期刊文献+

原发性和继发性干燥综合征患者的临床及实验室特征分析 被引量:2

Analysis of the clinical and laboratory characteristics in patients with primary and secondary Sjogren′s syndrome
原文传递
导出
摘要 目的:观察原发性和继发性干燥综合征(SS)患者的不同特点,为临床诊断SS提供新的信息。方法:选取原发性SS(pSS)患者44例,继发性SS(sSS)患者37例,其中17例继发于系统性红斑狼疮(SS-SLE),20例继发于类风湿关节炎(SS-RA)。比较pSS和sSS临床特征和实验室结果的不同特点。结果:1)pSS、SS-SLE和SS-RA发病年龄分别为(45.3±11.7)岁,(42.9±11.7)岁和(53.2±13.8)岁。2)pSS发热、唇腺活检、抗SSA和抗SSB阳性率明显高于SS-RA,猖獗齿阳性率明显高于SS-SLE(P均<0.05)。SS-SLE组蛋白尿发生率较pSS多见(P=0.000),肾小管酸中毒有增多趋势(P=0.06)。SS-RA组关节痛发生率较pSS多见。pSS腮腺肿痛较sSS明显多见(P=0.003),周围神经病变的发生率较sSS少见(P=0.044)。3)pSS血红蛋白(HGB)降低的发生率比sSS明显少见(P=0.045),且SS-SLE白细胞(WBC)、血K+和补体C3降低比pSS明显增多,SS-RA类风湿因子(RF)和C反应蛋白(CRP)增高比pSS多见。4)pSS和sSS的ANA核型以颗粒型最常见,此外pSS核仁型、核膜型,sSS均质型和胞浆型相对较多见。结论:pSS与sSS比较,起病比SS-RA早,临床特征典型,腮腺肿痛明显,出现蛋白尿、贫血、C3降低及周围神经病变较少,ANA核型以颗粒型、核仁型、核膜型多见。 Objective: To investigate the different characteristics in patients with primary and secondary Sjogren's syndrome(SS), in order to provide new information for diagnosis of SS. Methods: 44 primary Sjogren's syndrome(pSS) and 37 secondary Sjogren's Syndrome(sSS) patients were enrolled ( 17 patients secondary to SLE, SS-SLE and 20 patients secondary to RA, SS-RA ). The different clinical features and laboratory examination in patients with pSS and sSS were compared. Results: The mean age at onset was (45.3 ± 11. 7)ys in pSS and was (42.9 ± 11. 7)ys in SS-SLE and was (53.2 ± 13.8)ys in SS-RA respectively, pSS patients were younger than those with SS-RA (P = 0.02). We found higher percentage of fever, labial gland biopsy and anti-SS-A/B antibodies in pSS patients than those with SS-RA and higher percentage of dental necrosis than those with SS-SLE (P 〈 0.05). More proteinuria and renal tubule acidosis were found in SS-SLE patients than those in pSS (P = 0.000, P = 0.06). More arthralgia was found in SS-RA patients than those with pSS. More parotid gland enlargement was found in pSS patients than in the sSS ones ( P = 0. 003 ). PSS presented a lower prevalence of peripheral neuropathy and hemoglo- bin than sSS patients (P = 0.044, 0.045 ). The frequency of the decreasing of white blood cell, serum K and C3 in SS-SLE and rheumatoid factor and c-reactive protein in SS-RA patients were higher than those of pSS. The granular pattern of ANA was the most common pattern in pSS and sSS. Besides, nucleolar pattern and nuclear membrane pattern were more often in pSS cases, and homogeneous pattern and kytoplasm pattern were more often in sSS. Conclusion: Compared with patients with pSS and sSS, the pSS patients were younger than SS-RA ones in disease onset and clinical features tend to be more typical. PSS patients may have more common parotid gland enlargement and present less frequently to have proteinuria, anaemia, C3 decreasing and peripheral neuropathy. More nucleolar pattern and nuclear membrane pattern were found in pSS.
出处 《军医进修学院学报》 CAS 北大核心 2008年第5期371-373,共3页 Academic Journal of Pla Postgraduate Medical School
关键词 干燥综合征 红斑狼疮 系统性 关节炎 类风湿 Sjogren's syndrome lupus erythematosus, systemic arthritis rheumatoid
  • 相关文献

