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Hemophagocytic Lymphohistiocytosis Complicating Systemic Sarcoidosis

Hemophagocytic lymphohistiocytosis (HLH) is a rare, life-threatening hyperinflammatory syndrome characterized by histiocyte proliferation and hemophagocytosis. Primary HLH is caused by genetic defects, whereas secondary HLH occurs in the setting of underlying diseases, such as infections, malignanci...

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Detalles Bibliográficos
Autores principales:	Abughanimeh, Omar, Qasrawi, Ayman, Abu Ghanimeh, Mouhanna
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Cureus 2018
Materias:	Internal Medicine
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6101461/ https://www.ncbi.nlm.nih.gov/pubmed/30131931 http://dx.doi.org/10.7759/cureus.2838

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