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皮肤血管炎163例组织病理及临床分析 被引量:6

Histopathological and clinical analysis of 163 cases of cutaneouos vasculitis
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摘要 目的:总结163例皮肤血管炎组织病理和临床特点,指导临床诊疗。方法:采用回顾分析的方法对163例皮肤血管炎患者的皮损组织病理及临床资料作分析总结。结果:163例患者中男64例,女99例,平均年龄39.8岁,平均病程3.68年。与发病有关因素依次为:感染15.9%,系统性免疫性疾病15.9%,季节性因素8.59%,药物3.68%,食物1.84%,劳累0.6%;不明原因52.7%。组织病理分为5型,其中白细胞碎裂性血管炎36.8%,淋巴细胞性血管炎10.43%,节段透明性血管炎1.84%,肉芽肿性血管炎8.59%,血管炎伴脂膜炎[42.3%(69例),其中57例(82.6%)为白细胞碎裂性血管炎]。部分临床表现与组织病理特点有很好的一致性,但时有相左。结论:皮肤血管炎分类复杂,临床表现各异,根据组织病理学特点分型更加准确。白细胞碎裂性血管炎最常见,加上伴脂膜炎的白细胞碎裂性血管炎总共占71.7%,其中有部分临床损害类似脂膜炎,此时需要组织病理检查确诊。组织病理学分型对皮肤血管炎的治疗有指导作用。 Objective: To improve the diagnosis and treatment of cutaneous vasculitis through analyzing the clinical and pathological characteristics of 163 cases, Method: The clinical and pathological data of 163 patients with cutaneous vasculitis were retrospectively analyzed. Results: There were 64 male and 99 female patients, with an average age of 39.8 years and the disease-course of 3.68 years on average. The associated predisposing factors were infection (15.9%), systemic immunological diseases (15.9%), seasonal factor (8.59%), medicines (3.68%), food (1.84%) and tiredness (0.6%). The cause of more than half (52.7%) of the patients was unknown. Histopathology of skin specimens could be divided into 5 types: leukocytoclastic vasculitis (60 cases, accounting for 36.8%), lymphocytic vasculitis (17, 10.43%), granulomatous vasculitis (14, 8.59%), segmental hyalinizing vasculitis (3, 1.84%), and vasculitis complicated with panniculitis (69, 42.3%), fifty-seven patients of the latter (82.6%) were leukoeytoclasitic vasculitis. The clinical manifestations were consistent with the pathological features in some but not with all the cases. Conclusion: Leukocytoclastic vasculitis is most common in these cases, accounting for 71.7%, some were accompanied by panniculitis and mimicked pannieulitis clinically. The histopathological examination is needed in this situation for the final diagnosis and proper treatment.
出处 《临床皮肤科杂志》 CAS CSCD 北大核心 2009年第7期418-422,共5页 Journal of Clinical Dermatology
关键词 皮肤血管炎 组织病理学 分析 临床 cutaneous vaseulitis histopathology analysis, clinic
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参考文献7

  • 1Fiorentino DF.Cutaneous vasculitis[J].J Am Acad Dermatol,2003,48(3):311-340.
  • 2张凡,涂平,朱学骏.青斑样血管炎[J].临床皮肤科杂志,2007,36(12):803-804. 被引量:15
  • 3Mascaró JM Jr,Baselga E.Erythema induratum of Bazin[J].Dermatol Clin,2008,26(4):439-445.
  • 4Melikoglu M,Kural-Seyahi E,Tascilar K,et al.The unique features of vasculitis in Behcet's syndrome[J].Clin Rev Allergy Immunol,2008,35(1-2):40-46.
  • 5左付国,赵天恩,卢宪梅.皮肤血管炎的免疫学及分子生物学研究进展[J].国外医学(皮肤性病学分册),2003,29(4):234-237. 被引量:8
  • 6Csernok E,Gross WL.Primary vasculitides and vasculitis confined to skin:clinical features and new pathogenic aspects[J].Arch Dermatol Res,2000,292(9):427-436.
  • 7左付国.皮肤血管炎的某些研究进展[J].中国麻风皮肤病杂志,2003,19(2):143-144. 被引量:8

