Idiopathic nodular glomerulosclerosis and differential diagnosis

ABSTRACT Introduction: Idiopathic nodular glomerulosclerosis (ING) is a condition that has a vasculopathic glomerular histological pattern. Case presentation: The authors present the case of a 44-year-old Hispanic smoker female with hypertension and peripheral arterial disease who presented nephroti...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Hauptverfasser: Solares, Sergio Raúl Alvizures, Ibarra-Sifuentes, Héctor Raúl, Ramírez, María Guadalupe Ramírez, Muller, Giovanna Yazmin Arteaga, Valdez, Jesús Cruz
Format: Dataset
Sprache:eng
Schlagworte:
Online-Zugang:Volltext bestellen
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page
container_issue
container_start_page
container_title
container_volume
creator Solares, Sergio Raúl Alvizures
Ibarra-Sifuentes, Héctor Raúl
Ramírez, María Guadalupe Ramírez
Muller, Giovanna Yazmin Arteaga
Valdez, Jesús Cruz
description ABSTRACT Introduction: Idiopathic nodular glomerulosclerosis (ING) is a condition that has a vasculopathic glomerular histological pattern. Case presentation: The authors present the case of a 44-year-old Hispanic smoker female with hypertension and peripheral arterial disease who presented nephrotic syndrome for 2 weeks. The patient was diagnosed with ING by percutaneous renal biopsy results, which showed global nodular mesangial matrix expansion, with linear staining accentuation of glomerular and tubular basement membrane for Immunoglobulin G (IgG) and albumin on immunofluorescence. Conclusions: ING is a rare disease with a poor renal prognosis and wide diagnostic approach; we highlight the importance of analyzing every piece of detail together to reach a definitive diagnosis.
doi_str_mv 10.6084/m9.figshare.14319399
format Dataset
fullrecord <record><control><sourceid>datacite_PQ8</sourceid><recordid>TN_cdi_datacite_primary_10_6084_m9_figshare_14319399</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>10_6084_m9_figshare_14319399</sourcerecordid><originalsourceid>FETCH-LOGICAL-d919-d37d2d9bc869aef5375944e389a860232684f10f3e5578a131281f80b1d599ad3</originalsourceid><addsrcrecordid>eNo1z81qwzAQBGBdeihp36AHv4BdySvZ2ltL6E8g0EvuYuOVHIFsBdk59O3b0OY0DAMDnxBPSjadtPp5wibEcTlR8Y3SoBAQ78XLjmM-03qKQzVnviQq1Zjy5Msl5WVIvuQlLhXNXHEMwRc_r5HSb6Fxvk4P4i5QWvzjf27E4f3tsP2s918fu-3rvmZUWDP03DIeB9sh-WCgN6i1B4tkO9lC21kdlAzgjektKVCtVcHKo2KDSAwbof9umVYa4urducSJyrdT0l19bkJ387mbD34AAi5MxQ</addsrcrecordid><sourcetype>Publisher</sourcetype><iscdi>true</iscdi><recordtype>dataset</recordtype></control><display><type>dataset</type><title>Idiopathic nodular glomerulosclerosis and differential diagnosis</title><source>DataCite</source><creator>Solares, Sergio Raúl Alvizures ; Ibarra-Sifuentes, Héctor Raúl ; Ramírez, María Guadalupe Ramírez ; Muller, Giovanna Yazmin Arteaga ; Valdez, Jesús Cruz</creator><creatorcontrib>Solares, Sergio Raúl Alvizures ; Ibarra-Sifuentes, Héctor Raúl ; Ramírez, María Guadalupe Ramírez ; Muller, Giovanna Yazmin Arteaga ; Valdez, Jesús Cruz</creatorcontrib><description>ABSTRACT Introduction: Idiopathic nodular glomerulosclerosis (ING) is a condition that has a vasculopathic glomerular histological pattern. Case presentation: The authors present the case of a 44-year-old Hispanic smoker female with hypertension and peripheral arterial disease who presented nephrotic syndrome for 2 weeks. The patient was diagnosed with ING by percutaneous renal biopsy results, which showed global nodular mesangial matrix expansion, with linear staining accentuation of glomerular and tubular basement membrane for Immunoglobulin G (IgG) and albumin on immunofluorescence. Conclusions: ING is a rare disease with a poor renal prognosis and wide diagnostic approach; we highlight the importance of analyzing every piece of detail together to reach a definitive diagnosis.</description><identifier>DOI: 10.6084/m9.figshare.14319399</identifier><language>eng</language><publisher>SciELO journals</publisher><subject>FOS: Clinical medicine ; Nephrology and Urology</subject><creationdate>2021</creationdate><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>778,1890</link.rule.ids><linktorsrc>$$Uhttps://commons.datacite.org/doi.org/10.6084/m9.figshare.14319399$$EView_record_in_DataCite.org$$FView_record_in_$$GDataCite.org$$Hfree_for_read</linktorsrc></links><search><creatorcontrib>Solares, Sergio Raúl Alvizures</creatorcontrib><creatorcontrib>Ibarra-Sifuentes, Héctor Raúl</creatorcontrib><creatorcontrib>Ramírez, María Guadalupe Ramírez</creatorcontrib><creatorcontrib>Muller, Giovanna Yazmin Arteaga</creatorcontrib><creatorcontrib>Valdez, Jesús Cruz</creatorcontrib><title>Idiopathic nodular glomerulosclerosis and differential diagnosis</title><description>ABSTRACT Introduction: Idiopathic nodular glomerulosclerosis (ING) is a condition that has a vasculopathic glomerular histological pattern. Case presentation: The authors present the case of a 44-year-old Hispanic smoker female with hypertension and peripheral arterial disease who presented nephrotic syndrome for 2 weeks. The patient was diagnosed with ING by percutaneous renal biopsy results, which showed global nodular mesangial matrix expansion, with linear staining accentuation of glomerular and tubular basement membrane for Immunoglobulin G (IgG) and albumin on immunofluorescence. Conclusions: ING is a rare disease with a poor renal prognosis and wide diagnostic approach; we highlight the importance of analyzing every piece of detail together to reach a definitive diagnosis.