Anca-positive vasculitis with full-house nephropathy, an unusual association: a case report and review of literature
Autor(a) principal: | |
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Data de Publicação: | 2022 |
Outros Autores: | , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Jornal Brasileiro de Nefrologia |
Texto Completo: | http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0101-28002022000200285 |
Resumo: | Abstract Rapidly progressive glomerulonephritis is a medical emergency, with mortality around 20%. It is characterized by crescent glomerulonephritis and progressive loss of kidney function, hematuria, and proteinuria. Its classification is given by immunofluorescence detection of antibodies against glomerular basement membrane (Anti-MBG), immunocomplexes, or pauci-immune pattern. Its etiology should be based on clinical findings, immunological profile, age, sex, and histopathological characteristics. We present a case of a 27-year-old woman with symptoms consistent with rapidly progressive glomerulonephritis and biopsy findings of a full-house kidney nephropathy, with an early fatal outcome. An association of low incidence, as it is a case with a full-house pattern, and an autoimmune profile for negative systemic lupus erythematosus makes this a rare case. ANCA-associated vasculitis with full-house kidney disease was diagnosed, an unusual condition with up to 3% presentation and few reports in the literature, highlighting the importance of its reporting and contribution to the literature. |
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Anca-positive vasculitis with full-house nephropathy, an unusual association: a case report and review of literatureLupus Erythematosus, SystemicAnti-Neutrophil Cytoplasmic Antibody-Associated VasculitisNefropatiasGlomerulonephritisAbstract Rapidly progressive glomerulonephritis is a medical emergency, with mortality around 20%. It is characterized by crescent glomerulonephritis and progressive loss of kidney function, hematuria, and proteinuria. Its classification is given by immunofluorescence detection of antibodies against glomerular basement membrane (Anti-MBG), immunocomplexes, or pauci-immune pattern. Its etiology should be based on clinical findings, immunological profile, age, sex, and histopathological characteristics. We present a case of a 27-year-old woman with symptoms consistent with rapidly progressive glomerulonephritis and biopsy findings of a full-house kidney nephropathy, with an early fatal outcome. An association of low incidence, as it is a case with a full-house pattern, and an autoimmune profile for negative systemic lupus erythematosus makes this a rare case. ANCA-associated vasculitis with full-house kidney disease was diagnosed, an unusual condition with up to 3% presentation and few reports in the literature, highlighting the importance of its reporting and contribution to the literature.Sociedade Brasileira de Nefrologia2022-06-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S0101-28002022000200285Brazilian Journal of Nephrology v.44 n.2 2022reponame:Jornal Brasileiro de Nefrologiainstname:Sociedade Brasileira de Nefrologia (SBN)instacron:SBN10.1590/2175-8239-jbn-2020-0134info:eu-repo/semantics/openAccessMontalvo,Carlos Mauricio MartínezGutierrez,Laura CatalinaPerez,CarolinaDelgado,Harrison HerreraBarrios,Paula Corinna Martinezeng2022-06-21T00:00:00Zoai:scielo:S0101-28002022000200285Revistahttp://www.bjn.org.br/ONGhttps://old.scielo.br/oai/scielo-oai.php||jbn@sbn.org.br2175-82390101-2800opendoar:2022-06-21T00:00Jornal Brasileiro de Nefrologia - Sociedade Brasileira de Nefrologia (SBN)false |
dc.title.none.fl_str_mv |
Anca-positive vasculitis with full-house nephropathy, an unusual association: a case report and review of literature |
title |
Anca-positive vasculitis with full-house nephropathy, an unusual association: a case report and review of literature |
spellingShingle |
Anca-positive vasculitis with full-house nephropathy, an unusual association: a case report and review of literature Montalvo,Carlos Mauricio Martínez Lupus Erythematosus, Systemic Anti-Neutrophil Cytoplasmic Antibody-Associated Vasculitis Nefropatias Glomerulonephritis |
title_short |
Anca-positive vasculitis with full-house nephropathy, an unusual association: a case report and review of literature |
title_full |
Anca-positive vasculitis with full-house nephropathy, an unusual association: a case report and review of literature |
title_fullStr |
Anca-positive vasculitis with full-house nephropathy, an unusual association: a case report and review of literature |
title_full_unstemmed |
Anca-positive vasculitis with full-house nephropathy, an unusual association: a case report and review of literature |
title_sort |
Anca-positive vasculitis with full-house nephropathy, an unusual association: a case report and review of literature |
author |
Montalvo,Carlos Mauricio Martínez |
author_facet |
Montalvo,Carlos Mauricio Martínez Gutierrez,Laura Catalina Perez,Carolina Delgado,Harrison Herrera Barrios,Paula Corinna Martinez |
author_role |
author |
author2 |
Gutierrez,Laura Catalina Perez,Carolina Delgado,Harrison Herrera Barrios,Paula Corinna Martinez |
author2_role |
author author author author |
dc.contributor.author.fl_str_mv |
Montalvo,Carlos Mauricio Martínez Gutierrez,Laura Catalina Perez,Carolina Delgado,Harrison Herrera Barrios,Paula Corinna Martinez |
dc.subject.por.fl_str_mv |
Lupus Erythematosus, Systemic Anti-Neutrophil Cytoplasmic Antibody-Associated Vasculitis Nefropatias Glomerulonephritis |
topic |
Lupus Erythematosus, Systemic Anti-Neutrophil Cytoplasmic Antibody-Associated Vasculitis Nefropatias Glomerulonephritis |
description |
Abstract Rapidly progressive glomerulonephritis is a medical emergency, with mortality around 20%. It is characterized by crescent glomerulonephritis and progressive loss of kidney function, hematuria, and proteinuria. Its classification is given by immunofluorescence detection of antibodies against glomerular basement membrane (Anti-MBG), immunocomplexes, or pauci-immune pattern. Its etiology should be based on clinical findings, immunological profile, age, sex, and histopathological characteristics. We present a case of a 27-year-old woman with symptoms consistent with rapidly progressive glomerulonephritis and biopsy findings of a full-house kidney nephropathy, with an early fatal outcome. An association of low incidence, as it is a case with a full-house pattern, and an autoimmune profile for negative systemic lupus erythematosus makes this a rare case. ANCA-associated vasculitis with full-house kidney disease was diagnosed, an unusual condition with up to 3% presentation and few reports in the literature, highlighting the importance of its reporting and contribution to the literature. |
publishDate |
2022 |
dc.date.none.fl_str_mv |
2022-06-01 |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0101-28002022000200285 |
url |
http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0101-28002022000200285 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
10.1590/2175-8239-jbn-2020-0134 |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
text/html |
dc.publisher.none.fl_str_mv |
Sociedade Brasileira de Nefrologia |
publisher.none.fl_str_mv |
Sociedade Brasileira de Nefrologia |
dc.source.none.fl_str_mv |
Brazilian Journal of Nephrology v.44 n.2 2022 reponame:Jornal Brasileiro de Nefrologia instname:Sociedade Brasileira de Nefrologia (SBN) instacron:SBN |
instname_str |
Sociedade Brasileira de Nefrologia (SBN) |
instacron_str |
SBN |
institution |
SBN |
reponame_str |
Jornal Brasileiro de Nefrologia |
collection |
Jornal Brasileiro de Nefrologia |
repository.name.fl_str_mv |
Jornal Brasileiro de Nefrologia - Sociedade Brasileira de Nefrologia (SBN) |
repository.mail.fl_str_mv |
||jbn@sbn.org.br |
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1752122067387416576 |