Hypereosinophilic syndrome with erythrodermia

Authors

  • Héctor Huayhua-Guevara Universidad Nacional Mayor de San Marcos
  • Miguel A. Vargas-Cruz Universidad Nacional Mayor de San Marcos
  • Chian-García César A. Universidad Peruana Cayetano Heredia

DOI:

https://doi.org/10.36393/spmi.v33i1.507

Keywords:

Eosinophilia, hypereosinophilia, skin, prednisone

Abstract

A 77-year-old male, with a history of heart failure and atrial fibrillation receiving warfarin, hypothyroidism, diabetes mellitus and hyperuricaemia, with a one-year history of erythematous and desquamative skin lesions in the trunk, pruritic and moderate recurrent eosinophilia. After allergic, parasitic, autoimmune and neoplastic causes were ruled out, the diagnosis of idiopathic hypereosinophilic syndrome was done. He was treated with prednisone and hydroxyurea, resulting in complete remission of eosinophilia and progressive improvement of dermal lesions.

Downloads

Download data is not yet available.

Published

2020-04-24

Issue

Section

Case report

How to Cite

Hypereosinophilic syndrome with erythrodermia. (2020). Revista De La Sociedad Peruana De Medicina Interna, 33(1), 25-30. https://doi.org/10.36393/spmi.v33i1.507