Immunotactoid Glomerulopathy of 10-Years’ Duration: Insights Gained From Sequential Biopsies
نویسندگان
چکیده
Camillo Carrara, Elizabeth Ferucci, Stephano Emili, Mirna N. Toukatly, Roberto F. Nicosia and Charles E. Alpers Department of Pathology, University of Washington Medical Center, Seattle, Washington, USA; IRCCS–Mario Negri Institute for Pharmacological Research, Clinical Research Center for Rare Diseases Aldo & Cele Daccò, Bergamo, Italy; Alaska Native Tribal Health Consortium, Anchorage, Alaska, USA; Aurora Kidney LLC, Anchorage, Alaska, USA; and Pathology and Laboratory Medicine Service, VA Puget Sound Health Care System, Seattle, Washington, USA
منابع مشابه
Fibrillary glomerulonephritis and immunotactoid glomerulopathy.
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BACKGROUND Immunotactoid glomerulopathy (ITG) is a rare cause of proteinuria characterized by organized microtubular deposits in the glomerulus. ITG has been associated with underlying lymphoproliferative disorders and any renal impairment may be reversible with treatment of the concomitant hematologic malignancy. This case is the first reported in literature where diffuse large B cell lymphoma...
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عنوان ژورنال:
دوره 2 شماره
صفحات -
تاریخ انتشار 2017