Anemia hemolítica microangiopática en lupus eritematoso sistémico: revision narrativa de la literatura

Nicolas Coronel Restrepo, Carolina Munoz-Grajales, Carlos Jaime Velásquez, Javier Márquez, Luis Fernando Pinto

Producción científica: Contribución a una revistaArtículo de revisiónrevisión exhaustiva


Introduction: The clinical spectrum of microangiopathy disorders is vast, and needs a great clinical skill to find the origin, especially in patients with systemic lupus erythematosus, in whom it is necessary to consider: associated thrombotic thrombocytopenic purpura, antip-hospholipid syndrome, generally of the catastrophic type; localised microangiopathy, or malignant hypertension. Objective: Using the results reported in the literature, the aim of this article is to describe the frequency, causes and clinical features of thrombotic microangiopathy in systemic lupus erythematosus. Methods: Structured non-systematic review of the literature. Results: The review included a total of 51 articles (42 from database searches and 9 referenced in these) on the previously mentioned variables, were included.

Título traducido de la contribuciónIcroangiopathic hemolytic anemia in systemic lupus erythematosus: Narrative review
Idioma originalEspañol
Páginas (desde-hasta)162-167
Número de páginas6
PublicaciónRevista Colombiana de Reumatologia
EstadoPublicada - 2015
Publicado de forma externa

Nota bibliográfica

Publisher Copyright:
© 2015 Asociación Colombiana de Reumatología. Published by Elsevier España, S.L.U. All rights reserved.

Palabras clave

  • Lupus
  • Microangiopathic haemolytic anaemia
  • Systemic lupus erythematosus
  • Thrombotic thrombocytopenic purpura


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