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Two strange cases of hypereosinophilia and child's relapsing angio-oedema
S Accomando1, M Caserta, A Trizzino
1G. Di Cristina Children's Hospital, Department of Paediatric, University of Palermo, Palermo. salvoaccomando@hotmail.com
Insights
Two children with recurrent angioedema and hypodermitis were diagnosed with human cysticercosis. Elevated IgE and hypereosinophilia, despite negative allergy tests, indicated parasitic infection.
Area of Science:
- Pediatric Allergy and Immunology
- Infectious Diseases
- Parasitology
Background:
- Recurrent angioedema and hypodermitis can present diagnostic challenges in pediatric patients.
- Atopic conditions in family history may suggest allergic etiologies, but other causes should be considered.
- Distinguishing allergic reactions from parasitic infections requires comprehensive diagnostic approaches.
Observation:
- Two pediatric patients presented with recurrent angioedema and localized, transient hypodermic infiltrations.
- Clinical examinations revealed good nutritional status but significant laboratory abnormalities.
- Laboratory findings included marked hypereosinophilia and immunoglobulin E (IgE) levels exceeding ten times the normal range.
Findings:
- Standard allergy testing (prick tests) for common inhalant and food allergens yielded negative results.
- Enzyme-linked immunosorbent assay (ELISA) testing showed strong positivity for Taenia Solium metacestodes in both patients' sera.
- These findings strongly suggested a diagnosis of human cysticercosis.
Implications:
- Human cysticercosis should be considered in the differential diagnosis of pediatric angioedema and hypereosinophilia, especially with negative allergy tests.
- Parasitic infections can mimic allergic conditions, highlighting the importance of broad diagnostic considerations.
- Early diagnosis and treatment of cysticercosis are crucial to prevent potential neurological complications and long-term sequelae.
Abstract:
Two patients aged two and four years came to our observation with "angio-oedema" and relapsing hypodermitis. Atopic diseases were present in both family histories. The clinical examination of both children revealed a good nutritional status, the presence of angio-oedema with fleeting (48 hours max length) and localized hypodermic infiltrations. Amongst laboratory investigations, the blood cells count and the total count of Immunoglobulins showed hypereosinophilia and increased IgE levels over ten times the normal values. Prick tests for the most common inhalant and nutritive allergens were negative. A strong positivity of ELISA for Taenia Solium metacestodes on both sera samples suggested a diagnosis of human cysticercosis.
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