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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...
| Autores principales: | , , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
BioMed Central
2020
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| Materias: | |
| 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 |