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Juvenile linear scleroderma with unique forms of renal involvement
Pediatric Nephrology, 2009 Linear scleroderma is the most common type of juvenile localized scleroderma, which usually involves the limbs. The linear lesions may extend through the dermis, subcutaneous tissue, muscles, and the underlying bone, leading to significant functional and
Belde Kasap +2 more
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Melorheostosis: Report of a new case with linear scleroderma
Clinical Rheumatology, 1998 Melorheostosis is a very rare bone disease of unknown etiology characterised by linear hyperostosis and associated with fibrosis of soft tissues and the skin.
M Birtane
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Melorheostosis With Linear Scleroderma
Archives of Dermatology, 1963The seventh case of linear scleroderma associated with melorheostosis is presented and the literature reviewed. Melorheostosis is a rare disorder of bone, first described in 1922. It is a peculiar, linear hyperostosis, usually in an extremity, that has been likened to the tallow drippings on the side of a burning candle.
S A, MULLER, E D, HENDERSON
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Linear scleroderma: A Neuman nursing perspective
Journal of Pediatric Nursing, 2000Although quite a rare pediatric disease, linear scleroderma (LS), a chronic disease, may leave scarring and may have devastating effects on a child and family. This article provides an overview of the disease, presents a case history of a boy with LS, and discusses how nurses and other health-team members assisted the child and family in managing the ...
C C, Fuller, B, Hartley
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Antihistone antibodies in linear scleroderma variants
International Journal of Dermatology, 2006Background Linear scleroderma occurs as two clinically distinct variants: the frontoparietal en coup de sabre type, and the torso‐extremity type. Antihistone antibodies (AHAs), which traditionally are markers for drug‐induced lupus, may also be linked to linear scleroderma.Methods Retrospective review of all patients presenting with linear ...
Rokea A, el-Azhary +4 more
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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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Archives of Dermatology and Syphilology, 1948
THE CAUSE of linear scleroderma is obscure. Several authors have been impressed by the fact that many lesions in this disease have a segmental distribution or follow the course of peripheral nerves. Therefore, they have assumed that linear scleroderma originates in the nervous system.
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THE CAUSE of linear scleroderma is obscure. Several authors have been impressed by the fact that many lesions in this disease have a segmental distribution or follow the course of peripheral nerves. Therefore, they have assumed that linear scleroderma originates in the nervous system.
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Localized forms of scleroderma, including morphea, linear scleroderma, and eosinophilic fasciitis
Current Opinion in Rheumatology, 1996Under the term localized scleroderma a spectrum of conditions is classified, ranging from localized plaques of morphea of cosmetic importance only, to deep lesions of linear scleroderma and eosinophilic fasciitis, which can result in considerable morbidity. The etiology is unknown; environmental, infectious, and autoimmune causes have been proposed. In
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Physiatrics for Deforming Linear Scleroderma
Archives of Dermatology, 1976• When linear scleroderma traverses several joints, severe and mutilating deformities and contractures, with loss of limb function, can result. Drugs and surgical procedures are usually of little benefit in ameliorating the deformities. Physiatrics, on the other hand, is a readily available modality that can restore much useful function and reverse the
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