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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| Main Authors: | , , , , , |
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| Format: | Book |
| Published: |
University of São Paulo,
2021-08-01T00:00:00Z.
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| Online Access: | Connect to this object online. |
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