摘要
系统性硬皮病是一种自身免疫性结缔组织病,该病以出现微血管损伤及自身免疫系统的异常为特征,导致皮肤增厚和内脏器官的纤维化,并伴随有自身抗体的出现。这些自身抗体与不同的临床表型紧密相关,对疾病的病因、诊断、治疗及预后提供了很大帮助。
出处
《国际检验医学杂志》
CAS
2006年第8期688-690,共3页
International Journal of Laboratory Medicine
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