Autor: |
Sahana M Srinivas, Pooja G Chebbi, Sanjay K Shivappa |
Jazyk: |
angličtina |
Rok vydání: |
2023 |
Předmět: |
|
Zdroj: |
Indian Dermatology Online Journal, Vol 14, Iss 5, Pp 676-678 (2023) |
Druh dokumentu: |
article |
ISSN: |
2229-5178 |
DOI: |
10.4103/idoj.idoj_632_22 |
Popis: |
Hypereosinophilic syndrome is a myeloproliferative disorder characterized by abnormal accumulation of eosinophils in the blood or peripheral tissues. It is uncommonly seen in children. We describe a 14-year-old girl diagnosed with idiopathic hypereosinophilic syndrome presenting with recurrent, painful oral and genital ulcers, hepatosplenomegaly along with consistently high eosinophil count and leucocytosis. Genetic studies showed negative for FIPIL-PDGFRA fusion gene. Mucosal ulcers were recalcitrant to conventional therapy and responded well to thalidomide. |
Databáze: |
Directory of Open Access Journals |
Externí odkaz: |
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