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Idiopathic nodular glomerulosclerosis: Report of two cases and review of literature

Nodular glomerulosclerosis, a pathological finding characterized by areas of marked mesangial expansion with accentuated glomerular nodularity can be seen in a number of conditions including diabetic nephropathy, amyloidosis, light chain deposition disease, fibrillary and immunotactoid glomerulopath...

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Autores principales: Chandragiri, S., Raju, S., Mukku, K. K., Babu, S., Uppin, M. S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4795433/
https://www.ncbi.nlm.nih.gov/pubmed/27051142
http://dx.doi.org/10.4103/0971-4065.164233
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author Chandragiri, S.
Raju, S.
Mukku, K. K.
Babu, S.
Uppin, M. S.
author_facet Chandragiri, S.
Raju, S.
Mukku, K. K.
Babu, S.
Uppin, M. S.
author_sort Chandragiri, S.
collection PubMed
description Nodular glomerulosclerosis, a pathological finding characterized by areas of marked mesangial expansion with accentuated glomerular nodularity can be seen in a number of conditions including diabetic nephropathy, amyloidosis, light chain deposition disease, fibrillary and immunotactoid glomerulopathy, collagen type III disease, nodular membranoproliferative glomerulonephritis, and Takayasu's arteritis. Idiopathic nodular glomerulosclerosis is a diagnosis of exclusion and is reported in patients with hypertension, smoking, chronic obstructive pulmonary disease, obesity, metabolic syndrome, etc. We report two cases of idiopathic nodular glomerulosclerosis, one in obese hypertensive male and the other in nonhypertensive, nonobese female patient.
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spelling pubmed-47954332016-04-05 Idiopathic nodular glomerulosclerosis: Report of two cases and review of literature Chandragiri, S. Raju, S. Mukku, K. K. Babu, S. Uppin, M. S. Indian J Nephrol Case Report Nodular glomerulosclerosis, a pathological finding characterized by areas of marked mesangial expansion with accentuated glomerular nodularity can be seen in a number of conditions including diabetic nephropathy, amyloidosis, light chain deposition disease, fibrillary and immunotactoid glomerulopathy, collagen type III disease, nodular membranoproliferative glomerulonephritis, and Takayasu's arteritis. Idiopathic nodular glomerulosclerosis is a diagnosis of exclusion and is reported in patients with hypertension, smoking, chronic obstructive pulmonary disease, obesity, metabolic syndrome, etc. We report two cases of idiopathic nodular glomerulosclerosis, one in obese hypertensive male and the other in nonhypertensive, nonobese female patient. Medknow Publications & Media Pvt Ltd 2016 /pmc/articles/PMC4795433/ /pubmed/27051142 http://dx.doi.org/10.4103/0971-4065.164233 Text en Copyright: © 2016 Indian Journal of Nephrology http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 3.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as the author is credited and the new creations are licensed under the identical terms.
spellingShingle Case Report
Chandragiri, S.
Raju, S.
Mukku, K. K.
Babu, S.
Uppin, M. S.
Idiopathic nodular glomerulosclerosis: Report of two cases and review of literature
title Idiopathic nodular glomerulosclerosis: Report of two cases and review of literature
title_full Idiopathic nodular glomerulosclerosis: Report of two cases and review of literature
title_fullStr Idiopathic nodular glomerulosclerosis: Report of two cases and review of literature
title_full_unstemmed Idiopathic nodular glomerulosclerosis: Report of two cases and review of literature
title_short Idiopathic nodular glomerulosclerosis: Report of two cases and review of literature
title_sort idiopathic nodular glomerulosclerosis: report of two cases and review of literature
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4795433/
https://www.ncbi.nlm.nih.gov/pubmed/27051142
http://dx.doi.org/10.4103/0971-4065.164233
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