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Scleroderma is a rare autoimmune condition of uncertain etiology that affects approximately 1 in 40,000 people in the United States and is characterized by excessive collagen deposition in all organ systems including the skin [1]. Common symptoms of scleroderma include Calcinosis, Raynaud phenomenon, Esophageal dysmotility, Sclerodactyly, and Telangiectasia (CREST syndrome) as well as vascular, pulmonary and cardiac pathology [2]. Symptoms are often debilitating and lead to functional and aesthetic compromise. Plastic surgical intervention may be a viable option for a subset of patients to ameliorate functional and / or aesthetic symptomatology depending on the subtype of scleroderma, the magnitude of disease extension and the operative setting.
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Brooks et al. (2018) studied this question.
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