Severe HELLP syndrome masquerading as thrombocytopenic thrombotic purpura: a case report

BACKGROUND: Thrombotic microangiopathies (TMAs) occurring in the postpartum period may be difficult to manage. They present as the combination of mechanical hemolytic anemia and consumption thrombocytopenia due to endothelial dysfunction. The cause of this endothelial aggression can be multiple: thr...

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Detalles Bibliográficos
Autores principales: Mousseaux, Cyril, Joly, Bérangère S., Mohamadou, Inna, Arrestier, Romain, Hertig, Alexandre, Rafat, Cédric
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7260815/
https://www.ncbi.nlm.nih.gov/pubmed/32471388
http://dx.doi.org/10.1186/s12882-020-01865-y

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7260815/
https://www.ncbi.nlm.nih.gov/pubmed/32471388
http://dx.doi.org/10.1186/s12882-020-01865-y

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