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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...
Αποθηκεύτηκε σε:
| Τόπος έκδοσης: | Autops Case Rep |
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| Κύριοι συγγραφείς: | , , , , , |
| Μορφή: | Artigo |
| Γλώσσα: | Inglês |
| Έκδοση: |
Hospital Universitário da Universidade de São Paulo
2021
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| Θέματα: | |
| Διαθέσιμο Online: | 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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