Cuando Lo Infrecuente Es Lo Mas Probable. Sindrome Hemolitico Ur#xE9;mico Atipico En El Postparto, Reporte De Dos Casos

Authors

  • Carlos Pizarro

  • Carlos Pizarro

  • Carlos Pizarro

  • Silvana Jim#xE9;nez

  • Daniela Osorio

Keywords:

renal insufficiency, postpartum period, atypical hemolytic uremic syndrome, thrombocytopenia

Abstract

Introduction: Hemolytic uremic syndrome in postpartum is an orphan disease, characterized by microangiopathic hemolytic anemia, thrombocytopenia, and acute kidney injury. It occurs due to abnormal complement activation, which activates the membrane attack complex. Pregnancy is characterized by being a pro inflammatory state, which has been related as one of the possible triggers for this pathology. According to its pathophysiology, the use of "Eculizumab" has been established as a gold standard treatment in this pathology. This is a humanized IgG2 monoclonal antibody that blocks the conversion of C5 to C5a, with subsequent inhibition in the formation of the membrane attack complex.

How to Cite

Carlos Pizarro, Carlos Pizarro, Carlos Pizarro, Silvana Jim#xE9;nez, & Daniela Osorio. (2020). Cuando Lo Infrecuente Es Lo Mas Probable. Sindrome Hemolitico Ur#xE9;mico Atipico En El Postparto, Reporte De Dos Casos. Global Journal of Medical Research, 20(E4), 33–39. Retrieved from https://medicalresearchjournal.org/index.php/GJMR/article/view/2136

Cuando Lo Infrecuente Es Lo Mas Probable. Sindrome Hemolitico Ur#xE9;mico Atipico En El Postparto, Reporte De Dos Casos

Published

2020-03-15