参考文献8

  • 1Vitali C, Bombardieri S, Jonsson R, et al. Classification criteria for Sjogren's syndrome: a revised version of the European critera proposed by the American-European Consensus Group [ J ]. Ann Rheum Dis, 2002, 61:554.
  • 2Bernacchi E, Amato L, Parodi A. Sjogren's syndrome: a retrospective review of the cutaneous features of 93 patients by the halian Group of Immunodermatology[J].Clin Exp Rheumatol, 2004, 22(1) :55-62.
  • 3De Vita S, Lorenzon G, Rossi G, et al. Salivary gland echography in primary and seccndary Sj gren's Syndrome[ J]. Clin Exp Rheu- matol, 1992, 10:351-356.
  • 4Rosenbaum R. Neuromuscular complications of connective tissue diseases[J]. Muscle Nerve, 2001, 24(2):154-169.
  • 5Nadkar MY, Agarwal R, Samant RS, et al. Neuropathy in rheumatoid arthritis [ J]. J Assoc Physicians India, 2001, 49: 217- 220.
  • 6Shoshtary J, Adib M. Peripheral neuropathy in systemic lupus erythematosus in Southern Iran[ J ]. Electromyogr Clin Neurophysiol, 2005, 45(3) :145-148.
  • 7Ramos-Casals M, Brito-Zeron P, Yague J, et al. Hypocomplementaemia as an immunological marker of morbidity and mortality in patients with primary Sjogren's syndrome [ J ]. Rheumatology ( Oxford), 2005, 44( 1 ) :89-94.
  • 8Pillemer SR, Casciola-Rosen L, Baum B J, et al. Centromere protein C is a target of autoantibodies in Sj gren's syndrome and is uniformly associated with antibodies to Ro and La [ J ]. J Rheumatol, 2004, 31(6):1121-1125.

同被引文献52

  • 1施孝文.针灸治疑难病3则[J].中国针灸,2002,22(S1):16-17. 被引量:1
  • 2程建中.中医“久病必瘀”的机理探讨及临床应用体会[J].中医药研究,1996,12(2):6-8. 被引量:12
  • 3佟胜全,吴庆军,张奉春,曾小峰.原发性胆汁性肝硬化合并肾小管酸中毒一例[J].中华内科杂志,2005,44(12):897-897. 被引量:1
  • 4陈灏珠,林果为,王吉耀实用内科学[M].14版北京:人民卫生出版社:2013:9.
  • 5Van Den Wildenberg M J, Hoorn E J, Mohebbi N, et al. Distal renal tubular acidosis with multiorgan autoimmunity : a case report [ J ] . Am J Kidney Dis, 2015, 65 ( 4 ) : 607-610.
  • 6lto N, Ihara K, Kamoda T, et al. Antosomal dominant distal renal tubular acidosis caused by a mutation in the anion exchanger 1 gene in a Japanese family [ J ] . CEN Case Reports, 2015, g ( 2 ) : 218-222.
  • 7Hamnvik 0-, Vaidya A, Becker C. Wasting away [ J ] . N Engl J Med, 2014, 370 ( 7 ) : 959-966.
  • 8Chen YM, Hsieh TY, Chen DY, et al. Bilateral nephrocalcinosis, distal renal tubular acidosis and interstitial nephritis in primary SjSgren' s syndrome [ J ] . Joint Bone Spine, 2014, 81 ( 6 ) : 542.
  • 9Sharma S, Gupta A, Saxena S. Comprehensive clinical approach to renal tubular acidosis [ J ] . Clin Exp Nephrol, 2015, 19 ( 4 ) : 556- 561.
  • 10Basu G, Sudhakar G, Mohapatra A. Renal tubular acidosis [ J ] . Clinical Queries : Nephrology, 2013, 2 ( 4 ) : 166-178.

引证文献2

二级引证文献17

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部