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嗜酸性粒细胞性食管炎中的动力障碍

Dysmotility in Eosinophilic Esophagitis.

作者信息

Chai Charmaine, Krishnan Usha

机构信息

Department of Pediatric Gastroenterology, The Children's Hospital at Westmead, Sydney, NSW, Australia.

Department of Pediatric Gastroenterology, Sydney Children's Hospital, Randwick, Sydney, NSW, Australia.

出版信息

Front Pediatr. 2022 Feb 28;10:853754. doi: 10.3389/fped.2022.853754. eCollection 2022.

Abstract

Eosinophilic esophagitis (EoE) is an immune mediated chronic inflammatory disease resulting from antigen exposure and is characterized by mucosal inflammation with eosinophils. Diagnosis is based on the histological finding of at least 15 eosinophils per high power field in esophageal biopsy specimens from upper gastrointestinal endoscopies. These endoscopies are usually performed in the setting of esophageal dysfunction, however, EoE can occasionally be incidentally diagnosed during endoscopies performed for other indications like coeliac disease. The eosinophilia is in the absence of other causes of esophageal eosinophilia (e.g., parasitic infection, esophageal leiomyomatosis or Crohn's disease). Presentation can be wide ranging and often varies according to age. Infants and younger children can present with choking/gagging, feed refusal, failure to thrive, irritability and vomiting. Older children and adults commonly present with dysphagia, chest pain or food bolus obstruction. EoE was first described in the 1970s, but was only recognized as a distinct disease entity in the 1990s. It has been rising in incidence and prevalence, with reported prevalence ranging between 1 in 2,500 and 1 in 10,000. Although the diagnosis of EoE is dependent on clear histopathologic diagnostic criteria, there is a disconnect between the degree of esophageal eosinophilia and symptom severity especially that of reported dysphagia. Multiple anatomical changes can be seen in the spectrum of presentations of EoE which explain dysphagia, including isolated strictures, diffuse trachealisation, fixed rings, including Schatzki, as well as tissue remodeling and fibrotic changes. However, a majority of EoE patients do not have any of these findings and will still often report ongoing dysphagia. Some will report ongoing dysphagia despite histological remission. This suggests an underlying esophageal dysmotilty which cannot be assessed with endoscopy or correlated with histological changes seen in biopsies. This review will describe the types of motor disturbances seen and their prevalence, the pathophysiological basis of dysmotility seen in EoE, how best to investigate esophageal dysfunction in EoE and the role of manometry in the management of EoE.

摘要

嗜酸性粒细胞性食管炎(EoE)是一种由抗原暴露引起的免疫介导的慢性炎症性疾病,其特征为伴有嗜酸性粒细胞的黏膜炎症。诊断基于上消化道内镜检查食管活检标本中每高倍视野至少15个嗜酸性粒细胞的组织学发现。这些内镜检查通常在食管功能障碍的情况下进行,然而,EoE偶尔也会在因其他适应证(如乳糜泻)进行的内镜检查中被偶然诊断出来。嗜酸性粒细胞增多症不存在其他导致食管嗜酸性粒细胞增多的原因(如寄生虫感染、食管平滑肌瘤病或克罗恩病)。其临床表现广泛,且常因年龄而异。婴儿和年幼儿童可能出现呛噎/作呕、拒食、生长发育迟缓、易怒和呕吐。年龄较大的儿童和成人通常表现为吞咽困难、胸痛或食物团块梗阻。EoE最早于20世纪70年代被描述,但直到20世纪90年代才被确认为一种独特的疾病实体。其发病率和患病率一直在上升,报告的患病率在2500分之一至10000分之一之间。虽然EoE的诊断依赖于明确的组织病理学诊断标准,但食管嗜酸性粒细胞增多的程度与症状严重程度之间存在脱节,尤其是报告的吞咽困难症状。在EoE的各种表现中可以看到多种解剖学变化,这些变化解释了吞咽困难,包括孤立性狭窄、弥漫性气管化、固定环(包括沙茨基环)以及组织重塑和纤维化改变。然而,大多数EoE患者没有这些发现中的任何一项,但仍经常报告持续的吞咽困难。有些人尽管组织学缓解但仍报告持续的吞咽困难。这表明存在潜在的食管运动功能障碍,而这种障碍无法通过内镜检查评估,也与活检中看到的组织学变化无关。本综述将描述所观察到的运动障碍类型及其患病率、EoE中所见运动功能障碍的病理生理基础、如何最好地研究EoE中的食管功能障碍以及食管测压在EoE管理中的作用。

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