全身性硬皮病1例，中年妇女

Clinical complementary medicine and pharmacology Pub Date : 2023-05-15 DOI:10.12737/2409-3750-2023-9-1-22-26

M. Demin, O. Avdeeva

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引用次数: 0

摘要

系统性硬皮病是一种罕见的慢性疾病，以皮肤、血管、关节和内脏器官的弥漫性纤维化和病理改变为特征。本文报告1例全身性硬皮病患者的临床病例，其皮肤和血管病变表现明显，如硬化、面部遮盖、“钱袋嘴”、雷诺综合征，同时伴有关节、肌肉病变、免疫功能紊乱，并发类固醇骨质疏松多发骨折

本文章由计算机程序翻译，如有差异，请以英文原文为准。

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CLINICAL CASE SYSTEMIC SCLERODERMA A MIDDLE-AGED WOMAN

Systemic scleroderma is a rare chronic disease characterized by the development of diffuse fibrosis, pathological changes in the skin, blood vessels, joints and internal organs. The article presents a clinical case of a patient with systemic scleroderma with such obvious manifestations of skin and vascular lesions as sclerodactyly, masking of the face, "purse-string mouth", Raynaud's syndrome, as well as lesions of the joints, muscles, immunological disorders, the development of steroid osteoporosis with multiple fractures

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来源期刊

Clinical complementary medicine and pharmacology Complementary and Alternative Medicine

自引率

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审稿时长

67 days