Intermittent Purpura Development Associated with Leukocytoclastic Vasculitis Induced by Infliximab for Crohn's Disease

  • Kishimoto Kenichi
    Department of Internal Medicine II, Shimane University Faculty of Medicine, Japan
  • Kawashima Kousaku
    Department of Internal Medicine II, Shimane University Faculty of Medicine, Japan
  • Fukunaga Mai
    Department of Internal Medicine II, Shimane University Faculty of Medicine, Japan
  • Kotani Satoshi
    Department of Internal Medicine II, Shimane University Faculty of Medicine, Japan
  • Sonoyama Hiroki
    Department of Internal Medicine II, Shimane University Faculty of Medicine, Japan
  • Oka Akihiko
    Department of Internal Medicine II, Shimane University Faculty of Medicine, Japan
  • Mishima Yoshiyuki
    Department of Internal Medicine II, Shimane University Faculty of Medicine, Japan
  • Oshima Naoki
    Department of Internal Medicine II, Shimane University Faculty of Medicine, Japan
  • Ishimura Norihisa
    Department of Internal Medicine II, Shimane University Faculty of Medicine, Japan
  • Ishikawa Noriyoshi
    Department of Pathology, Shimane University Faculty of Medicine, Japan
  • Maruyama Riruke
    Department of Pathology, Shimane University Faculty of Medicine, Japan
  • Ishihara Shunji
    Department of Internal Medicine II, Shimane University Faculty of Medicine, Japan

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抄録

<p>Anti-tumor necrosis factor (TNF) α agents, widely used for the treatment of Crohn's disease (CD), can sometimes induce skin-associated adverse events, which mainly include psoriasis-like eruptions, eczema, and cutaneous infections. In contrast, purpura caused by vasculitis is rarely seen. We herein report a unique case of leukocytoclastic vasculitis induced by infliximab administered for CD in which intermittent purpura development was noted. Fluorescent immunostaining showed no immunoglobulin A deposition on the vessel walls. No purpura was initially seen after starting infliximab, but it appeared approximately 10 months later; however, administration did not have to be discontinued, and the condition was later resolved. The present findings provide important details regarding vasculitis induced by anti-tumor necrosis factor-α agent administration. </p>

収録刊行物

  • Internal Medicine

    Internal Medicine 60 (3), 385-389, 2021-02-01

    一般社団法人 日本内科学会

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