Arredondo Montero Javier, Sáez Álvarez Samuel, Herreras Martínez Andrea, Fernández-García Ana, Iglesias Blázquez Cristina
Pediatric Surgery Department, Complejo Asistencial Universitario de León, 24008 León, Castilla y León, Spain.
Pathology Department, Complejo Asistencial Universitario de León, 24008 León, Castilla y León, Spain.
Children (Basel). 2025 Jun 10;12(6):752. doi: 10.3390/children12060752.
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. 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. 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 , with 75% of patients with moderate-to-severe IP inflammation also exhibiting gastric -associated gastritis. All patients except one received proton pump inhibitors, and symptoms improved in all cases. 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 . Further studies are needed to define the clinical significance of pediatric IP and optimal management.
入口斑块(IP)是一种先天性异常,其特征为颈段食管存在胃异位组织。虽然在成人中有广泛描述,但在儿科人群中其特征仍不明确。这项回顾性单中心研究纳入了2018年至2025年间所有诊断为IP的儿科患者(0至14岁)。收集了社会人口统计学和临床数据。一名盲法病理学家评估了IP内炎症的存在及严重程度。纳入了9名患者(中位年龄12岁;范围6至14岁),其中78%为男性。67%的患者出现颈段食管症状,主要为吞咽困难和与胃食管反流病相关的主诉,尽管常伴有嗜酸性食管炎等合并症。3名患者有可能归因于IP的症状(33%)。内镜检查在所有患者中均发现了特征性的边界清晰的鲑鱼红色斑块,3例观察到多个病变。组织学证实所有病例均存在胃异位组织并伴有不同程度的慢性炎症。观察到胃内胃炎的严重程度、IP内炎症的严重程度与[此处原文缺失部分内容]之间存在潜在关联,75%中度至重度IP炎症患者也表现出与胃[此处原文缺失部分内容]相关的胃炎。除1名患者外,所有患者均接受了质子泵抑制剂治疗,所有病例症状均有改善。在我们中心,对颈段食管进行全面且有针对性的检查显著提高了IP的检出率,大多数病例(89%)在过去12个月内被诊断出来。虽然IP大多无症状且为偶然发现,但也可能有症状。在本病例系列中,我们发现IP内炎症的严重程度、胃炎的严重程度与[此处原文缺失部分内容]之间可能存在关联。需要进一步研究来确定儿科IP的临床意义及最佳管理方法。