Eosinophilic fasciitis

Authors

  • Mayled María Delgado Molina San Martín de La Plata General Acute Interzonal Hospital, La Plata, Buenos Aires Province, Argentina
  • Marina Agriello San Martín de La Plata General Acute Interzonal Hospital, La Plata, Buenos Aires Province, Argentina
  • María De Los Ángeles Michelena San Martín de La Plata Interzonal General Acute Hospital, La Plata, Buenos Aires Province, Argentina
  • Gabriela Laura Arena San Martín de La Plata Interzonal General Acute Hospital, La Plata, Buenos Aires Province, Argentina

DOI:

https://doi.org/10.47196/da.v31i2.2867

Keywords:

fasciitis, eosinophilia, scleroderma

Abstract

Eosinophilic fasciitis is a scleroderma-like syndrome that involves the deep fascia and subcutaneous cellular tissue. It manifests with edema and symmetrical induration of the extremities that can progress to fibrosis and cause functional limitation. The diagnosis is made based on the clinical features, the results of histopathology and typical magnetic resonance imaging findings. The treatment of choice is systemic steroids. Three clinical cases assisted in our department are presented.

Author Biographies

Mayled María Delgado Molina, San Martín de La Plata General Acute Interzonal Hospital, La Plata, Buenos Aires Province, Argentina

Dermatology Resident

Marina Agriello, San Martín de La Plata General Acute Interzonal Hospital, La Plata, Buenos Aires Province, Argentina

Dermatology trainee

María De Los Ángeles Michelena, San Martín de La Plata Interzonal General Acute Hospital, La Plata, Buenos Aires Province, Argentina

Staff Physician of the Dermatology Service

Gabriela Laura Arena, San Martín de La Plata Interzonal General Acute Hospital, La Plata, Buenos Aires Province, Argentina

Head of the Dermatology Service

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Published

2025-08-01

Issue

Section

Original Articles