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10.1159/000510871 http://scihub22266oqcxt.onion/10.1159/000510871 33363217!7747065!33363217     free     free     free       Case+Rep+Nephrol+Dial 2020 ; 10 (3): 154-162 Nephropedia Template TP {{tp|p=33363217|t=2020. Fibrilo-Tactoid Glomerulonephritis: A Possible Novel Morphological Variant |pdf=|usr=}}{{33363217}} gab.com Text Fibrilo-Tactoid Glomerulonephritis: A Possible Novel Morphological Variant JO: Case Rep Nephrol Dial http://www.kidney.de/pget.php?&tw=1&pmid=33363217 #FOAvip Fibrillary and immunotactoid glomerulonephritis are infrequent causes of primary nephrotic range proteinuria and are poorly understood. Recent significant developments include the discovery of DNA JB9 antigen in fibrillary glomerulonephritis. Here, we present a case of a middle-aged woman who presented with nephrotic range proteinuria, hematuria, and normal renal function. Renal biopsy revealed fibrils that were randomly arranged on electron microscopy. They were of small size and congo red negative similar to the ones found in fibrillary glomerulonephritis, but were also DNA JB 9 negative, and had a hollow core like in immunotactoid glomerulopathy. Though we try to classify these conditions into either immunotactoid glomerulonephropathy (ITGN) or fibrillary glomerulonephritis (FGN), there are scenarios such as this case where it does not fit into either and is probably an overlap or intermediate variant of these two conditions. Pathological features of these glomerulonephrites are discussed together with their clinical implications, treatment choices, and diagnostic importance. Twit Text FOAVip Fibrilo-Tactoid Glomerulonephritis: A Possible Novel Morphological Variant ????Case Rep Nephrol Dial http://www.kidney.de/pget.php?&tw=1&pmid=33363217 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=33363217 #FOAvip English Wikipedia <ref>{{Cite pmid|33363217}}</ref> Fibrilo-Tactoid Glomerulonephritis: A Possible Novel Morphological Variant #MMPMID33363217 Vanga A; Magoon S; Kowalewska J; Mussarat S Case Rep Nephrol Dial 2020[Sep]; 10 (3): 154-162 PMID33363217show ga Fibrillary and immunotactoid glomerulonephritis are infrequent causes of primary nephrotic range proteinuria and are poorly understood. Recent significant developments include the discovery of DNA JB9 antigen in fibrillary glomerulonephritis. Here, we present a case of a middle-aged woman who presented with nephrotic range proteinuria, hematuria, and normal renal function. Renal biopsy revealed fibrils that were randomly arranged on electron microscopy. They were of small size and congo red negative similar to the ones found in fibrillary glomerulonephritis, but were also DNA JB 9 negative, and had a hollow core like in immunotactoid glomerulopathy. Though we try to classify these conditions into either immunotactoid glomerulonephropathy (ITGN) or fibrillary glomerulonephritis (FGN), there are scenarios such as this case where it does not fit into either and is probably an overlap or intermediate variant of these two conditions. Pathological features of these glomerulonephrites are discussed together with their clinical implications, treatment choices, and diagnostic importance. ?Fibrilo-Tactoid Glomerulonephritis: A Possible Novel Morphological Var(epmc).pdf DeepDyve Pubget Overpricing