TTP-like syndrome associated with hemoglobin SC disease treated successfully with plasma and red cell exchange

BACKGROUND: Sickle cell hemoglobinopathies are associated with end organ damage but very rarely present with a clinical and laboratory picture of microangiopathic hemolytic anemia (MAHA) and thrombocytopenia, characteristic of thrombotic microangiopathy (TMA). CASE PRESENTATION: We present a patient...

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Detalles Bibliográficos
Autores principales: Kodali, Sreenath, Ramachandran, Preethi, Richard, Ivan N., Wang, Jen-Chin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2019
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6676459/
https://www.ncbi.nlm.nih.gov/pubmed/31388486
http://dx.doi.org/10.1016/j.lrr.2019.100179

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6676459/
https://www.ncbi.nlm.nih.gov/pubmed/31388486
http://dx.doi.org/10.1016/j.lrr.2019.100179

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