Abstract
<h3>To the Editor.—</h3> Eosinophilic fasciitis (EF) is characterized by sclerodermalike changes associated with peripheral blood eosinophilia, hypergammaglobulinemia, and an elevated erythrocyte sedimentation rate.<sup>1</sup>Since the first description by Shulman in 1974,<sup>2</sup>over 200 patients with EF have been described. Whether EF is a variant of scleroderma or a separate disease entity is still unclear. Multiple plaques of morphea developed in our patient 1 year after EF was diagnosed, which suggests a possible relationship between the two disorders. <h3>Report of a Case.—</h3> In January 1989, a 62-year-old white woman with a history of osteoarthritis was referred to the outpatient clinic of our department because of pain and stiffness in the skin of her lower extremities. She had not taken any drugs or L-tryptophan. On examination, the skin of her lower extremities was edematous and indurated. A full-thickness (down to underlying muscle) biopsy specimen from the upper leg revealed a
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Schedule a callDisclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.
