Acute Interstitial Nephritis and Membranous Nephropathy in the Context of IgG4-Related Disease.

Autor: Stylianou K; Nephrology Department, University Hospital of Heraklion, Heraklion, Greece., Maragkaki E; Nephrology Department, University Hospital of Heraklion, Heraklion, Greece., Tzanakakis M; Nephrology Department, University Hospital of Heraklion, Heraklion, Greece., Stratakis S; Nephrology Department, University Hospital of Heraklion, Heraklion, Greece., Gakiopoulou H; Pathology Department, National and Kapodistrian University of Athens, Athens, Greece., Daphnis E; Nephrology Department, University Hospital of Heraklion, Heraklion, Greece.
Jazyk: angličtina
Zdroj: Case reports in nephrology and dialysis [Case Rep Nephrol Dial] 2014 Dec 03; Vol. 5 (1), pp. 44-8. Date of Electronic Publication: 2014 Dec 03 (Print Publication: 2015).
DOI: 10.1159/000369924
Abstrakt: 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, multisystemic 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.
Databáze: MEDLINE
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