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The glomerular lesions that frequently accompany systemic lupus erythematosus (SLE) have been the subject of intense investigation by clinicians and pathologists for nearly a half-century (1). These efforts have generated numerous attempts to classify and categorize the pathological features of the glomerulonephritis of SLE (lupus nephritis, LN). The work ofdoi:10.1097/01.asn.0000111982.49602.fe pmid:14747399 fatcat:xyhak5iun5fevlzzorot55fn2a