Eosinophilic gastritis in children: current state of the problem. A review of the literature
REVIEWS
Abstract
Eosinophilic gastritis is a rare chronic, immune-mediated disorder belonging to the group of eosinophilic gastrointestinal diseases, whose incidence has increased over the past decade, including in children. Eosinophilic gastritis is characterized by nonspecific symptoms of upper gastrointestinal tract involvement and eosinophilic infiltration of the gastric wall at varying depths. The prevalence of eosinophilic gastritis in children is estimated at 7.1–17.6 per 100,000, with a peak incidence at age 5 years. Th2-mediated inflammation induced by food allergens plays a key role in its pathogenesis, as evidenced by its high comorbidity with atopy and the effectiveness of elimination diets. The clinical presentation varies from dyspeptic symptoms with mucosal involvement to signs of pyloric stenosis with muscularis infiltration. Diagnosis is based on histological examination of multiple biopsies (at least four from the corpus and antrum). According to the 2024 consensus, the diagnostic threshold for gastric ulceration is the presence of ≥30 eosinophils per high-power field. Endoscopic findings are often nonspecific, and normal-appearing mucosa does not exclude the diagnosis and requires biopsy even from intact areas. Elemental or empirical elimination diets are considered first-line treatment for young children. Topical (budesonide) or systemic corticosteroids are used to induce and maintain remission. A promising approach is the use of biological therapy, particularly dupilumab (a monoclonal antibody to the IL-4α receptor). Its efficacy in combined forms of eosinophilic gastritis has been demonstrated in several studies. However, its role in isolated eosinophilic gastritis requires clarification in randomized controlled trials. Since eosinophilic gastritis is a rare disease with no pathognomonic clinical symptoms or endoscopic changes, there are currently no uniform standards for diagnosis, differential diagnosis, treatment, or follow-up. Currently, the approach to managing such patients is individualized, taking into account the severity of the condition, which is determined based on a combination of data. Based on an analysis of current literature, this article presents data on the prevalence, pathogenesis, main clinical manifestations, laboratory, endoscopic, and histological changes, and treatment approaches.
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