Ann Clin Case Rep | Volume 7, Issue 1 | Case Report | Open Access

A Common but an Unusual Disease in a Child with Eosinophilia

Gökcan Öztürk1*, Tutku Parlar1, Şule Haskoloğlu2, Kübra Baskın2, Nazlı Deveci2, Ergin Çiftçi3, Figen Doğu2 and Aydan İkincioğulları2

1Department of Pediatric Health and Diseases, Ankara University School of Medicine, Turkey 2Department of Pediatric Immunology and Allergy, Ankara University School of Medicine, Turkey 3Department of Pediatric Infectious Diseases, Ankara University School of Medicine, Turkey

*Correspondance to: Gökcan Öztürk 

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Abstract

Hypereosinophilia is generally described as having an absolute eosinophil count of more than 500/mm3 in peripheral blood. 500-1500/mm3 is classified as mild, 1500-5000/mm3 as moderate, 5000/mm3 and above as severe eosinophilia. The causes of eosinophilia in children are similar to those seen in adults and it is separated into two groups as primary and secondary eosinophilia. Primary eosinophilia includes some genetic conditions such as hereditary eosinophilic syndrome. Secondary eosinophilia develops as a reaction to a certain cause. Among possible causes of secondary eosinophilia, we can list infections, atopy, medications, gastrointestinal diseases, lymphocytic diseases, and immunodeficiencies. In this paper, we discuss the differential diagnosis of hypereosinophilia in a 3-month-old girl presenting with generalized seborrheic dermatitis, hypereosinophilia, CMV viremia and pneumonia.

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Citation:

Öztürk G, Parlar T, Haskoloğlu Ş, Baskın K, Deveci N, Çiftçi E, et al. A Common but an Unusual Disease in a Child with Eosinophilia. Ann Clin Case Rep. 2022; 7: 2196..

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