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Allergic Proctocolitis: Literature Review and Proposal of a Diagnostic-Therapeutic Algorithm
Simona Barni1, Francesca Mori1, Mattia Giovannini1,2
1Allergy Unit, Meyer Children's Hospital IRCCS, 50139 Florence, Italy.
Insights
Allergic proctocolitis (AP), a non-IgE-mediated food allergy in infants, presents with blood in stool. Diagnosis involves food elimination and reintroduction, with most infants outgrowing the allergy by one year.
Area of Science:
- Pediatric Allergy and Immunology
- Gastroenterology
- Clinical Nutrition
Background:
- Allergic proctocolitis (AP) is an increasingly recognized non-IgE-mediated food allergy in infants.
- Clinical signs include hematochezia in otherwise healthy, thriving infants, often starting in early infancy.
- Cow's milk protein is the most common trigger, but other allergens like soy and egg can also be implicated.
Purpose of the Study:
- To provide an updated review of allergic proctocolitis.
- To offer current recommendations on epidemiology, diagnosis, and treatment.
- To aid pediatricians, allergists, and gastroenterologists in managing AP.
Main Methods:
- Diagnosis relies on clinical history and response to dietary elimination and challenge.
- Symptoms typically resolve within 72-96 hours after removing the trigger food.
- The review synthesizes current literature and clinical guidelines.
Main Results:
- Allergic proctocolitis is a benign and self-limiting condition.
- Most children tolerate the offending food antigen by one year of age.
- The long-term prognosis for affected infants is excellent.
Conclusions:
- Effective management of AP involves identifying and eliminating trigger foods.
- Early diagnosis and appropriate dietary management lead to symptom resolution.
- Children with AP generally have a favorable prognosis and outgrow the condition.
Abstract:
Allergic proctocolitis (AP) is a benign condition, frequent in childhood, that is classified as a non-IgE-mediated food allergy. The prevalence is unknown; however, its frequency appears to be increasing, especially in exclusively breastfed infants. Clinical manifestations typically begin in the first few months of life with the appearance of bright red blood (hematochezia), with or without mucus, in the stool of apparently healthy, thriving infants. Most cases of AP are caused by cow's milk proteins; however, other allergens, such as soy, egg, corn, and wheat, may be potential triggers. Diagnosis is based on the patient's clinical history and on the resolution of signs and symptoms with the elimination of the suspected food antigen from the diet and their reappearance when the food is reintroduced into the diet. The treatment of AP is based on an elimination diet of the trigger food, with resolution of the symptoms within 72-96 h from the beginning of the diet. The prognosis of AP is good; it is a self-limiting condition, because most children can tolerate the trigger food within one year of life, with an excellent long-term prognosis. The purpose of this review is to provide an update on the current knowledge and recommendations in epidemiological, diagnostic, and therapeutic terms to the pediatricians, allergists, and gastroenterologists who may find themselves managing a patient with AP.
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