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Diagnosis and management of linear scleroderma in children
Current Opinion in Pediatrics, 2019Purpose of review Linear scleroderma is the most common subtype of localized scleroderma (LoS) in children. It can be associated with extracutaneous manifestations and long-term sequelae. Thus, appropriate diagnosis and management are key to improve the prognosis.
Adriana G Peña-Romero+1 more
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Restrictive Ophthalmopathy Associated with Linear Scleroderma
Journal of Neuro-Ophthalmology, 1995A patient with a coup de sabre lesion of the forehead developed progressive ipsilateral limitation of ocular motility, primarily involving adduction and depression. Investigation disclosed no other explanation for the ocular motility disturbance, which we suspect represents restrictive myopathy maximally involving ocular muscles immediately subjacent ...
William W. Campbell, Frank J. Bajandas
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Linear scleroderma associated with progressive brain atrophy
Brain and Development, 2003Linear scleroderma (LS) is characterized by scleroatrophic lesions affecting limbs and legs, unilaterally. Neurological involvement may be associated with ipsilateral facial and skull involvement in disorders referred to clinically as LS 'en coup de sabre', and Parry-Romberg syndrome.
Grosso, S.+6 more
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A case of a childhood linear scleroderma with limb asymmetry
Modern Rheumatology, 2004We report the case of a child with unilateral linear scleroderma disturbing the right lower limb. It took three-quarters of a year to be diagnosed as linear scleroderma and another 8 months to be treated with oral steroids. Although functional disabilities of the right knee and foot were improved with the steroid therapy, the limb asymmetry has ...
Kazumitsu Sugiura+2 more
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Total hemiatrophy as a rare presentation of linear scleroderma
The Netherlands Journal of Medicine, 1995Scleroderma rarely presents as total hemiatrophy of one side of the body. A 63-year-old patient is discussed with progressive facial hemiatrophy and with atrophy of skin, subcutaneous tissue, muscle and bone tissue of one side of the body, complicated by ocular and neurological manifestations.
B. Bravenboer, W.H.E. Waale
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Lacrimal Drainage System Involvement in Linear Scleroderma
Ophthalmic Plastic & Reconstructive Surgery, 2017Linear scleroderma is a localized variety of scleroderma characterized by fibrotic areas of the dermis involving head region without systemic features. Ocular involvement has been sparsely reported in the form of episcleritis, dry eye, and uveitis. We describe a 42-year-old man with linear scleroderma, en coup de sabre type with associated nasolacrimal
Dilip Kumar Mishra+3 more
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Linear scleroderma as a cause for hemiatrophy [PDF]
Randy Rosenberg+2 more
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Severe Wrist Contracture in a Child With Linear Scleroderma
Annals of Plastic Surgery, 2001Linear scleroderma is an unusual disorder characterized by linear streaks of fibrotic skin involvement, which can lead to severe limb deformities and contractures. The authors present a case of severe wrist contracture in a child with linear scleroderma treated by release of the contracture with coverage of the exposed carpus with an abductor digiti ...
Rita Jerathmd, W. Glenn Lyle
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Melorheostosis: Report of a new case with linear scleroderma
Clinical Rheumatology, 1998Melorheostosis is a very rare bone disease of unknown etiology characterised by linear hyperostosis and associated with fibrosis of soft tissues and the skin. This uncommon sclerosing bone dysplasia was first described by Leri and Joanny in 1922, and since then, until 1993, approximately 300 cases were reported in the literature.
Fikret Tüzün+3 more
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Juvenile Linear Scleroderma Associated With Serologic Abnormalities
Archives of Dermatology, 1985We investigated 24 juvenile cases of linear scleroderma for the presence of systemic disease and serologic abnormalities. Thirteen of 24 patients had antinuclear antibodies (ANA) at titers of 1:40 or greater. Rheumatoid factor (titers greater than or equal to 1:20) was detected in seven of 17 patients tested, five of whom also had ANA.
James E. Rasmussen, Thomas Y. Woo
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