期刊文献+

复发性皮肤坏死性嗜酸性血管炎

A case of recurrent cutaneous necrotizing eosinophilic vasculitis
下载PDF
导出
摘要 报告1例复发性皮肤坏死性嗜酸性血管炎。患者男,57岁。全身散在结节、斑块、结痂1个月余。皮肤科检查:面部满布厚黑焦痂,四肢散在同样皮疹,呈圆环状。皮损组织病理检查示:表皮坏死,真皮全层脂肪小叶及间隙内可见大量增生扩张的血管,部分血管壁纤维蛋白样变性,红细胞外溢,伴大量嗜酸性粒细胞、淋巴细胞浸润。诊断:复发性皮肤坏死性嗜酸性血管炎。治疗:口服糖皮质激素联合硫唑嘌呤有效。 A 57-years-old man presented with disseminated nodules, plaques, black thick eschar on his whole body 1 month ago. Skin examination revealed black thick eschar on the face, the same circinal rash on the limbs. Histopathology examination showed epidermal necrosis, a large number of proliferation of the vascular in the whole dermis fat leaflet and interval, fibriuoid degeneration on the wall of some vessels, red blood cell overflow with prominent eosinophilic and lymphocytes infiltrating. A diagnosis of recurrent cutaneous necrotizing eosinophilic vasculitis was made. The lesions improved markedly after treatment with oral glucocorticoid and azathioprine.
作者 刘丹 巴伟 杨怡 李承新 LIU Dan BA Wei YANC Yi LI Cheng-xin(Department of Dermatology, Chinese PLA General Hospital, Beijing 100853, China)
出处 《临床皮肤科杂志》 CAS CSCD 北大核心 2016年第10期717-719,共3页 Journal of Clinical Dermatology
关键词 血管炎 嗜酸性 皮肤坏死性 vasculitis, eosinophilic, cutaneous necrotizing
  • 相关文献

参考文献5

二级参考文献12

  • 1周春丽,宋志强,向明明,叶庆佾,郝飞.嗜酸性粒细胞增多综合征1例[J].临床皮肤科杂志,2004,33(12):744-746. 被引量:8
  • 2宋琳毅,曾学思,孙建方.复发性皮肤坏死性嗜酸性血管炎一例[J].中华皮肤科杂志,2005,38(11):709-709. 被引量:3
  • 3周娜娜,车雅敏,刘全忠.复发性皮肤坏死性嗜酸性血管炎[J].中国麻风皮肤病杂志,2007,23(5):429-430. 被引量:2
  • 4Gleich GJ, Leiferman KM, Pardanani A, et al. Treatment of hypereosinophilic syndrome with imatinib mesilate[J]. Lancet, 2002,359(9317): 1577-1578.
  • 5Ueno NT, Anagnostopoulos A, Rondon G, et al. Successful nonmyeloablative allogeneic transplantation for treatment of idiopathic hypereosinophilic syndrome[J]. Br J Haematol, 2002, 119(1):131-134.
  • 6Simon HU, Plotz SG, Dummer R, et al. Abnormal clones of T cells producing interleukin-5 in idiopathic eosinophilia[J]. N Engl J Med, 1999, 341(15): 1112-1120.
  • 7Doorduijn JK, van Lom K, Lowenberg B. Eosinophilia and granulocytic dysplasia terminating in acute myeloid leukaemia after 24 years[J]. Br J Haematol, 1996, 95(3): 531-534.
  • 8Offidani A, Bernardini ML, Simonetti O, et al. Hypereosinophilic dermatosis: skin lesions as the only manifestation of the idiopathic hypereosinophilic syndrome?[J]. Br J Dermatol, 2000, 143(3): 675-677.
  • 9Yoon TY, Ahn GB, Chang SH. Complete remission of hypereosinophilic syndrome after interferon-alpha therapy: report of a case and literature review[J]. J Dermatol, 2000, 27(2): 110-115.
  • 10Offidani A,Bemardini ML,Simonetti O,et al.Hypereosinophilic dermatosis:skin lesions as the only manifestation of the idiopathic hypereosinophilic syndrome?[J].Br J Dermatol,2000,143(3):675-677.

共引文献12

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