Publications by authors named "Julio E Venditti"
Hemophagocytic syndrome (HS) is a severe hyper inflammatory condition whose cardinal symptoms are prolonged fever, cytopenia, hepatosplenomegaly, and hemophagocytosis by activated, morphologically benign macrophages. The clinical course resembles sepsis, sharing similar physiopathological features. We report four patients with the syndrome.
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- A case is presented of a patient with multiple myeloma and giant cell arteritis, highlighting a novel occurrence without the presence of systemic amyloidosis.
- This instance is significant as it marks the first documented case of its kind in medical literature.
- The findings suggest a potential pathogenic relationship between multiple myeloma and giant cell arteritis, warranting further investigation.