Results 111 to 120 of about 9,361 (150)
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Linear scleroderma: A Neuman nursing perspective

Journal of Pediatric Nursing, 2000
Although 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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Laparoscopic Sleeve Gastrectomy for Linear Scleroderma

Journal of Laparoendoscopic & Advanced Surgical Techniques, 2010
Abstract Linear scleroderma is a rare type of autoimmune connective-tissue disorder and is one of five known types of localized, nonsystemic scleroderma. This type of localized scleroderma affects the skin and subcutaneous tissues and induces extensive fibrosis and atrophy of the affected limbs.
Jason, Kasza   +4 more
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Antihistone antibodies in linear scleroderma variants

International Journal of Dermatology, 2006
Background  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, 2019
Purpose 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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LINEAR SCLERODERMA

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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Localized forms of scleroderma, including morphea, linear scleroderma, and eosinophilic fasciitis

Current Opinion in Rheumatology, 1996
Under 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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Linear scleroderma

Archives of dermatology and syphilology, 2011
S, ROTHMAN, A L, SHAPIRO
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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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Immunologic Abnormalities in Linear Scleroderma

Archives of Dermatology, 1986
To the Editor.— In the November 1985 issue of theArchives, Woo et al 1 reported the results of their serologic study in linear scleroderma. Previously, Falanga et al 2 reported high titers of antibodies to single-stranded DNA in this disease. We have had a related case in our department, with some findings that we consider important to communicate ...
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Linear Melorheostotic Scleroderma With Hypertrichosis

Archives of Dermatology, 1979
On the basis of clinical features and histological findings, cutaneous manifestations of linear melorheostotic scleroderma are apparently derived from a localized proliferative disorder and are not secondary to bone changes. If the hypertrichosis has the same origin as the osteocutaneous changes, melorheostosis may represent a congenital disorder with ...
openaire   +1 more source

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