Título : |
Hemolytic uremic syndrome caused by Shiga toxin-producing Escherichia coli in a renal transplant recipient case report |
Tipo de documento : |
documento electrónico |
Autores : |
John Fredy Nieto Ríos, ; Mónica Zuluaga Quintero, ; Arbey Aristizabal Álzate, ; Gustavo Adolfo Zuluaga Valencia, |
Fecha de publicación : |
2021 |
Títulos uniformes : |
Brazilian Journal of Nephrology
|
Idioma : |
Inglés (eng) |
Palabras clave : |
Thrombotic Microangiopathies Hemolytic-Uremic Syndrome Shiga Toxin Kidney Transplantation ADAMTS13 Protein Alternative Complement Pathway |
Resumen : |
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. |
Mención de responsabilidad : |
John Fredy Nieto-Rios, Monica Zuluaga-Quintero, Julio Cesar Valencia-Maturana, Diana Carolina Bello-Marquez, Arbey Aristizabal-Alzate, Gustavo Adolfo Zuluaga-Valencia, Lina Maria Serna-Higuita, Luis Fernando Arias |
Referencia : |
J Bras Nefrol. Oct-Dec 2021;43(4):591-596. |
DOI (Digital Object Identifier) : |
10.1590/2175-8239-jbn-2020-0048 |
PMID : |
33179720 |
Derechos de uso : |
CC BY |
En línea : |
https://bjnephrology.org/en/article/hemolytic-uremic-syndrome-caused-by-shiga-to [...] |
Enlace permanente : |
https://hospitalpablotobon.cloudbiteca.com/pmb/opac_css/index.php?lvl=notice_display&id=5737 |
Hemolytic uremic syndrome caused by Shiga toxin-producing Escherichia coli in a renal transplant recipient case report [documento electrónico] / John Fredy Nieto Ríos, ; Mónica Zuluaga Quintero, ; Arbey Aristizabal Álzate, ; Gustavo Adolfo Zuluaga Valencia, . - 2021. Obra : Brazilian Journal of NephrologyIdioma : Inglés ( eng) Palabras clave : |
Thrombotic Microangiopathies Hemolytic-Uremic Syndrome Shiga Toxin Kidney Transplantation ADAMTS13 Protein Alternative Complement Pathway |
Resumen : |
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. |
Mención de responsabilidad : |
John Fredy Nieto-Rios, Monica Zuluaga-Quintero, Julio Cesar Valencia-Maturana, Diana Carolina Bello-Marquez, Arbey Aristizabal-Alzate, Gustavo Adolfo Zuluaga-Valencia, Lina Maria Serna-Higuita, Luis Fernando Arias |
Referencia : |
J Bras Nefrol. Oct-Dec 2021;43(4):591-596. |
DOI (Digital Object Identifier) : |
10.1590/2175-8239-jbn-2020-0048 |
PMID : |
33179720 |
Derechos de uso : |
CC BY |
En línea : |
https://bjnephrology.org/en/article/hemolytic-uremic-syndrome-caused-by-shiga-to [...] |
Enlace permanente : |
https://hospitalpablotobon.cloudbiteca.com/pmb/opac_css/index.php?lvl=notice_display&id=5737 |
| |