Abstract

Characteristics of chronic milk-dependent food protein-induced enterocolitis syndrome (FPIES) in children from the region of Western Pomerania were studied. Prospectively, 55 children were diagnosed at a median of 2.2 months. The open food challenges (OFC), morphologies, milk-specific IgE (sIgE) (FEIA method, CAP system), and skin prick tests (SPTs) were examined. Vomiting and diarrhea escalated gradually but quickly led to growth retardation. Of the infants, 49% had BMI < 10 c, 20% BMI < 3 c; 25% had anemia, and 15% had hypoalbuminemia. During the OFCs we observed acute symptoms that appeared after 2–3 h: vomiting diarrhea and pallor. A total of 42% children required intravenous hydration. Casein hydrolysates or amino acids formulae (20%) were used in treatment. In 25% of children, SPT and milk sIgE were found, in 18%—other food SPTs, and in 14% allergy to other foods. A transition to IgE-dependent milk allergy was seen in 3 children. In the twelfth month of life, 62% of children had tolerance to milk, and in the twenty-fifth month—87%. Conclusions. Chronic milk-dependent FPIES resolves in most children. By the age of 2 children are at risk of multiple food sensitization, and those who have milk sIgE are at risk to transition to IgE-mediated milk allergy. Every OFC needs to be supervised due to possible severe reactions.

Highlights

  • Cow’s milk allergy (CMA) is the most common allergy in the first year of life

  • food protein-induced enterocolitis syndrome (FPIES) was diagnosed in these children, with a delayed response during open food challenges (OFC), in whom occurred vomiting, pallor, and diarrhea, and often severe dehydration

  • Symptoms of CMA appeared after cessation of breastfeeding and introduction of milk formula (80% of children) or mixed feeding (20% of children)

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Summary

Introduction

Cow’s milk allergy (CMA) is the most common allergy in the first year of life. It takes two forms: the IgE-mediated CMA (IgE-CMA) and the non-IgE mediated CMA (non-IgE-CMA). In contrast to IgE-CMA, the diagnosis of various non-IgE-CMA syndromes can be challenging due to the overall lack of noninvasive confirmatory testing for these disorders. Many of the non-IgE-CMA syndromes are diagnosed clinically based on history, diagnostic milk-free diet, and followed by positive milk provocation test, which is a “gold standard” for diagnosing these diseases [1,2]. The first classification of non-IgE-CMA gastrointestinal disorders was proposed by Sampson HA in 2003 [3]. It covers three items: food protein-induced enterocolitis syndrome (FPIES), food protein-induced allergic proctocolitis (FPIAP), and food protein-induced enteropathy syndrome (FPIE) as well as the syndrome of eosinophilic gastrointestinal diseases (EGID), where milk can cause allergic reactions under the IgE-dependent and IgE-independent mechanism

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