Parasitic Hypereosinophilia in Childhood: a Diagnostic Challenge

Roberto Antonucci, Nadia Vacca, Giulia Boz, Cristian Locci, Rosanna Mannazzu, Claudio Cherchi, Giacomo Lai, Claudio Fozza

Research output: Contribution to journalArticle

Abstract

Severe hypereosinophilia (HE) in children is rare, and its etiological diagnosis is challenging. We describe a case of a 30-month-old boy, living in a rural area, who was admitted to our Clinic with a 7-day history of fever and severe hypereosinophilia. A comprehensive diagnostic workup could not identify the cause of this condition. On day 6, the rapidly increasing eosinophil count (maximum value of 56,000/mm3), the risk of developing hypereosinophilic syndrome, and the patient's history prompted us to undertake an empiric treatment with albendazole. The eosinophil count progressively decreased following treatment. On day 13, clinical condition and hematological data were satisfactory, therefore the treatment was discontinued, and the patient was discharged. Three months later, anti-nematode IgG antibodies were detected in patient serum, thus establishing the etiological diagnosis. In conclusion, an empiric anthelmintic treatment seems to be justified when parasitic hypereosinophilia is strongly suspected, and other causes have been excluded.

Original languageEnglish
Pages (from-to)e2018034
Number of pages4
JournalMediterranean Journal of Hematology and Infectious Diseases
Volume10
Issue number1
DOIs
Publication statusPublished - 2018
Externally publishedYes

Fingerprint Dive into the research topics of 'Parasitic Hypereosinophilia in Childhood: a Diagnostic Challenge'. Together they form a unique fingerprint.

  • Cite this

    Antonucci, R., Vacca, N., Boz, G., Locci, C., Mannazzu, R., Cherchi, C., Lai, G., & Fozza, C. (2018). Parasitic Hypereosinophilia in Childhood: a Diagnostic Challenge. Mediterranean Journal of Hematology and Infectious Diseases, 10(1), e2018034. https://doi.org/10.4084/MJHID.2018.034