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. 2008 May;3(3):800–807. doi: 10.2215/CJN.04050907

Table 2.

Limitations in the diagnosis of recurrent glomerulonephritidesa

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
a

AG, allograft glomerulopathy.