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作 者:Comlan Albert Dovonou Cossi Adébayo Alassani Séraphin Ahoui Lauren Gueguen Arthur Capdeville Elie Cornec-Le Gall Laurent Doucet Yannick Le Meur
机构地区:[1]Borgou Regional University Teaching Hospital, Parakou, Benin [2]Regional University Teaching Hospital of Brest-La Cavale Blanche, Brest, France
出 处:《Open Journal of Rheumatology and Autoimmune Diseases》2017年第3期158-166,共9页风湿病与自身免疫疾病期刊(英文)
摘 要:Systemic scleroderma is a rare disease in which visceral manifestations occur, particularly peripheral vascular, digestive, cardiopulmonary and renal. It is pathology with a predilection for women. The present clinical case is that of a man with the renal complications of scleroderma and the difficulties of the treatment even in the developed countries like France. In the present case, the management of this disease required a high dose of corticosteroid therapy and extra-renal purification. Early detection of complications through a minimal clinical examination supplemented with paraclinic tests has proved necessary.Systemic scleroderma is a rare disease in which visceral manifestations occur, particularly peripheral vascular, digestive, cardiopulmonary and renal. It is pathology with a predilection for women. The present clinical case is that of a man with the renal complications of scleroderma and the difficulties of the treatment even in the developed countries like France. In the present case, the management of this disease required a high dose of corticosteroid therapy and extra-renal purification. Early detection of complications through a minimal clinical examination supplemented with paraclinic tests has proved necessary.
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