Results 101 to 110 of about 84,037 (249)
Sclerosing diseases of the skin
JDDG: Journal der Deutschen Dermatologischen Gesellschaft, Volume 23, Issue 10, Page 1282-1300, October 2025.Summary Sclerosing skin diseases comprise a group of distinct dermatological conditions characterized by fibrotic changes that may severely impair patients’ quality of life. These conditions often present with cutaneous manifestations and, in some cases, may extend to extracutaneous tissues, potentially resulting in significant morbidity and mortality.
Yasamin Kalantari +4 more
wiley +1 more source
Orthopedic Considerations with Eosinophilic Fasciitis: A Case Report and Literature Review
Case Reports in Orthopedics, 2012 Eosinophilic fasciitis (EF) or Shulman's disease is a very rare condition first described in 1974 by Dr. Shulman in patients with diffuse fasciitis and eosinophilia. Fewer than 300 cases have been reported worldwide in the past 35 years.
Jason Samona
doaj +1 more source
Eosinophilic fasciitis in a rhesus macaque [PDF]
Arthritis & Rheumatism, 1992 AbstractEosinophilic fasciitis (EF) is an inflammatory disorder in the category of scleroderma‐like connective tissue diseases. There are no animal models for spontaneously occurring EF. We present the case of a rhesus macaque (Macaca mulatta) with clinical, laboratory, and histologic features of EF.
Edwin Klein, Scott T. Anderson
openaire +3 more sources
Diagnostic Reasoning in Surgical Pathology
Journal of Evaluation in Clinical Practice, Volume 31, Issue 5, August 2025.ABSTRACT Rationale Diagnostic reasoning in surgical pathology is critical for accurate disease identification, particularly for rare conditions. Despite advancements in methodologies, the diagnostic lag remains significant, highlighting the need for improved reasoning skills.
Ahti‐Veikko Pietarinen +1 more
wiley +1 more source
Eosinophilic fasciitis--progression to linear scleroderma: a case report
The Turkish Journal of Pediatrics, 1999 Eosinophilic fasciitis is a rare disease in children. Although changes similar to linear scleroderma have been reported, the outcome is usually good. In this report, a 10-year-old boy who developed eosinophilic fasciitis without a good response to
A Balat +4 more
doaj
Innovative Surgical Sciences, 2017 A 46-year-old man presented with clinical signs of nerve compression syndrome of his right ulnar nerve as confirmed by nerve conduction studies. Unexpectedly, clinical examination and magnetic resonance imaging (MRI) revealed a subcutaneous tumor of 5×2 ...
Thönnes Simon +3 more
doaj +1 more source
Systemic sclerosis without antinuclear antibodies or Raynaud's phenomenon: a multicentre study in the prospective EULAR Scleroderma Trials and Research (EUSTAR) database [PDF]
, 2017 Objective. To assess patients with SSc who present without circulating ANAs or RP. Methods. Five thousand three hundred and ninety patients who fulfilled the ACR criteria for SSc and were enrolled in the EULAR Scleroderma Trials and Research (EUSTAR ...
Carreira, Patricia E. +9 more
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, 2005 Eosinophilic fasciitis is a rare condition that presents with skin thickening involving extremities and sparing of the hands.It is a mimicker of Systemic sclerosis. Raynaud's phenomenon, ILD and other features associated with Systemic sclerosis are usually absent.It is characterised by eosinophilia and infiltration of skin and subcutaneous tissue by ...
Singh, Yogesh +4 more
openaire +1 more source
Muscle Vasculitis: A Novel Delineation of Distinct Subsets of Disease
ACR Open Rheumatology, Volume 7, Issue 6, June 2025.Objective The objective of this study was to assess the clinical and histopathologic features of muscle vasculitis. Methods The electronic database of SA Pathology, wherein all muscle biopsy samples in South Australia are assessed, was searched (2000–2023), identifying cases of vasculitis.
Thomas Khoo +4 more
wiley +1 more source
Hipertricosis adquirida y localizada en fascitis eosinofílica [PDF]
, 2013 La fascitis eosinofílica, se caracteriza por cambios cutáneos símil- esclerodermia y eosinofília periférica. Describimos un paciente de 54 años, de sexo masculino con diagnóstico de fascitis eosinofílica y seguimiento de 44 meses. Presentaba tumefacción,
Abaca, Héctor E. +1 more
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