Table 2.
Native kidney disease |
unknown in many patients with ESRD |
black patients are often labeled to have hypertensive nephrosclerosis |
difficulties in determining the cause of native kidney disease when presenting at a late stage |
difficulties in differentiating primary versus secondary FSGS |
Indication for posttransplantation renal biopsy |
lack of unified approach in diagnosing patients with posttransplantation proteinuria, hematuria, and renal dysfunction |
non-uniform indications for biopsy: protocol versus clinical renal disease |
immunofluorescence and electron microscopic examinations not routinely performed on all transplant biopsies |
Diagnosis of posttransplantation GN |
lack of histologic features of FSGS in early stage of recurrence |
difficulties in differentiating primary versus secondary FSGS |
difficulties in differentiating MPGN versus AG |
difficulties in differentiating primary versus secondary IgAN |
difficulties in differentiating the cause of HUS/TTP: primary versus drug toxicity versus humoral rejection |
AG, allograft glomerulopathy.