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dc.contributor.authorBulger, Madison
dc.date.issued2021
dc.description.abstract"Hemophagocytic lymphohistiocytosis (HLH) is a rare, life-threatening syndrome of excessive immune activation that can be acquired genetically or sporadically. It is triggered by events that disrupt immune function and has a variable presentation that has a median survival of 2 months without prompt treatment. Tularemia is a highly infectious zoonotic illness caused by Francisella tularensis that most commonly results in ulcero-glandular disease. We have been unable to find previously documented cases of HLH secondary to tularemia."--Introduction.eng
dc.identifier.urihttps://hdl.handle.net/10355/90921
dc.rightsOpenAccess.eng
dc.rights.licenseThis work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivs 3.0 License.
dc.titleRare case of hemophagocytic lymphohistiocytosis secondary to tularemiaeng
dc.typeOthereng


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