Hemolytic uremic syndrome caused by Shiga toxin-producing Escherichia coli in a renal transplant recipient case report

Detalhes bibliográficos
Autor(a) principal: Nieto-Rios,John Fredy
Data de Publicação: 2021
Outros Autores: Zuluaga-Quintero,Monica, Valencia-Maturana,Julio Cesar, Bello-Marquez,Diana Carolina, Aristizabal-Alzate,Arbey, Zuluaga-Valencia,Gustavo Adolfo, Serna-Higuita,Lina Maria, Arias,Luis Fernando
Tipo de documento: Relatório
Idioma: eng
Título da fonte: Jornal Brasileiro de Nefrologia
Texto Completo: http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0101-28002021000400591
Resumo: Abstract Thrombotic microangiopathies are disorders characterized by nonimmune microangiopathic hemolytic anemia, thrombocytopenia, and multi-systemic failure. They are classified as thrombotic thrombocytopenic purpura, atypical hemolytic-uremic syndrome, and typical hemolytic uremic syndrome. The latter is associated with intestinal infections by Shiga toxin-producing bacteria. Typical hemolytic uremic syndrome in adults is an extremely rare condition, characterized by high morbidity and mortality. It has been seldom described in solid organ transplant recipients. Here is presented the case of a kidney transplant recipient who had typical hemolytic uremic syndrome with multisystem commitment, refractory to management and with a fatal outcome.
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spelling Hemolytic uremic syndrome caused by Shiga toxin-producing Escherichia coli in a renal transplant recipient case reportThrombotic MicroangiopathiesHemolytic-Uremic SyndromeShiga ToxinKidney TransplantationADAMTS13 ProteinComplement Pathway, Alternative.Abstract Thrombotic microangiopathies are disorders characterized by nonimmune microangiopathic hemolytic anemia, thrombocytopenia, and multi-systemic failure. They are classified as thrombotic thrombocytopenic purpura, atypical hemolytic-uremic syndrome, and typical hemolytic uremic syndrome. The latter is associated with intestinal infections by Shiga toxin-producing bacteria. Typical hemolytic uremic syndrome in adults is an extremely rare condition, characterized by high morbidity and mortality. It has been seldom described in solid organ transplant recipients. Here is presented the case of a kidney transplant recipient who had typical hemolytic uremic syndrome with multisystem commitment, refractory to management and with a fatal outcome.Sociedade Brasileira de Nefrologia2021-12-01info:eu-repo/semantics/reportinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S0101-28002021000400591Brazilian Journal of Nephrology v.43 n.4 2021reponame:Jornal Brasileiro de Nefrologiainstname:Sociedade Brasileira de Nefrologia (SBN)instacron:SBN10.1590/2175-8239-jbn-2020-0048info:eu-repo/semantics/openAccessNieto-Rios,John FredyZuluaga-Quintero,MonicaValencia-Maturana,Julio CesarBello-Marquez,Diana CarolinaAristizabal-Alzate,ArbeyZuluaga-Valencia,Gustavo AdolfoSerna-Higuita,Lina MariaArias,Luis Fernandoeng2021-12-06T00:00:00Zoai:scielo:S0101-28002021000400591Revistahttp://www.bjn.org.br/ONGhttps://old.scielo.br/oai/scielo-oai.php||jbn@sbn.org.br2175-82390101-2800opendoar:2021-12-06T00:00Jornal Brasileiro de Nefrologia - Sociedade Brasileira de Nefrologia (SBN)false
dc.title.none.fl_str_mv Hemolytic uremic syndrome caused by Shiga toxin-producing Escherichia coli in a renal transplant recipient case report
title Hemolytic uremic syndrome caused by Shiga toxin-producing Escherichia coli in a renal transplant recipient case report
spellingShingle Hemolytic uremic syndrome caused by Shiga toxin-producing Escherichia coli in a renal transplant recipient case report
Nieto-Rios,John Fredy
Thrombotic Microangiopathies
Hemolytic-Uremic Syndrome
Shiga Toxin
Kidney Transplantation
ADAMTS13 Protein
Complement Pathway, Alternative.
title_short Hemolytic uremic syndrome caused by Shiga toxin-producing Escherichia coli in a renal transplant recipient case report
title_full Hemolytic uremic syndrome caused by Shiga toxin-producing Escherichia coli in a renal transplant recipient case report
title_fullStr Hemolytic uremic syndrome caused by Shiga toxin-producing Escherichia coli in a renal transplant recipient case report
title_full_unstemmed Hemolytic uremic syndrome caused by Shiga toxin-producing Escherichia coli in a renal transplant recipient case report
title_sort Hemolytic uremic syndrome caused by Shiga toxin-producing Escherichia coli in a renal transplant recipient case report
author Nieto-Rios,John Fredy
author_facet Nieto-Rios,John Fredy
Zuluaga-Quintero,Monica
Valencia-Maturana,Julio Cesar
Bello-Marquez,Diana Carolina
Aristizabal-Alzate,Arbey
Zuluaga-Valencia,Gustavo Adolfo
Serna-Higuita,Lina Maria
Arias,Luis Fernando
author_role author
author2 Zuluaga-Quintero,Monica
Valencia-Maturana,Julio Cesar
Bello-Marquez,Diana Carolina
Aristizabal-Alzate,Arbey
Zuluaga-Valencia,Gustavo Adolfo
Serna-Higuita,Lina Maria
Arias,Luis Fernando
author2_role author
author
author
author
author
author
author
dc.contributor.author.fl_str_mv Nieto-Rios,John Fredy
Zuluaga-Quintero,Monica
Valencia-Maturana,Julio Cesar
Bello-Marquez,Diana Carolina
Aristizabal-Alzate,Arbey
Zuluaga-Valencia,Gustavo Adolfo
Serna-Higuita,Lina Maria
Arias,Luis Fernando
dc.subject.por.fl_str_mv Thrombotic Microangiopathies
Hemolytic-Uremic Syndrome
Shiga Toxin
Kidney Transplantation
ADAMTS13 Protein
Complement Pathway, Alternative.
topic Thrombotic Microangiopathies
Hemolytic-Uremic Syndrome
Shiga Toxin
Kidney Transplantation
ADAMTS13 Protein
Complement Pathway, Alternative.
description Abstract Thrombotic microangiopathies are disorders characterized by nonimmune microangiopathic hemolytic anemia, thrombocytopenia, and multi-systemic failure. They are classified as thrombotic thrombocytopenic purpura, atypical hemolytic-uremic syndrome, and typical hemolytic uremic syndrome. The latter is associated with intestinal infections by Shiga toxin-producing bacteria. Typical hemolytic uremic syndrome in adults is an extremely rare condition, characterized by high morbidity and mortality. It has been seldom described in solid organ transplant recipients. Here is presented the case of a kidney transplant recipient who had typical hemolytic uremic syndrome with multisystem commitment, refractory to management and with a fatal outcome.
publishDate 2021
dc.date.none.fl_str_mv 2021-12-01
dc.type.driver.fl_str_mv info:eu-repo/semantics/report
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
format report
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0101-28002021000400591
url http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0101-28002021000400591
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv 10.1590/2175-8239-jbn-2020-0048
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.43 n.4 2021
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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