二级参考文献41

  • 1赵文,李连宏,夏玉坤,宋临秋.11例青斑血管炎患者皮损免疫组织化学分析[J].中华皮肤科杂志,2005,38(10):645-645. 被引量:8
  • 2冯素英,靳培英.20例青斑血管炎患者的临床特点和治疗分析[J].中华皮肤科杂志,2006,39(10):571-573. 被引量:10
  • 3黄正吉 邱丙森.节段性透明性血管炎26例分析[J].中华皮肤科杂志,1998,21(6):369-371.
  • 4Evereklioglu C, Turkoz Y, Er H, et al. Increased nitric oxide production in patients with Behcet's disease: is it a new activity marker? J Am Acad Dermatol, 2002, 46(1) :50 - 54.
  • 5Heeringa P, Bijl M, de Jager-Krikken A, et al. Renal expression of endothelial and inducible nitric oxide synthase, and formation of peroxynitrite-modified proteins and reactive oxygen species in Wegener's granulomatosis. J Pathol, 2001, 193(2) :224 - 232.
  • 6Tasci B, Direskeneli H, Serdaroglu P, et al. Humoral immune response to mycobacterial heat shock protein (hsp)65 in the cerebrospinal fluid of neuro-Behcet patients. Clin Exp Immunol, 1998, 113(1):100-104.
  • 7Rongioletti F, Ghio L, Ginevri F, et al. Purpura of the ears: a distinctive vasculopathy with circulating autoantibodies complicating long-term treatment with levamisole in children. Br J Dermatol, 1999, 140(5) :948 -951.
  • 8Wisnieski JJ. Urticarial vasculitis. Curr Opin Rheumatol, 2000, 12(1) :24 -31.
  • 9Lee LA. Behcet disease. Semin Cutan Med Surg, 2001,20(1) :53 -57.
  • 10Calamia KT, Balabanova M, Perniciaro C, et al. Livedo (livedoid) vasculitis and the factor V Leiden mutation: additional evidence for abnormal coagulation. J Am Acad Dermatol, 2002, 46(1) : 133 -137.

共引文献28

同被引文献47

  • 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
  • 3Rothman S, Block M, Hauser FV. Sjogren's syndrome associated with lymphoblastoma and hypersplenism[J]. AMA Arch Derm Syphilol, 1951,63 : 642-643.
  • 4Bridges A J, England DM. Benign lymphoepithelial lesion: relationship to Sjogren's syndrome and evolving malignant lymphoma[J].Semin Athritis Rheum, 1989,19:201-208.
  • 5Sutcliffe N, Inanc M, Speight P, et al. Predictors of lymphoma development of primary Sjogren's syndrome[J].Semin Arthritis Rheum, 1998,28.. 80-87.
  • 6Kassan SS, Thomas TL, Moutsopoulos HM, et al. Increased risk of lymphoma in sicca syndrome[J].Ann Intern Med, 1978,89: 888- 892.
  • 7Manganelli P, Fietta P, Quaini tv. Hematologic manifestations of primary Sjogren ' s syndrome[J]. Clin Exp Rheumatol, 2006,24:438-448.
  • 8Siegel RS, Pandolfino T, Guitart J, et al. Primary cutaneous T-cell lymphoma: Review and current concepts[J].J Clin Oncol, 2000,18(15):2908.
  • 9Kempf W, Dummer R, Burg G. Approach to lymphoproliferative infilt rates of the skin, the difficult lesions[J]. Am J ClinPathol, 1999,111(Suppl. 1):584-593.
  • 10Theander E, Henriksson G, Ljungberg O, et al. Lymphoma and other malignancies in primary Sjogren's syndrome: a cohort study on cancer incidence and lymphoma predictors[J].Ann Rheum Dis, 2006,65 : 796-803.

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