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伴有凹陷性水肿的缓解性血清阴性对称性滑膜炎的临床谱。加泰罗尼亚RS3PE研究小组。

The clinical spectrum of remitting seronegative symmetrical synovitis with pitting edema. The Catalán Group for the Study of RS3PE.

作者信息

Olivé A, del Blanco J, Pons M, Vaquero M, Tena X

机构信息

Rheumatology Section, Hospital Universitari Germans Trias i Pujol, Spain.

出版信息

J Rheumatol. 1997 Feb;24(2):333-6.

PMID:9034993
Abstract

OBJECTIVE

To describe the clinical and laboratory features and outcome of patients with remitting seronegative symmetrical synovitis with pitting edema (RS3PE).

METHODS

A retrospective multicenter study of patients with RS3PE fulfilling the following criteria: (1) bilateral pitting edema of both hands, (2) sudden onset of polyarthritis, (3) age > 50 years, (4) seronegative for rheumatoid factor (RF).

RESULTS

27 patients with RS3PE were included, mean age 71.7 years (58-92), 18 men (66.6%) and 9 women (33.3%). Relevant history was noted in 2 patients with polymyalgia rheumatica. Main clinical features were polyarthritis and edema of both hands. Polyarthritis involved metacarpophalangeal joints in 22 patients (81.5%), proximal interphalangeal joints in 19 (70.4%), wrists in 15 (55.5%), shoulders in 13 (48%), elbows in 3 (11.1%), knees in 9 (33.3%), and ankles in 7 (25.9%). All patients were RF negative. Antinuclear antibodies were positive at low titer in 8 patients. Erosions were present in one patient. Two patients developed T lymphoma and one myelodysplastic syndrome.

CONCLUSION

RS3PE is a heterogeneous syndrome the clinical history, presence of erosions, and evolution to hematological diseases in our patients suggest that RS3PE may not be a distinct clinical entity.

摘要

目的

描述缓解型血清阴性对称性滑膜炎伴凹陷性水肿(RS3PE)患者的临床、实验室特征及预后。

方法

对符合以下标准的RS3PE患者进行一项回顾性多中心研究:(1)双手双侧凹陷性水肿;(2)多关节炎突然起病;(3)年龄>50岁;(4)类风湿因子(RF)血清阴性。

结果

纳入27例RS3PE患者,平均年龄71.7岁(58 - 92岁),男性18例(66.6%),女性9例(33.3%)。2例患者有风湿性多肌痛相关病史。主要临床特征为多关节炎和双手水肿。多关节炎累及掌指关节22例(81.5%)、近端指间关节19例(70.4%)、腕关节15例(55.5%)、肩关节13例(48%)、肘关节3例(11.1%)、膝关节9例(33.3%)、踝关节7例(25.9%)。所有患者RF均为阴性。8例患者抗核抗体低滴度阳性。1例患者出现侵蚀性病变。2例患者发生T淋巴瘤,1例发生骨髓增生异常综合征。

结论

RS3PE是一种异质性综合征,我们患者的临床病史、侵蚀性病变的存在以及向血液系统疾病的演变提示RS3PE可能不是一个独特的临床实体。

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