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COATS-LIKE RESPONSE IN LINEAR EN COUP DE SABRE SCLERODERMA

RETINAL Cases & Brief Reports, 2011
To describe a Coats-like response and central nervous system vasculitis and its successful management in a patient presenting with en coup de sabre scleroderma.Retrospective interventional case report. Chart review.A 20-year-old white male patient with en coup de sabre scleroderma on treatment with oral cyclophosphamide and prednisone for associated ...
Mathew K, George   +2 more
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Linear scleroderma (morphoea) “en coup de sabre”

2008
Scleroderma is a rare connective tissue disorder of unknown etiology in which increased collagen deposition occurs and results in sclerosis of the skin and subcutaneous tissue (with dermal atrophy), often affecting the underlying muscle and bone (Sampaio et al. 2006).
PASCUAL CASTROVIEJO I, RUGGIERI, MARTINO
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Linear Scleroderma En Coup De Sabre

1999
We studied 58 cases of linear scleroderma of the face: 20 of them showed transition into progressive facial hemiatrophy (PFH). In several cases a distinction between these two conditions was not possible since the atrophic changes were arranged along the previous indurations, usually along the branches of trigeminal nerve.
Maria Blaszczyk, S. Jablonska
openaire   +1 more source

Orbital Myositis in a Child With Linear Scleroderma En Coup de Sabre

Journal of Pediatric Ophthalmology & Strabismus, 2007
info:eu-repo/semantics ...
Roulez, Françoise   +3 more
openaire   +2 more sources

Linear scleroderma ‘en coup de sabre’

Practical Neurology
Linear scleroderma ‘en coup de sabre’ is a rare condition characterised by inflammation and fibrosis of the skin and underlying tissues; it rarely presents in adults. The adult-onset form seldom has extracutaneous manifestations, but those that occur are usually neurological. A 43-year-old woman with epilepsy had a scar-like lesion on her forehead. The
Patxi Zavala Gottau   +11 more
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Bilaterale lineare temporoparietale Sklerodermie en coup de sabre

Der Hautarzt, 1994
Bilateral linear frontoparietal scleroderma en coup de sabre is an extremely rare form of localized linear scleroderma. In this paper the case of a 35-year-old woman with bilateral linear temporoparietal scleroderma en coup de sabre is presented. The manifestations that can be associated with linear scleroderma and the serologic abnormalities it ...
J U, Ostertag   +2 more
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Linear scleroderma ‘en coup de sabre’ associated with cerebral and ocular vasculitis

Scandinavian Journal of Rheumatology, 2006
Linear scleroderma 'en coup de sabre' (LSCS) has been reported in association with intracranial abnormalities. We report the case of an 11-year-old boy with LSCS who presented with recurrent headaches. Cranial magnetic resonance imaging (MRI) and angiography were consistent with the diagnosis of a cerebral vasculitis.
A, Holl-Wieden   +4 more
openaire   +2 more sources

Silent White Matter Lesion in Linear Scleroderma En Coup de Sabre

Journal of Computer Assisted Tomography, 2008
We report a patient with linear scleroderma en coup de sabre without neurological symptoms despite the presence of large white matter lesions. The patient underwent 3.0-T magnetic resonance (MR) examinations including diffusion tensor imaging, time-resolved contrast-enhanced MR angiography, susceptibility-weighted imaging, and proton MR spectroscopy ...
Mio, Sakai   +11 more
openaire   +2 more sources

Treatment of Linear Scleroderma ( en Coup de Sabre ) With Dermal Fat Grafting

Journal of Cutaneous Medicine and Surgery, 2015
Background: Linear scleroderma, also known as “ en coup de sabre,” is a subtype of localized scleroderma that warrants aesthetic correction because it appears on the forehead region in children. Objective: To report dermal fat grafting
CINAL, Hakan   +3 more
openaire   +3 more sources

Alopecia with perineural lymphocytes: a clue to linear scleroderma en coup de sabre

Journal of Cutaneous Pathology, 2012
Linear scleroderma en coup de sabre (‘the stroke of the sword’) is an uncommon form of morphea with onset typically in childhood or adolescence. Involvement is usually located on the paramedian forehead and is associated with alopecia. It is microscopically indistinguishable from other forms of scleroderma.
Carolyn, Goh   +2 more
openaire   +2 more sources

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