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Updated: Feb 16, 2026

Author Spotlight: Investigating the Pathophysiology of Eosinophilic Esophagitis
Published on: May 10, 2024
[EOSINOPHILIC FASCIITIS (EF)]
Avi Ben Shabat1, Gil Amarilyo2, Jerry Stein3
1Sackler Faculty of Medicine, Tel Aviv University.
Introduction:
Eosinophilic fasciitis (EF) is a rare connective tissue disease characterized by erythema, edema and myalgia with induration and thickening of the skin and soft tissue, especially subcutaneous fascia. Laboratory findings usually show peripheral eosinophilia, and full-thickness wedge biopsy is essential to establish the diagnosis. Corticosteroids are effective and remain the standard therapy for EF, although some patients may improve spontaneously. In this article we report a case of a 17 years old male who has been diagnosed with EF 2 years after bone marrow transplantation and review the clinical manifestations, pathology, diagnosis, differential diagnosis, and treatment of EF.
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