| Literature DB >> 25914879 |
Song Yi Han1, Seung Ik Lee1, Yeon Hee Lee1, Ae Jin Kim1, Hye Jin Lim1, Han Ro2, Jae Hyun Chang2, Hyun Hee Lee2, Wookyung Chung2, Ji Yong Jung2.
Abstract
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.Entities:
Keywords: Immunoglobulin G; Kidney; Sclerosis
Year: 2015 PMID: 25914879 PMCID: PMC4406993 DOI: 10.4068/cmj.2015.51.1.39
Source DB: PubMed Journal: Chonnam Med J ISSN: 2233-7393