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Tracking Public Interest in Rare Diseases and Eosinophilic Disorders in Germany: Web Search Analysis
Diagnosis is typically based on the exclusion of other causes of eosinophilia (eg, allergic diseases or parasitic infections) and histopathological and immunohistochemical studies, permitting classification in the following subtypes: myeloproliferative (M-HES), lymphocytic (L-HES), idiopathic (I-HES), and chronic eosinophilic leukemia not otherwise specified (CEL-NOS). [1,10].
JMIR Infodemiology 2025;5:e69040
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Drug reaction with eosinophilia and systemic symptoms (DRESS) syndrome causes severe cutaneous and systemic complications with a mortality rate of ≈10% [1,2]. The current standard of care for DRESS syndrome involves the removal of the culprit drug, supportive therapy, and systemic corticosteroids. Corticosteroid therapy must be tapered for weeks to months to prevent DRESS syndrome relapse [1].
JMIR Dermatol 2023;6:e41391
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