Results 131 to 140 of about 61,675,345 (173)
A Familial Case of Scleroderma en Coup de Sabre
Acta Dermato-Venereologica, 2000 openaire +1 more source
Localized scleroderma en coup de sabre in the Neurology Clinic [PDF]
Multiple Sclerosis and Related Disorders, 2016 Localized scleroderma en coup de sabre (LScs) is a form of localized scleroderma thought to be an autoimmune disorder. Central nervous system involvement is not rare and neurological manifestations include seizures, focal neurological deficits, headache and neuropsychiatric changes.Patients attending the Neurology Clinic with the final diagnosis of ...
Esmeralda Lourenço +2 more
exaly +5 more sources
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International Journal of Dermatology, 2002
A man born in 1961 was apparently well until his marriage in May 1986. In August of that year, his attention was drawn to the presence of a reddish patch over the right forehead. It was initially asymptomatic. It continued to progress to form an apparent linear furrow extending from the receding hairline to the vertex and temporal part of the scalp. At
Virendra N, Sehgal +2 more
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A man born in 1961 was apparently well until his marriage in May 1986. In August of that year, his attention was drawn to the presence of a reddish patch over the right forehead. It was initially asymptomatic. It continued to progress to form an apparent linear furrow extending from the receding hairline to the vertex and temporal part of the scalp. At
Virendra N, Sehgal +2 more
openaire +2 more sources
Annals of Plastic Surgery, 1983
Five cases of scleroderma en coup de sabre are reported, along with a brief review of the literature [3, 10, 11]. Surgical management was tailored to the defects. Involved discolored skin was excised and the resultant wound repaired by direct closure (forehead, lower lip) or with full-thickness skin grafts.
M F, Milan, J E, Bennett
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Five cases of scleroderma en coup de sabre are reported, along with a brief review of the literature [3, 10, 11]. Surgical management was tailored to the defects. Involved discolored skin was excised and the resultant wound repaired by direct closure (forehead, lower lip) or with full-thickness skin grafts.
M F, Milan, J E, Bennett
openaire +2 more sources
Linear scleroderma “En Coup de Sabre” of the cheek
Journal of Oral and Maxillofacial Surgery, 2003Linear scleroderma (LS) is a variant of localized scleroderma most commonly seen in the lower limbs and to a lesser extent in the arms and face.1 Systemic involvement in LS is extremely rare.1,2 The term “en coup de sabre” is used for linear scleroderma located in the temporoparietal region that produces sharp bordered furrowing with alopecia when ...
Demir, Y +4 more
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Late-onset en coup de sabre of the skull
Skeletal Radiology, 2013En coup de sabre is a rare subtype of linear scleroderma that characteristically affects the skin, underlying muscle, and bone of the frontoparietal region of the face and scalp. It typically presents in the first two decades of life, and may be associated with focal neurological deficits. We present a case of late-onset en coup de sabre of the frontal
Shaun V, Mohan +2 more
exaly +3 more sources
Bilateral En Coup de Sabre—A Rare Entity
Pediatric Dermatology, 2000Abstract: Linear scleroderma involving the frontal or frontoparietal region of the scalp (with or without associated facial hemiatrophy) is called “en coup de sabre” (like the stroke of a sabre). We report a case which to the best of our knowledge is only the fifth instance of this subset of localized morphea occurring in a bilateral distribution.
R, Rai, S, Handa, S, Gupta, B, Kumar
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Management Options for Linear Scleroderma (“En Coup de Sabre”)
Dermatologic Surgery, 2022BACKGROUND En coup de sabre (ECDS) is a form of linear-scleroderma, primarily affecting the face. Despite effectiveness of pharmacological interventions in the management of lesions, sequelae of cutaneous deformities are common.
Ron, Skorochod +2 more
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Atypical Cases of Scleroderma en Coup de Sabre
Journal of Child Neurology, 2014Scleroderma en coup de sabre typically presents with a cutaneous induration, but involvement of the underlying bone, eye, and brain is common. We report on 4 pediatric cases with atypical initial clinical presentations. All cases were seen at the University of California San Francisco.
Verena, Kraus +7 more
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