Results 11 to 20 of about 61,675,345 (173)

Scleroderma en coup de sabre treated with polymethylmethacrylate - Case report [PDF]

open access: yesAnais Brasileiros de Dermatologia, 2016
The scleroderma en coup de sabre is a variant of localized scleroderma that occurs preferentially in children. The disease progresses with a proliferative and inflammatory phase and later atrophy and residual deformity, which are treated with surgical ...
Joanna Pimenta de Araujo Franco   +4 more
doaj   +3 more sources

Dacryoadenitis associated with linear scleroderma en coup de sabre: A case report and review of literature [PDF]

open access: yesSkin Health and Disease
Dacryoadenitis in the setting of linear scleroderma en coup de sabre (LScs) is an association that has not previously been described in the scientific literature.
Eva Oustabassidis   +3 more
doaj   +3 more sources

Progressive Hemifacial Atrophy and Linear Scleroderma En Coup de Sabre: A Spectrum of the Same Disease? [PDF]

open access: yesFrontiers in Medicine, 2018
Similar clinical and histhopathological features in progressive hemifacial atrophy and linear scleroderma en coup de sabre are well known. Trauma may predispose to the development of both diseases.
Irina Khamaganova
doaj   +3 more sources

Bilateral Morphea en coup de sabre. A Rare Presentation [PDF]

open access: yesIndian Journal of Dermatology, 2021
Pablo Vargas-Mora   +3 more
doaj   +4 more sources

Brain cavernomas associated with en coup de sabre linear scleroderma: Two case reports [PDF]

open access: yesPediatric Rheumatology Online Journal, 2011
Linear scleroderma is a form of localized scleroderma that primarily affects the pediatric population. When it occurs on the scalp or forehead, it is termed "en coup de sabre".
Laxer Ronald M   +5 more
doaj   +2 more sources

Bony Hyperplasia Beneath Atrophic Soft Tissue: A Rare Case of En Coup de Sabre and Literature Review [PDF]

open access: yesClinical, Cosmetic and Investigational Dermatology, 2023
Xuda Ma,1,* Jiuzuo Huang,1,* Yu Chen,2 Xiaojun Wang,1 Xiao Long1 1Department of Plastic Surgery, Peking Union Medical College Hospital, Peking Union Medical College and Chinese Academy of Medical Sciences, Beijing, People’s Republic of China ...
Ma X, Huang J, Chen Y, Wang X, Long X
doaj   +2 more sources

Neurologic Involvement in Scleroderma en Coup de Sabre [PDF]

open access: yesAutoimmune Diseases, 2012
Localized scleroderma is a rare disease, characterized by sclerotic lesions. A variety of presentations have been described, with different clinical characteristics and specific prognosis. In scleroderma en coup de sabre (LScs) the atrophic lesion in frontoparietal area is the disease hallmark. Skin and subcutaneous are the mainly affected tissues, but
Tiago Nardi Amaral   +5 more
openaire   +4 more sources

Linear Scleroderma “En Coup De Sabre”: Initial Presentation as Intractable Partial Seizures in a Child

open access: yesPediatrics and Neonatology, 2009
Linear scleroderma is a form of localized scleroderma characterized by sclerotic lesions distributed in a linear, band-like pattern. The “en coup de sabre” subtype of linear scleroderma is more often associated with systemic morbidity, including ocular ...
Kuo-Liang Chiang   +3 more
doaj   +2 more sources

En coup de sabre.

open access: yesCutis, 2019
En coup de sabre (ECDS) is a rare form of localized scleroderma that typically manifests in children and women. It presents as a fibrous pansclerotic plaque extending in a bandlike distribution on the frontoparietal scalp with surrounding scarring alopecia.
Paul M, Graham   +2 more
core   +3 more sources

Magnetic resonance imaging findings in children with Parry-Romberg syndrome and en coup de sabre [PDF]

open access: yesPediatric 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   +2 more sources

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