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According to the American Arthritis Foundation£¬ write ¡°Summary of rheumatic diseases£¬¡° 9th Edition provides diagnostic criteria for systemic scleroderma£¬ those who meet
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£¨A£© localized scleroderma need to identify the following diseases:
1£¬. spot early damage for sizes shrink£¬ or bluish skin color was£¬ dimpled
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Raynaud¡®s phenomenon is often due to an early manifestation of systemic sclerosis£¬ and may appear alone for many years£¬ so there should be Raynaud¡®s phenomenon of systemic
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£¨1£© anti-nuclear antibody: positive£¬ with speckled pattern£¬ nucleolar type based. £¨2£© anti-Scl-70 antibody: positive£¬ is diffuse SSc labeled antibody.
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Scleroderma many believe that genetic£¬ infectious£¬ immune regulation disorders£¬ connective tissue metabolism and vascular abnormalities related. Localized no damage
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Systemic sclerosis can affect multiple body systems£¬ causing the corresponding system lesions£¬ Ruoyi organ dysfunction occurs£¬ the treatment and prognosis is poor£¬
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Scleroderma process is slow£¬ and sometimes obvious symptoms may be diagnosed several years after. But one thing worth noting is that the patient will usually appear
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Morphea is a type of localized scleroderma. According to their shape and scope of different lesions can be divided into porphyritic morphea£¬ droplet morphea
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Localized scleroderma change can be diagnosed based on typical skin.
System sclerosis: American College of Rheumatology £¨ARA£© 1998
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Systemic scleroderma is easy with dermatomyositis£¬ scleroderma adult confusion£¬ attention should be identified. £¨A£© the acute phase of dermatomyositis have eye puffiness
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£¨A£© localized scleroderma need to identify with these various diseases.
1 spot early damage for sizes shrink£¬ or bluish skin color was£¬
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