Acquired hemophagocytic lymphohistiocytosis as initial manifestation of multiple myeloma: A case report and literature review

INTRODUCTION: Hemophagocytic lymphohistiocytosis (HLH) is a condition characterized by a hyperinflammatory state and persistent macrophage activation, resulting in reactive phagocytosis of the hematopoietic elements. In children, it is usually a hereditary disorder, while in adults it is usually acq...

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Dades bibliogràfiques
Publicat a:Medicine (Baltimore)
Autors principals: Mendes, Fernanda Rodrigues, Sobral, Karine Marques, Culler, Hebert Fabricio, Couto, Samuel Campanelli Freitas, Pereira, Juliana, Rocha, Vanderson, Martinez, Gracia Aparecida, Lage, Luís Alberto de Pádua Covas
Format: Artigo
Idioma:Inglês
Publicat: Lippincott Williams & Wilkins 2020
Matèries:
4800
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC7523830/
https://ncbi.nlm.nih.gov/pubmed/32991435
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1097/MD.0000000000022299
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