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13 Ιουλ 2023 · Prognosis . CREST syndrome is associated with a lower survival rate than other types of systemic sclerosis, like sine scleroderma.
5 Απρ 2024 · Introduction. Systemic sclerosis, also known as scleroderma, is a rare connective tissue disorder with an unknown and complex pathogenesis. Scleroderma can be divided into 2 primary forms—localized scleroderma (including morphea, linear scleroderma, and scleroderma en coup de sabre) and systemic sclerosis.
9 Ιουν 2022 · CREST syndrome is a clinical entity associated with systemic sclerosis, which meets at least three of the five clinical features: calcinosis, Raynaud’s phenomenon, esophageal dysmotility, sclerodactyly, and telangiectasia.
5 Οκτ 2020 · Pathophysiology. Three primary pathologic features are found in scleroderma and include increased collagen deposition, perivascular mononuclear cell infiltration, and vascular abnormalities. The...
29 Σεπ 2023 · Limited sclerosis (CREST syndrome) Healthcare providers usually refer to limited scleroderma with the acronym CREST syndrome. Each letter in CREST stands for a symptom it causes: Calcinosis (extra calcium deposits in your skin). Raynaud’s syndrome (color changes and numbness in your fingertips and toes).
Introduction. Scleroderma is a heterogeneous chronic connective tissue disease that can be either localized (localized scleroderma, LoS) or systemic (SSc) involving the skin and internal organs and characterized by aberrant immune responses, vascular damage, and excessive collagen deposition and fibrosis [ 1 ].
18 Απρ 2023 · Risk factors for and possible causes of systemic sclerosis (scleroderma) Society guideline links: Systemic sclerosis (scleroderma) Systemic sclerosis (scleroderma) and pregnancy; Treatment and prognosis of interstitial lung disease in systemic sclerosis (scleroderma) Undifferentiated systemic rheumatic (connective tissue) disease and overlap ...
