results: Nine patients (median age, 12 years; range, 6-14 years) were included, with 78% beingmale. Cervical esophageal symptoms were identified in 67%, primarily dysphagia and gastroesophageal reflux disease-related complaints, although concomitant conditions such as eosinophilic esophagitis were frequently present. Three patients had symptoms potentially attributable to IP (33%). Endoscopic examination revealed characteristic well-demarcated salmon-red plaques in all patients, with multiple lesions observed in three cases. Histology confirmed gastric heterotopia with varying degrees of chronic inflammation in all cases. A potential association was observed between the severity of gastritis in the stomach, the severity of inflammation in the IP, and the presence of H. pylori , with 75% of patients with moderate-to-severe IP inflammation also exhibiting gastric H. pylori -associated gastritis. All patients except one received proton pump inhibitors, and symptoms improved in all cases. Conclusions: A thorough and targeted examination of the cervical esophagus significantly increased IP detection at our center, with most cases (89%) being diagnosed in the last 12 months. While mostly asymptomatic and incidental, IP can be symptomatic. In this case, series, we found a possible association between the severity of inflammation in the IP, the severity of gastritis, and the presence of H. pylori . Further studies are needed to define the clinical significance of pediatric IP and optimal management
Biology · Choristoma · Esophagus · Gastric mucosa · Pathology · Series (stratigraphy · Stomach · Eosinophilic Esophagitis · Gastrointestinal disorders and treatments · Gastrointestinal Tumor Research and Treatment · Medicine · Gastroenterology · Internal Medicine
| Highly cited | No |
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