</description><subject>FOS: Clinical medicine</subject><subject>Nephrology and Urology</subject><fulltext>true</fulltext><rsrctype>dataset</rsrctype><creationdate>2021</creationdate><recordtype>dataset</recordtype><sourceid>PQ8</sourceid><recordid>eNo1z81qwzAQBGBdeihp36AHv4BdySvZ2ltL6E8g0EvuYuOVHIFsBdk59O3b0OY0DAMDnxBPSjadtPp5wibEcTlR8Y3SoBAQ78XLjmM-03qKQzVnviQq1Zjy5Msl5WVIvuQlLhXNXHEMwRc_r5HSb6Fxvk4P4i5QWvzjf27E4f3tsP2s918fu-3rvmZUWDP03DIeB9sh-WCgN6i1B4tkO9lC21kdlAzgjektKVCtVcHKo2KDSAwbof9umVYa4urducSJyrdT0l19bkJ387mbD34AAi5MxQ</recordid><startdate>20210326</startdate><enddate>20210326</enddate><creator>Solares, Sergio Raúl Alvizures</creator><creator>Ibarra-Sifuentes, Héctor Raúl</creator><creator>Ramírez, María Guadalupe Ramírez</creator><creator>Muller, Giovanna Yazmin Arteaga</creator><creator>Valdez, Jesús Cruz</creator><general>SciELO journals</general><scope>DYCCY</scope><scope>PQ8</scope></search><sort><creationdate>20210326</creationdate><title>Idiopathic nodular glomerulosclerosis and differential diagnosis</title><author>Solares, Sergio Raúl Alvizures ; Ibarra-Sifuentes, Héctor Raúl ; Ramírez, María Guadalupe Ramírez ; Muller, Giovanna Yazmin Arteaga ; Valdez, Jesús Cruz</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-d919-d37d2d9bc869aef5375944e389a860232684f10f3e5578a131281f80b1d599ad3</frbrgroupid><rsrctype>datasets</rsrctype><prefilter>datasets</prefilter><language>eng</language><creationdate>2021</creationdate><topic>FOS: Clinical medicine</topic><topic>Nephrology and Urology</topic><toplevel>online_resources</toplevel><creatorcontrib>Solares, Sergio Raúl Alvizures</creatorcontrib><creatorcontrib>Ibarra-Sifuentes, Héctor Raúl</creatorcontrib><creatorcontrib>Ramírez, María Guadalupe Ramírez</creatorcontrib><creatorcontrib>Muller, Giovanna Yazmin Arteaga</creatorcontrib><creatorcontrib>Valdez, Jesús Cruz</creatorcontrib><collection>DataCite (Open Access)</collection><collection>DataCite</collection></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext_linktorsrc</fulltext></delivery><addata><au>Solares, Sergio Raúl Alvizures</au><au>Ibarra-Sifuentes, Héctor Raúl</au><au>Ramírez, María Guadalupe Ramírez</au><au>Muller, Giovanna Yazmin Arteaga</au><au>Valdez, Jesús Cruz</au><format>book</format><genre>unknown</genre><ristype>DATA</ristype><title>Idiopathic nodular glomerulosclerosis and differential diagnosis</title><date>2021-03-26</date><risdate>2021</risdate><abstract>ABSTRACT Introduction: Idiopathic nodular glomerulosclerosis (ING) is a condition that has a vasculopathic glomerular histological pattern. Case presentation: The authors present the case of a 44-year-old Hispanic smoker female with hypertension and peripheral arterial disease who presented nephrotic syndrome for 2 weeks. The patient was diagnosed with ING by percutaneous renal biopsy results, which showed global nodular mesangial matrix expansion, with linear staining accentuation of glomerular and tubular basement membrane for Immunoglobulin G (IgG) and albumin on immunofluorescence. Conclusions: ING is a rare disease with a poor renal prognosis and wide diagnostic approach; we highlight the importance of analyzing every piece of detail together to reach a definitive diagnosis.</abstract><pub>SciELO journals</pub><doi>10.6084/m9.figshare.14319399</doi><oa>free_for_read</oa></addata></record>
fulltext fulltext_linktorsrc
identifier DOI: 10.6084/m9.figshare.14319399
ispartof
issn
language eng
recordid cdi_datacite_primary_10_6084_m9_figshare_14319399
source DataCite
subjects FOS: Clinical medicine
Nephrology and Urology
title Idiopathic nodular glomerulosclerosis and differential diagnosis
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-16T05%3A37%3A36IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-datacite_PQ8&rft_val_fmt=info:ofi/fmt:kev:mtx:book&rft.genre=unknown&rft.au=Solares,%20Sergio%20Ra%C3%BAl%20Alvizures&rft.date=2021-03-26&rft_id=info:doi/10.6084/m9.figshare.14319399&rft_dat=%3Cdatacite_PQ8%3E10_6084_m9_figshare_14319399%3C/datacite_PQ8%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_id=info:pmid/&rfr_iscdi=true