Gatter R A, Richmond J D
J Rheumatol. 1975 Sep;2(3):340-5.
Evaluation of 158 synovial fluids, mainly from patients with rheumatoid arthritis (RA) and the crystal deposition fiseases (CDD), revealed differences in the differential white blood count and numbers of cytoplasmic inclusion bodies (CIB) present. Lymphocytes and CIB were increased in RA, suggesting a different pathologic mechanism from that of CDD. Lymphocyte-like cells contained CIB implying phagocytic capability. Lymphocytes were the initial predominant cell type in RA of less than six weeks disease duration. Later polymorphonuclear leukocytes increased, possibily representing a secondary non-specific inflammatory response similar to that seen in CDD.
对158份主要来自类风湿性关节炎(RA)患者和晶体沉积疾病(CDD)患者的滑液进行评估后发现,其白细胞分类计数和细胞质包涵体(CIB)数量存在差异。RA患者的淋巴细胞和CIB增加,提示其病理机制与CDD不同。淋巴细胞样细胞含有CIB,这意味着它们具有吞噬能力。在病程少于六周的RA患者中,淋巴细胞是最初的主要细胞类型。后来多形核白细胞增加,这可能代表了一种类似于CDD中所见的继发性非特异性炎症反应。