Eosinophilic Esophagitis

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Key points

  • Over the past 10 years, eosinophilic esophagitis (EoE) has become a major cause of gastrointestinal symptoms, including dysphagia and food impaction in adolescents and adults, and feeding intolerance, failure to thrive, regurgitation, heartburn, and vomiting in children.

  • EoE is a clinicopathologic condition, so the entire clinical and histologic picture must be considered in making a diagnosis; no single feature is diagnostic on its own.

  • EoE is now diagnosed based on consensus guidelines

Patient history

EoE has been described throughout the world including North America, Europe, South America, Australia, and Asia, but the prevalence appears to be highest in the United States and Western Europe in comparison with Japan and China.9, 10, 19, 24, 25, 26 It also occurs in patients of all ages,1, 27, 28 but is more frequent in children and adults younger than 40 years.27, 28, 29 For reasons that are not understood, EoE is seen 3 to 4 times more frequently in males than in females, and is also more

Endoscopic features

Upper endoscopy is required for evaluation of clinical symptoms of EoE, assessment for other possible causes, and performance of esophageal biopsies. Multiple characteristic endoscopic findings of EoE have been reported,1, 52, 53, 54 but in up to 10% of cases the esophageal mucosa can appear normal, and biopsies are required or the diagnosis will be missed.55 These findings have a fair to good interobserver and intraobserver reliability,56, 57 and efforts are under way to standardize reporting

Histologic features

Infiltration of the esophageal mucosa with eosinophils is the histologic hallmark of EoE.65, 66 At present, finding at least 15 eosinophils per high-power microscopy field (eos/hpf) is suggestive of EoE.1 However, as discussed in more detail later, the finding of esophageal eosinophilia on biopsy is not specific for EoE. When biopsy samples are examined, in addition to the eosinophil count, which by convention represents the peak value in the most highly inflamed area on the biopsy, other

Consensus Guidelines

Because of heterogeneity in disease definition and reporting of data pertaining to EoE,28, 67, 68 an initial set of diagnostic guidelines was proposed in 2007 and represented a major step forward for the field.69 These guidelines have been recently updated after taking into account advances in understanding and complexities related to diagnosis.1 In this most recent document, EoE is defined conceptually as a “chronic immune/antigen-mediated esophageal disease characterized clinically by

Treatment

There are now several evidence-based treatment options for EoE. Pharmacologic agents are commonly used, but nonpharmacologic approaches such as dietary elimination therapy and endoscopy dilation are also effective. Of note, there are currently no medications for EoE approved by the Food and Drug Administration, so all pharmacologic treatment options are off-label. The overall goal of treating patients with EoE is to improve symptoms and normalize the esophageal mucosa without adversely

Treatment nonresponse

Whereas most patients respond to medical or dietary therapy, there are some who remain refractory to therapy. In these cases, a systematic assessment should be made to identify the reason for nonresponse, specifically determining whether ongoing esophageal eosinophilia is the cause of symptoms or if there are other contributing factors. Potential reasons for nonresponse include:

  • Nonadherence to the prescribed treatment.

  • Inadequate dosing of a topical steroid.

  • Candidal esophagitis complicating

Summary

EoE is a chronic allergen-mediated disorder defined by symptoms of esophageal dysfunction and epithelial eosinophilia on biopsy. It has rapidly emerged as an important cause of upper gastrointestinal morbidity in patients of all ages, and is encountered in a substantial proportion of patients undergoing diagnostic upper endoscopy.

Diagnosis of EoE is based on consensus guidelines, but can be challenging because none of the symptoms, endoscopic findings, or histologic features are specific for

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    This work was supported in part by NIH award number 1K23 DK090073-01.

    Disclosures: There are no conflicts of interested pertaining to this article. Dr Dellon has received research support from AstraZeneca, Meritage Pharma, Olympus, NIH, ACG, AGA, and CURED Foundation. Dr Dellon has been a consultant for Oncoscope.

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