IgG4-Related Systemic Disease Can Be Easily Mistaken as a Uroepithelial Tumor

نویسندگان

  • Song Yi Han
  • Seung Ik Lee
  • Yeon Hee Lee
  • Ae Jin Kim
  • Hye Jin Lim
  • Han Ro
  • Jae Hyun Chang
  • Hyun Hee Lee
  • Wookyung Chung
  • Ji Yong Jung
چکیده

Immunoglobulin G4-related disease (IgG4-RD) is a newly recognized systemic syndrome characterized by elevated serum IgG4 concentrations and tumefaction or tissue infiltration by IgG4-positive plasma cells. We experienced a case of IgG4-RD involving multiple organs in a 64-year-old female who was referred for a suspected uroepithelial tumor. A mass biopsy confirmed dense lymphoplasmacytic infiltration with an increased number of IgG4-positive plasma cells. We discuss this case and review the literature to bring IgG4-RD to the attention to clinicians because it responds dramatically well to steroid therapy and should be kept in mind as a differential diagnosis to avoid unnecessary surgery.

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عنوان ژورنال:

دوره 51  شماره 

صفحات  -

تاریخ انتشار 2015