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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...
Autores principales: | Memon, Fatima, Ahmed, Jawad, Malik, Farheen, Ahmad, Junaid, Memon, Danish Ahmed |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cureus
2020
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Materias: | |
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 |
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