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xi tong xing ying pi bing de zhong xi yi jie he hu li
Author(s): 
Pages: 1090-1092
Year: Issue:  7
Journal: Hebei Journal of Traditional Chinese Medicine

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Abstract: 系统性硬皮病(systemicsclerosis,SSc)是一种以皮肤及内脏各系统胶原纤维化为特征的结缔组织疾病,其病因不明,病理机制涉及免疫、血管、胶原代谢及遗传等方面异常,为临床难治少见疾病.近似中医学文献中的“皮痹”.主要皮肤表现为局限性或弥漫性的皮肤发硬、光滑,呈象牙色,无法移动,分为局限型和系统型,其中SSc除影响皮肤外还可影响心、肺、肾和消化道等器官,预后不良[1].SSc的治疗以全身用药为主,以求改善某些脏器的功能,延长生命,促进康复,而对患者进行有效的护理对治疗和预后也有很大的影响.兹将SSc的中西医结合护理体会如下.
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