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缓解性血清阴性对称性滑膜炎伴凹陷性水肿。RS3PE综合征。

Remitting seronegative symmetrical synovitis with pitting edema. RS3PE syndrome.

作者信息

McCarty D J, O'Duffy J D, Pearson L, Hunter J B

出版信息

JAMA. 1985 Nov 15;254(19):2763-7.

PMID:4057484
Abstract

Eight elderly men and two elderly women presented with symmetrical polysynovitis of acute onset involving most of their appendicular joints and flexor digitorum tendons associated with pitting edema of the dorsum of both hands and both feet. Onset of seven of the ten cases could be pinpointed almost to the hour. Rheumatoid factors were absent from serum samples in all, and no radiologically evident erosions developed. Clinical and laboratory signs of inflammation and the edema disappeared gradually in each case. Treatment consisted of aspirin or other nonsteroidal anti-inflammatory drugs. Hydroxychloroquine, 200 to 400 mg/day, was given in six and gold therapy in two cases. Painless limitation of motion of the wrists and/or fingers persisted in all, although the patients were both unaware of and unhampered by this abnormality. Six of eight cases where typing was possible were positive for HLA-B7, CW7, and DQW2 (relative risk for B7, 9.5). Three cases of this syndrome were found in a consecutive series of 52 men diagnosed as having definite "rheumatoid arthritis," and thus represent a distinctive condition with an excellent prognosis.

摘要

八名老年男性和两名老年女性出现急性起病的对称性多滑膜炎,累及大部分四肢关节和指屈肌腱,伴有双手和双足背部凹陷性水肿。十例中有七例的起病时间几乎可以精确到小时。所有血清样本中均无类风湿因子,且未出现放射学上明显的侵蚀。炎症的临床和实验室体征以及水肿在每个病例中逐渐消失。治疗包括使用阿司匹林或其他非甾体抗炎药。六例给予羟氯喹,每日200至400毫克,两例采用金制剂治疗。尽管患者既未意识到也未受此异常影响,但所有人的手腕和/或手指均存在无痛性活动受限。在八例可行分型的病例中,六例HLA - B7、CW7和DQW2呈阳性(B7的相对风险为9.5)。在连续诊断为明确“类风湿关节炎”的52名男性中发现了三例该综合征病例,因此这是一种预后良好的独特病症。

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