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diagnosis hematology activation bleeding differential hemophagocytic lymphohistiocytosis macrophage mas pmr polymyalgia rheumatica summary syndrome treatment
Hemophagocytic Lymphohistiocytosis (HLH) Pathophysiology: Triggering factor (infection,...)→Activation of CD8 T cells (IFN-y) → Excessive activation of macrophages
disrupts immune homeostasis ... Fibrinogen level, ↑ sIL ... Leishmaniosis, malaria ... Lymphohistiocytosis #diagnosis #management ... treatment #summary #rheumatology
Macrophage Activation Syndrome (MAS) Classified among the secondary or acquired forms of haemophagocytic lymphohistiocytosis (sHLH) What? A subset of
lymphohistiocytosis (HLH ... manifestations: from easy bruising ... with leukopenia, anemia ... Syndrome #Diagnosis #Management ... #Hematology #Rheumatology
Bleeding and Bruising - Disorders of Hemostasis - Differential Diagnosis Framework == Quantitative or Qualitative defect in
Bleeding and Bruising ... - Disorders of Hemostasis ... inhibitor and lupus ... of factor VII should ... discern these causes
Polymyalgia Rheumatica (PMR) Diagnosis and Management Summary WHAT? • Polymyalgia rheumatica (PMR) is a common systemic inflammatory
Diagnosis and Management ... disease of unknown cause ... greater than 6 dL ... • Normocytic anemia ... #Rheumatology
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