Results 231 to 240 of about 61,964 (279)
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Scleroderma Renal Crisis Prior to Scleroderma
American Journal of Kidney Diseases, 1989SCLERODERMA renal crisis (SRC) is characterized by rapid onset of severe hypertension and rapid deterioration of renal function. Although this event usually complicates established progressive systemic sclerosis (PSS), occasionally SRC may be the mode of presentation of the illness.
S F, Gouge +4 more
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Clinical Rheumatology, 2003
Progressive systemic sclerosis (PSS) can involve the skin diffusely or in a limited way. Rarely cutaneous involvement can assume a hypertrophic form, described in the literature as keloidal scleroderma. The authors describe a PSS patient who presented cutaneous manifestations compatible with the diagnosis of this clinical situation.
Mittermayer, Santiago +4 more
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Progressive systemic sclerosis (PSS) can involve the skin diffusely or in a limited way. Rarely cutaneous involvement can assume a hypertrophic form, described in the literature as keloidal scleroderma. The authors describe a PSS patient who presented cutaneous manifestations compatible with the diagnosis of this clinical situation.
Mittermayer, Santiago +4 more
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2008
The prototypic autoimmune diseases involving skin (lupus, dermatomyositis) typically result in epithelial injury and autoantibodies to characteristic cellular antigens. Disease-specific autoantibodies are also found in scleroderma, but scleroderma is different from other cutaneous autoimmune diseases because epithelial injury does not occur.
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The prototypic autoimmune diseases involving skin (lupus, dermatomyositis) typically result in epithelial injury and autoantibodies to characteristic cellular antigens. Disease-specific autoantibodies are also found in scleroderma, but scleroderma is different from other cutaneous autoimmune diseases because epithelial injury does not occur.
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Annals of Internal Medicine, 1991
To the Editors: Iloprost (Schering Corporation, Kenilworth, New Jersey), a stable prostacyclin analog, is a powerful vasodilator and platelet anti-aggregant.
T, Constans, E, Diot, G, Lasfargues
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To the Editors: Iloprost (Schering Corporation, Kenilworth, New Jersey), a stable prostacyclin analog, is a powerful vasodilator and platelet anti-aggregant.
T, Constans, E, Diot, G, Lasfargues
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Seminars in Immunopathology, 2015
Systemic sclerosis (SSc) is a multisystem connective tissue disorder featured by vascular injury and fibrosis of the skin and various internal organs with autoimmune background. Although the pathogenesis of SSc still remains elusive, it is generally accepted that initial vascular injury due to autoimmunity and/or environmental factors causes structural
Yoshihide, Asano, Shinichi, Sato
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Systemic sclerosis (SSc) is a multisystem connective tissue disorder featured by vascular injury and fibrosis of the skin and various internal organs with autoimmune background. Although the pathogenesis of SSc still remains elusive, it is generally accepted that initial vascular injury due to autoimmunity and/or environmental factors causes structural
Yoshihide, Asano, Shinichi, Sato
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Best Practice & Research Clinical Rheumatology, 2005
Juvenile scleroderma with its two varieties, juvenile localized scleroderma and systemic sclerosis (SSc), represents the third most frequent rheumatic disease in childhood. In juvenile SSc, new developments have been recently reported in the fields of classification and monitoring.
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Juvenile scleroderma with its two varieties, juvenile localized scleroderma and systemic sclerosis (SSc), represents the third most frequent rheumatic disease in childhood. In juvenile SSc, new developments have been recently reported in the fields of classification and monitoring.
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Melorheostosis with scleroderma
Clinical Imaging, 2004The association of linear scleroderma with melorheostosis is very rare. Until now, only a few cases have been reported in the English literature. We describe a case of melorheostosis of a rib associated with overlying skin changes.
G, Shivanand, D N, Srivastava
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Scleroderma and Pseudo-Scleroderma.
Archives of Internal Medicine, 1968This book appeared in Poland in 1963 and was translated for the National Library of Medicine in 1965. It is unlike most American textbooks, particularly as it takes an editorial stance and evaluates data from this perspective. The author favors the neurogenic theory, which is at variance with most American opinions.
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Rheumatic Disease Clinics of North America, 1996
Evidence from multiple sources indicates that SSc does not occur randomly in the population; there are particular groups who are at greater risk. The overall incidence rate of SSc in the adult population of the United States is approximately 20 per million per year; this rate has increased from 1944 to 1973, but has been relatively stable since that ...
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Evidence from multiple sources indicates that SSc does not occur randomly in the population; there are particular groups who are at greater risk. The overall incidence rate of SSc in the adult population of the United States is approximately 20 per million per year; this rate has increased from 1944 to 1973, but has been relatively stable since that ...
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Clinics in Dermatology, 1994
S cleroderma in childhood is rare. It affects all races and can begin at any age, with boys being affected almost as frequently as girls.’ Classification and course are even more diflicult to determine than in the adult disease; the condition is predominantly confined to the skin and underlying tissues as either morphea or linear scleroderma, which ...
B M, Ansell, F, Falcini, P, Woo
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S cleroderma in childhood is rare. It affects all races and can begin at any age, with boys being affected almost as frequently as girls.’ Classification and course are even more diflicult to determine than in the adult disease; the condition is predominantly confined to the skin and underlying tissues as either morphea or linear scleroderma, which ...
B M, Ansell, F, Falcini, P, Woo
openaire +2 more sources