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[EOSINOPHILIC FASCIITIS (EF)].
Ben Shabat, Avi; Amarilyo, Gil; Stein, Jerry; Harel, Liora.
Afiliación
  • Ben Shabat A; Sackler Faculty of Medicine, Tel Aviv University.
  • Amarilyo G; Pediatric Rheumatology, Schneider Children's Medical Center of Israel.
  • Stein J; Bone Marrow Transplantation Department, Schneider Children's Medical Center of Israel.
  • Harel L; Sackler Faculty of Medicine, Tel Aviv University.
Harefuah ; 156(12): 786-790, 2017 Dec.
Article en He | MEDLINE | ID: mdl-29292619
ABSTRACT

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.
Asunto(s)
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Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Corticoesteroides / Eosinofilia / Fascitis Tipo de estudio: Diagnostic_studies Límite: Adolescent / Humans / Male Idioma: He Revista: Harefuah Año: 2017 Tipo del documento: Article
Buscar en Google
Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Corticoesteroides / Eosinofilia / Fascitis Tipo de estudio: Diagnostic_studies Límite: Adolescent / Humans / Male Idioma: He Revista: Harefuah Año: 2017 Tipo del documento: Article