Evans syndrome in a young man with rare autoimmune associations and transplanted liver

Evans syndrome is classically characterised by two or more cytopenias occurring either concomitantly or sequentially. Most commonly, these are autoimmune haemolytic anaemia and immune thrombocytopenia purpura. It is mostly associated with specific autoimmune conditions such as systemic lupus erythem...

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Detalles Bibliográficos
Autores principales: McCarthy, Matthew Dominic, Fareeth, A G Mohamed
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2022
Materias:
Case Reports: Rare disease
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9528579/
https://www.ncbi.nlm.nih.gov/pubmed/36171014
http://dx.doi.org/10.1136/bcr-2022-251252

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9528579/
https://www.ncbi.nlm.nih.gov/pubmed/36171014
http://dx.doi.org/10.1136/bcr-2022-251252

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