Hypereosinophilic Syndrome, Erythroderma as Clinical Debut. Case Report and Literature Review

Abstract

Eosinophilia is a common finding in clinical practice, but when elevated values of eosinophils are found, it constitutes a diagnostic challenge. Hypereosinophilic syndrome is a group of rare disorders defined by persistent blood hypereosinophilia >1.5 × 109/l and associated to organ damage that result in a wide variety of clinical manifestations: fatigue with nonspecific skin lesions, to endomyocardial fibrosis, neurological compromise and life-threatening evolution.The prognosis of the disease is variable and depends on the variant and the availability of specific treatment. 1-2We present the clinical case of a patient with a history of B symptoms and the presence of persistent erythroderma. The patient underwent several complementary studies, including skin biopsy without presenting a definitive diagnosis. Laboratory with persistence of hypereosinophilia that guided us towards the diagnosis ofIdiopathic Hypereosinophilic Syndrome

Authors and Affiliations

Polanco Llanes Alondra S, Salazar Quijano Christian A, Can Pérez Eric E,Arjona Bojorquez RashidI,Luna Garcia Javier, García Catalán Grisell, Alonzo Burgos Marcos A

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  • EP ID EP731733
  • DOI 10.47191/ijmscrs/v2-i7-10
  • Views 31
  • Downloads 0

How To Cite

Polanco Llanes Alondra S, Salazar Quijano Christian A, Can Pérez Eric E, Arjona Bojorquez RashidI, Luna Garcia Javier, García Catalán Grisell, Alonzo Burgos Marcos A (2022). Hypereosinophilic Syndrome, Erythroderma as Clinical Debut. Case Report and Literature Review. International Journal Of Medical Science And Clinical Research Studies, 2(07), -. https://europub.co.uk/articles/-A-731733