@article{3110295,
    title = "Acute interstitial nephritis and membranous nephropathy in the context of IgG4-related disease",
    author = "Stylianou, K. and Maragkaki, E. and Tzanakakis, M. and Stratakis, S. and Gakiopoulou, H. and Daphnisa, E.",
    journal = "Case Reports in Nephrology and Dialysis",
    year = "2015",
    volume = "5",
    number = "1",
    pages = "44-48",
    publisher = "S Karger AG",
    issn = "2296-9705",
    doi = "10.1159/000369924",
    keywords = "CD20 antigen;  CD3 antigen;  complement component C3;  complement component C4;  complement component C4d;  creatinine;  double stranded DNA antibody;  immunoglobulin G4;  methylprednisolone, adult;  Article;  case report;  cholecystitis;  corticosteroid therapy;  creatinine blood level;  facial nerve paralysis;  human;  human tissue;  immunofluorescence;  immunoglobulin G4 related disease;  immunohistochemistry;  interstitial nephritis;  kidney dysfunction;  kidney tubule basement membrane;  lymphadenopathy;  male;  membranous glomerulonephritis;  middle aged;  priority journal;  sialoadenitis;  vitiligo",
    abstract = "We present the case of a patient with IgG4-related disease, which manifested in an asynchronous manner as vitiligo, cholecystitis, sialadenitis, lymphadenopathy, facial palsy and kidney dysfunction. The patient underwent a renal biopsy, and a presumptive diagnosis of lupus nephritis was made due to compatible clinical and immunological findings. The biopsy revealed IgG4-related kidney disease with severe interstitial nephritis and membranous nephropathy. Corticosteroids treatment restored all disease manifestations. We bring this case to the attention of the nephrologists because of the protean, asynchronous, multisys-temic nature of the disease that necessitates a multidisciplinary approach, a low threshold for kidney biopsy and a high index of suspicion for making the correct diagnosis and treatment. © 2014 S. Karger AG, Basel."
}