9 results match your criteria: "USA. anthony.chang@uchospitals.edu[Affiliation]"
Transpl Int
October 2012
Departments of Pathology, University of Chicago Medical Center, Chicago, IL 60637, USA.
The contribution of T cells and graft-reactive antibodies to acute allograft rejection is widely accepted, but the role of graft-infiltrating B and plasma cells is controversial. We examined 56 consecutive human renal transplant biopsies classified by Banff schema into T-cell-mediated (N = 21), antibody-mediated (N = 18), and mixed (N = 17) acute rejection, using standard immunohistochemistry for CD3, CD20, CD138, and CD45. In a predominantly African-American population (75%), neither Banff classification nor C4d deposition predicted the return to dialysis.
View Article and Find Full Text PDFClin J Am Soc Nephrol
August 2012
Department of Pathology, University of Chicago Medical Center, Chicago, Illinois 60607, USA.
The biopsy report for nonneoplastic kidney diseases represents a complex integration of clinical data with light, immunofluorescence, and electron microscopic findings. Practice guidelines for the handling and processing of the renal biopsy have previously been created. However, specific guidelines for essential pathologic parameters that should be included in these pathology reports do not exist.
View Article and Find Full Text PDFHum Pathol
August 2012
Department of Pathology, University of Chicago Medical Center, Chicago, IL 60607, USA.
The biopsy report for nonneoplastic kidney diseases represents a complex integration of clinical data with light, immunofluorescence, and electron microscopic findings. Practice guidelines for the handling and processing of the renal biopsy have previously been created. However, specific guidelines for essential pathologic parameters that should be included in these pathology reports do not exist.
View Article and Find Full Text PDFClin J Am Soc Nephrol
September 2007
University of Chicago Medical Center, Department of Pathology, 5841 S. Maryland Avenue, Room S-628 (MC6101), Chicago, IL 60637, USA.
Background And Objectives: Hematopoietic cell transplantation is a common treatment option for a variety of hematopoietic malignancies. As a result of the use of total body irradiation and/or chemotherapeutic agents, renal dysfunction often ensues. Many pharmacologic agents, such as cyclosporine and high-intensity conditioning regimens, have been linked with thrombotic microangiopathy.
View Article and Find Full Text PDFClin J Am Soc Nephrol
September 2006
Department of Pathology, University of Washington Medical Center, Seattle, Washington, USA.
This paper presents two elderly patients who had normal baseline renal function and had stenotic valvular lesions secondary to rheumatic fever and underwent aortic valve replacements with mechanical valves. Both patients developed acute renal failure after cardiac valve replacement procedures. The renal biopsies revealed acute granulomatous tubulointerstitial nephritis.
View Article and Find Full Text PDFClin Nephrol
December 2006
Department of Pathology, University of Washington Medical Center, Seattle, WA, USA.
Background: IgA nephropathy is the most common glomerulonephritis in the world. Thrombotic microangiopathy occurs in a number of clinical settings, including but not limited to thrombotic thrombocytopenic purpura/hemolytic uremic syndrome, malignant hypertension, anti-phospholipid antibody syndrome and radiation nephropathy. Renovascular complications, such as thrombotic microangiopathy, in the setting of IgA nephropathy may be overlooked and their significance as a concomitant histologic finding is unclear.
View Article and Find Full Text PDFKidney Int
February 2007
Department of Pathology, University of Chicago, Chicago, Illinois 60637, USA.
Am J Kidney Dis
May 2005
Department of Pathology, University of Washington Medical Center, Seattle, WA, USA.
Mod Pathol
July 2005
Department of Pathology, University of Washington Medical Center, Seattle, WA, USA.
We report an unusual histologic manifestation of light chain deposition disease in a 69-year-old female patient, who presented with nephrotic syndrome and an increased serum creatinine. The renal biopsy findings by light and electron microscopy suggested a glomerulonephritis with massive immune-complex deposition, such as lupus nephritis. However, the overall clinical scenario was inconsistent with lupus.
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