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白塞病55例临床分析 被引量:2

Clinical Analysis of 55 Cases of Behcet's Disease
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摘要 目的分析白塞病的临床特征,减少临床医生的误诊率和漏诊率。方法对2008年1月-2013年7月本院口腔科和皮肤科确诊的55例白塞病患者临床资料进行回顾性分析。结果男∶女为1.29∶1;平均发病年龄(31.22±11.37)岁;平均病程(2.50±1.86)年。最常见的临床表现为口腔溃疡(98.18%),其次为生殖器溃疡(70.91%)、针刺反应阳性(69.09%)、发热(38.18%)、关节炎(36.36%)、结节性红斑(34.55%)、假性毛囊炎(30.91%)和眼损害(29.09%)。实验室检查异常包括血沉增快(56.36%),白细胞计数升高(38.18%),IgG升高(36.36%),C反应蛋白升高(32.73%),中性粒细胞百分比升高(27.27%),IgM升高(20.00%)。结论白塞病的临床表现多样,可累及多器官和多系统,其实验室检查结果和组织病理学表现缺乏特异性,诊断主要依靠临床表现。 Objective To study the clinical features of Behcet's disease in order to minimize the misdiagnosis and missed diagnosis rates. Methods The clinical data of 55 cases of Behcet's disease from department of stomatology and dermatology of our hospital from January 2008 to July 2013 were retrospectively analyzed. Results The ratios of male/female weere 1.29: 1. The average age at onset of Behcet's disease was 31.22 ± 11.37 years. The mean duration was 2.50 ± 1.86 years. The most common clinical manifestation was oral aphthosis ( 98.18 % ), followed by genital aphthosis ( 70.91% ), positive patbergy test (69. 09% ), fever (38.18%) ,arthritis(36. 36% ), erythema nodosum(34. 55% ) ,pseudofolliculitis (30. 91% ) and ophthalmologic lesions (29.09%). laboratory abnormalities included an elevated erythrocyte sedimentation rate(56. 36% ) ,leukocytosis (38. 18% ), an elevated IgG level (36.36%), an elevated C reactive protein level ( 32.73% ), neutrophilia(27.27% )and an elevated IgM level(20. 00% ). Condusion Multiple organs and systems could be involved in Behcet's disease with diversity of clinical manifestations. There were no specific laboratory and histopathology findings and Behcet's disease should be diagnosed mainly by clinical manifestations.
出处 《中国皮肤性病学杂志》 CAS 北大核心 2014年第6期579-580,共2页 The Chinese Journal of Dermatovenereology
关键词 白塞病 临床分析 Behcet's disease Clinical research
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参考文献6

  • 1Davatehi F,Shahram F,Chams-Davatehi C,et al.Beheet's disease:from east to west[J].Clin Reumatol,2010,29(6):823-833.
  • 2Reynold N.Vasculitis in Behcet's syndrome:evidence-based review[J].Curr Opin Reumatol,2008,20(2):347-352.
  • 3樊超,黄巍,李芃,涂亚庭.白塞病78例临床分析[J].中国皮肤性病学杂志,2007,21(11):673-675. 被引量:5
  • 4李文政,惠艳.白塞病38例临床分析[J].中国皮肤性病学杂志,2004,18(10):602-603. 被引量:2
  • 5杨怀珠,赵燕云.白塞病28例临床分析[J].中国皮肤性病学杂志,2004,18(9):549-550. 被引量:4
  • 6Davatchi F,Sadeghi Abdollahi B,Shahram F,et al.Validation of the International Criteria for Behcet's Disease(ICBD)in Iran [J].Int J Rheum Dis,2010,13(1):55-60.

二级参考文献19

  • 1陈灏珠.实用内科学[M](第10版)[M].北京:人民卫生出版社,1998.2076-2077.
  • 2赵辨.临床皮肤病学[M](第2版)[M].南京:江苏科技出版社,1996.113.
  • 3赵辨.临床皮肤科学[M](第3版)[M].南京:江苏科学技术出版社,2001.423.
  • 4蒋明 朱立平 林孝义 主编.风湿病学[M].北京:科学出版社,1998.1031-1032.
  • 5Ghate JV,Jorizzo JL.Behcet's disease and complek qphthosis[J].J Am Acad Dermatol,1999,40(1):1-12.
  • 6International Study Group for Behcet's Disease. Criteria for diagnosis of Behcet's disease[J].Lancet,1990,335(8697):1078-1080.
  • 7Alpsoy ER,Durusoy CI,Yilmaz ER,et al.Interferon alfa-2a in the treatment of Behcet disease: a randomized placebo-controlled and double-blind study[J].Arch Dermatol,2002,138:467-471.
  • 8Vencovsky J,Paleckova A,Becvar R,et al. Antineutrophil cytoplastic antibodies-ANCA[J].Cas-Lek-Cesk,1992,131:577-581.
  • 9Revised Japanese criteria for Behcet' s disease. Behcet' s disease research committee of Japan 1987 congress news of the 6th SEAPAL congress of rheumatology, 1988.
  • 10Kone-Paut I, Yurdakul S, Bahabri SA, et al. Clinical features of Behcet' s disease in children: an international collaborative study of 86 eases [J]. J Pediatr,1998,132(4) :721 -725.

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