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首页> 外文期刊>The Journal of foot and ankle surgery: official publication of the American College of Foot and Ankle Surgeons >Remitting seronegative symmetrical synovitis with pitting edema (RS3PE) syndrome: a review of the literature and a report of three cases.
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Remitting seronegative symmetrical synovitis with pitting edema (RS3PE) syndrome: a review of the literature and a report of three cases.

机译:伴有点蚀性水肿(RS3PE)综合征的缓发性血清阴性对称性滑膜炎:文献复习并报告3例。

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摘要

Remitting seronegative symmetrical synovitis with pitting edema (RS3PE) syndrome is a disease that commonly produces symmetrical synovitis and swelling of both the upper and lower extremities. It generally involves the wrists, hands, feet, and ankles of the affected individual. This syndrome most often resembles that of polymyalgia rheumatica and rheumatoid arthritis and usually affects elderly Caucasian males. Serological testing is typically negative except for a mild to moderate elevation of the erythrocyte sedimentation rate. The HLA-B7 phenotype is present in approximately 50% of patients with this syndrome. Treatment of RS3PE syndrome is heralded by the predictable response to low-dose corticosteroid or hydroxychloroquine therapy. There has been no previous mention of this condition in the podiatric literature. Presented below is a review of this syndrome and three case studies.
机译:患有点状水肿(RS3PE)综合征的缓发性血清阴性对称性滑膜炎是一种通常会产生对称性滑膜炎和上,下肢肿胀的疾病。它通常涉及受影响个体的手腕,手,脚和脚踝。该综合征最常与风湿性多肌痛和类风湿性关节炎类似,通常会影响老年白种人。血清学检查通常是阴性的,只是红细胞沉降率有轻度到中度升高。 HLA-B7表型存在于大约50%的患有这种综合征的患者中。对低剂量皮质类固醇或羟氯喹治疗的可预测反应预示着RS3PE综合征的治疗。儿科文献中以前没有提到这种情况。下面介绍的是对该综合征的回顾和三个案例研究。

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