Results 81 to 90 of about 85,574 (254)

Emerging Topical and Systemic JAK Inhibitors in Dermatology [PDF]

open access: yes, 2019
Accumulating data on cellular and molecular pathways help to develop novel therapeutic strategies in skin inflammation and autoimmunity. Examples are psoriasis and atopic dermatitis, two clinically and immunologically well-defined disorders.
Ghoreschi, Kamran   +2 more
core   +1 more source

Clinicopathological Challenge: A Progressively Enlarging Hardened Skin Plaque

open access: yesInternational Journal of Dermatology, Volume 65, Issue 1, Page 15-17, January 2026.
ABSTRACT Stiff skin syndrome (SSS) is a rare connective tissue disease manifesting as a progressive, non‐inflammatory fibrosis that causes the skin and soft tissues to harden. It can result in restricted joint movement, particularly affecting the shoulder and pelvic girdle. A segmental variant with a better prognosis has been described.
Marian Fernández Martínez   +3 more
wiley   +1 more source

Fascitis eosinofílica. A propósito de 13 casos [PDF]

open access: yes, 2012
Es tracta de la descripció d'una sèrie de 13 pacients amb fascitis eosinofílica diagnosticats en un hospital universitari entre 1989 i 2009. És una síndrome esclerodermiforme que es caracteritza per induració cutània i engruiximent i inflamació de la ...
Grados Cànovas, Maria Dolors   +2 more
core  

Identification of fetal DNA and cells in skin lesions from women with systemic sclerosis [PDF]

open access: yes, 1998
BACKGROUND: Systemic sclerosis is a disease of unknown origin which often occurs in women after their childbearing years. It has many clinical and histopathological similarities to chronic graft-versus-host disease.
Appleton AL   +15 more
core   +2 more sources

Solitary Fibrous Tumors of the Submandibular Gland: A Case Report

open access: yesClinical Case Reports, Volume 13, Issue 12, December 2025.
ABSTRACT Solitary fibrous tumors (SFTs) are uncommon neoplasms that arise from the pleura. Although they can appear in various extrathoracic areas, they are uncommon in the submandibular gland. This paper reports a 37‐year‐old woman with a spherical, hypoechogenic mass measuring 13 × 37 mm and having a regular boundary on the left side of the ...
Maryam Garousi   +5 more
wiley   +1 more source

Eosinophilic fasciitis

open access: yesDermatology Online Journal, 2003
The case of a 76-year-old woman with eosinophilic fasciitis is presented. Reported etiologic associations and treatment options are discussed.
openaire   +4 more sources

Eosinophilic Fasciitis Associated with Myositis

open access: yesCase Reports in Dermatology, 2015
Eosinophilic fasciitis is clinically characterized by symmetrical scleroderma-like indurations of the skin with pain. The histological features are fascial inflammation with lymphocytes and eosinophils as well as thickened and fibrotic fascia ...
Yuko Adachi   +5 more
doaj   +1 more source

Focal Myositis in paediatric age. [PDF]

open access: yes, 2015
BACKGROUND: Focal Myositis is a rare pseudotumor of unknown aetiology that is often difficult to diagnose and treat. Typically afflicting people in adulthood, it has occasionally been reported also among children.
Alaggio, Rita, Corradin, M, Gigante, C
core   +1 more source

Large‐Bore Vacuum Suction Biopsy of Pediatric Soft Tissue Tumors: A 5‐Year Retrospective Analysis of Safety and Effectiveness

open access: yesPediatric Blood &Cancer, Volume 72, Issue 12, December 2025.
ABSTRACT Introduction Percutaneous large‐bore vacuum suction biopsy (LBVSB) is an innovative alternative to open surgical biopsy and minimally invasive image‐guided percutaneous core needle biopsy (PCNB) for pediatric soft tissue tumors. This study reviews our experience using this modality.
Abhinav R. Balu   +8 more
wiley   +1 more source

Eosinophilic fasciitis--progression to linear scleroderma: a case report

open access: yesThe 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  

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