Hemophagocytic lymphohistiocytosis presenting as acute coronary syndrome

Acquired Hemophagocytic Lymphohistiocytosis is a rare and deadly syndrome resulting from an overactive immune system, with uncontrolled activation of macrophages and lymphocytes, hypercytokinemia, and systemic inflammatory response. A 75-year-old male presented with typical anginal pain and was diag...

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Vydáno v:Autops Case Rep
Hlavní autoři: Melki, Gabriel, Alkomos, Mina Fransawy, Nanavati, Sushant, Kumar, Vinod, Mariyam, Christina, Maroules, Michael
Médium: Artigo
Jazyk:Inglês
Vydáno: Hospital Universitário da Universidade de São Paulo 2021
Témata:
Clinical Case Report
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC8214879/
https://ncbi.nlm.nih.gov/pubmed/34307236
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4322/acr.2021.285
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