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荨麻疹性血管炎 被引量:2

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摘要 慢性或复发性荨麻疹性损害在临床较为常见 ,多被诊断为慢性特发性荨麻疹 ,其中 30 %患者是由IgG型抗IgE受体或IgE自身抗体所致 ,只有少数 (约 10 % )患者可诊断为荨麻疹性血管炎 ,此病还可作为其他疾病的表现之一 ,诸如系统性红斑狼疮、低补体血症性荨麻疹性血管炎综合征、干燥综合征及混合性冷球蛋白血症等。本文就荨麻疹性血管炎的临床。
作者 陈红清
出处 《国外医学(皮肤性病学分册)》 2001年第4期238-240,共3页 Foreign Medical Sciences(Section of Dermatology and Venereology)
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参考文献3

  • 1Wisnieski JJ. Urticarial vasculitis. Curr Opin Rheunatol, 2000, 12( 1 ) :24-31.
  • 2Davis MD, Daoud MS, Kirby B, et al. Clinicopathologic correlation of hypocomplementemic and normocomplementemic urticarial vasculitis. J Am Acad Dermatol, 1998,38(6Pt1) :899-905.
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同被引文献22

  • 1李敬扬,周炜,张卓莉,董怡.101例原发性干燥综合征临床首发症状及误诊分析[J].中级医刊,2004,39(11):19-21. 被引量:35
  • 2吕静,李惠,单葵.红斑狼疮和扁平苔藓重叠综合征1例[J].临床皮肤科杂志,2007,36(6):397-397. 被引量:4
  • 3Wisnieskj JJ. Urticarial vasculitis[J]. Curr Opin Rheumatol, 2000, 12(1): 24-31.
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  • 7Bielsa I, Carrascosa JM, Hausmann G, et al. An immunohistopathologic study in cutaneous necrotizing vasculitis [ J]. J Cutan Pathol, 2000, 27:130-135.
  • 8Bernacchi E, Amato L, syndrome : aretrospective features of 93 patients Immunodermatology [ J]. Parodi A, et al. Sjtigren ' s review of the cutaneous by the Italian Group of Clin Exp Rheumatol, 2004,22:55-62.
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