Results 31 to 40 of about 65,412,535 (160)
Sclerosing diseases of the skin. [PDF]
J Dtsch Dermatol GesSummary 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.
Kalantari Y +4 more
europepmc +2 more sources
Linear alopecia in pediatrics: RCM and dermoscopy reveal diagnostic cues
Skin Research and Technology, Volume 29, Issue 11, November 2023., 2023 Abstract Background Alopecia areata (AA), trichotillomania (TM), nevus sebaceous (NS), and linear scleroderma en coup de sabre (LSCS) can all present with a patch of linear alopecia, making diagnosis challenging. The purpose of this study was to combine reflectance confocal microscopy (RCM) and dermoscopy in the diagnosis of these lesions in children ...
Ying Wang +3 more
wiley +1 more source
Role of imaging in morphea assessment: A review of the literature
Skin Research and Technology, Volume 29, Issue 7, July 2023., 2023 Abstract Background Localized scleroderma, known as morphea, is a connective tissue disorder characterized by inflammation and fibrosis of the skin and the soft tissue. There exist no universally accepted validated outcome measures in order to monitor the disease activity.
Faezeh Khorasanizadeh +2 more
wiley +1 more source
Enhancing Hair Regrowth in Pediatric Morphea en Coup de Sabre by Fractional CO2 Laser-Assisted Exosome Delivery. [PDF]
J Cosmet DermatolJournal of Cosmetic Dermatology, Volume 24, Issue 6, June 2025.
Ahuja R, Huang PP.
europepmc +2 more sources
BMC Neurology, 2009 Background Hemifacial atrophy (Parry-Romberg syndrome) is a relatively rare disease. The etiology of the disease is not clear. Some authors postulate its relation with limited scleroderma linearis.
Brzezińska-Wcisło Ligia +2 more
doaj +1 more source
, 2021 Scleroderma (morphea) en coup de sabre is a localized subtype restricted to the frontoparietal region of the head. Current treatment paradigms rely on low levels of evidence, primarily case reports and case series-supported by expert opinions. The aim of
Małgorzata Olszewska +5 more
core +1 more source
Ophthalmic findings in linear scleroderma manifesting as facial en coup de sabre [PDF]
Eye, 2018 To evaluate ophthalmic involvement in a long-term series of patients with en coup de sabre (ECS) close to the eye based on the hypothesis that this is not commonly affected, or simply under-reported.An observational study of ophthalmological findings in patients from Copenhagen University Dermatology Clinics. A standard eye examination further included
Hans Callø, Fledelius +2 more
openaire +2 more sources
Journal of Medical Case Reports, 2019 Background Parry–Romberg syndrome, also known as progressive hemifacial atrophy, is a rare degenerative disorder with numerous distinctive clinical presentations. It is usually slowly progressive, occurring more in females, and affects primarily one side
Jimmy Girgis William Abdelnour +3 more
doaj +1 more source
Magnetic resonance imaging findings in children with Parry-Romberg syndrome and en coup de sabre
Pediatric Rheumatology Online Journal, 2021 Background The aim of this study was to: (i) describe the abnormalities seen on brain imaging in a group of children with en coup de sabre (EDCS) with/without Parry-Romberg syndrome (PRS); and (ii) identify clinical predictors of brain imaging ...
Harry Knights +6 more
doaj +1 more source
Frontal linear scleroderma (en coup de sabre)
Dermatology Online Journal, 2003 En coup de sabre is a type of linear scleroderma that presents on the frontal or frontoparietal scalp. The case of a 54-year-old woman with a 3 and one-half year history of en coup de sabre is presented. The clinical presentation, laboratory findings, epidemiology, etiologic hypotheses, and treatment options are reviewed.
openaire +4 more sources