calcinosis cutis oor Spaans

calcinosis cutis

naamwoord
en
a group of disorders wherein calcium deposits form in the skin

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calcinosis cutánea

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This form of systemic scleroderma is usually less severe than other forms, consisting of calcinosis cutis, Raynaud's phenomenon, esophageal dysfunction, sclerodactyly, and telangiectasis.
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* May - June 2010 Calcinosis cutis in a patient with systemic lupus erythematosus
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Calcinosis cutis in a patient with systemic lupus erythematosus | Reumatología Clínica (English Edition)
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To propose a new classification of the calcinosis cutis.
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Calcinosis Cutis (26)Progressive Systemic Scleroderma (51)
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DermIS - Calcinosis Cutis Mixed Connective Tissue Disease (image)
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Calcinosis cutis (CC) is defined as the deposition of calcium salts in the skin.
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Calcinosis Cutis, Mixed Connective Tissue Disease
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Systemic corticosteroids have caused deposition of calcium in the skin (calcinosis cutis).
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The latter form is termed limited cutaneous scleroderma or CREST syndrome (calcinosis cutis, Raynaud phenomenon, esophageal dysmotility, sclerodactyly, telangiectasias).
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Without intensive early treatment, complications such as calcinosis cutis and lipodystrophy can develop in the chronic phases of the disease. Early recognition is therefore key to management.
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Calcinosis cutis is a disease caused by accumulation and deposition of calcium salts in the tissue, which can result in serious injuries, whose therapeutic approach is not clearly established: it is restricted to symptomatic treatment or intravenous sodium thiosulfate in the most severe cases, but its administration carries some risks and is particularly difficult in pediatric patients.
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Conclusions: a) clinicopathologic differences allow to distinguish two groups of patients: in one of them CVC represents an epiphenomenon of different dermatoses of known diagnosis, and in the other it is associated with renal failure; b) the mechanisms by which CVC is caused is probably multifactorial, and c) we propose a new classification of the calcinosis cutis that includes vascular and extravascular forms (with three subtypes: dystrophic,
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Conclusions: a) clinicopathologic differences allow to distinguish two groups of patients: in one of them CVC represents an epiphenomenon of different dermatoses of known diagnosis, and in the other it is associated with renal failure; b) the mechanisms by which CVC is caused is probably multifactorial, and c) we propose a new classification of the calcinosis cutis that includes vascular and extravascular forms (with three subtypes: dystrophic, metastatic and idiopathic).
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