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[Mimetics of systemic sclerosis].
Z Rheumatol
February 2019
Klinik für Rheumatologie und klinische Immunologie, Universitätsklinikum Schleswig-Holstein, Campus Lübeck, Ratzeburger Allee 160, 23538, Lübeck, Deutschland.
Background: Systemic sclerosis (SSc) is characterized by heterogeneous clinical symptoms. Peripheral skin fibrosis can be a common symptom. Nevertheless, a variety of diseases with different etiologies are associated with a thickening of the skin and make the initial diagnosis of systemic sclerosis more difficult.
View Article and Find Full Text PDF[Eosinophilia heralding the diagnosis of eosinophilic fasciitis (Shulman's disease)].
Rev Med Interne
December 2017
Service de médecine interne, hôpital Nord, Aix-Marseille université, Assistance publique-Hôpitaux de Marseille (AP-HM), chemin des Bourrely, 13915 Marseille cedex 15, France. Electronic address:
Introduction: Eosinophilic fasciitis or Shulman's disease is characterized, in its typical form, by palpable thickening of the skin and soft tissues, blood hypereosinophilia and fascia lesions. We hereby report a case of eosinophilic fasciitis in which hypereosinophilia preceded for several months the clinical signs of fasciitis.
Case Report: A 64-year-old woman, with a history of Little's syndrome with motor disability, was admitted in internal medicine for eosinophilia.
Idiopathic eosinophilic synovitis of the knee joint with peripheral eosinophilia - a rare case report.
J Clin Diagn Res
January 2015
Professor & Head, Department of Pathology, Saveetha Medical College, Thandalam, Chennai, India .
Synovitis, presenting as a synovial effusion is common. The most common cause include tuberculosis, osteoarthritis. Here with, presenting a rare case of monoarticular synovitis with synovial fluid and peripheral blood eosinophilia of unknown aetiology in an 18-year-old male.
View Article and Find Full Text PDF[Eosinophilic fasciitis, morphea and vitiligo in a single patient].
Ann Dermatol Venereol
October 2014
Service de dermatologie, CHU Hassan II, BP 1835, Atlass, Fès, Maroc.
Background: Fasciitis with eosinophilia (FE), or Shulman syndrome, is a rare disease of unknown origin for which the nosological profile has not been clearly defined. It is clinically characterised by oedema and induration of the limbs with hypereosinophilia. It may be associated with morphea, in which case it carries a poor prognosis, or other diseases, particularly autoimmune conditions.
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