Adult-onset Primary Hemophagocytic Lymphohistiocytosis: Reporting a Rare Case with Review of Literature

Hemophagocytic lymphohistiocytosis (HLH) is an uncommon, aggressive hematological syndrome. It is caused by an increased and unchecked proliferation of T lymphocytes and histiocytes. These cells secrete a large number of inflammatory cytokines and infiltrate various tissues causing multi-organ syste...

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Detalles Bibliográficos
Autores principales: Memon, Fatima, Ahmed, Jawad, Malik, Farheen, Ahmad, Junaid, Memon, Danish Ahmed
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cureus 2020
Materias:
Internal Medicine
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7034735/
https://www.ncbi.nlm.nih.gov/pubmed/32133251
http://dx.doi.org/10.7759/cureus.6723

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7034735/
https://www.ncbi.nlm.nih.gov/pubmed/32133251
http://dx.doi.org/10.7759/cureus.6723

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