202 results
Polycythemia (Erythrocytosis) - Pathophysiology

#Polycythemia #Erythrocytosis #Pathophysiology #hematology #algorithm #differential #diagnosis
Erythrocytosis) - Pathophysiology ... Erythrocytosis #Pathophysiology ... #hematology #algorithm
Pathophysiology, Signs and Symptoms of Hemolytic Anemia

#Pathophysiology #Hemolytic #Anemia #hematology #diagnosis #signs #symptoms
Pathophysiology, ... Hemolytic Anemia #Pathophysiology ... Hemolytic #Anemia #hematology
Sickle Cell Vaso-Occlusive Crisis

#SickleCell #Crisis #Vasoocclusive #AcuteChestSyndrome #ACS #Pathophysiology #Hematology
AcuteChestSyndrome #ACS #Pathophysiology ... #Hematology
Complement Pathways
- Classical Pathway
- Lectin Pathway
- Alternative Pathway

#Complement #Pathway #hematology #pathophysiology
Complement #Pathway #hematology ... #pathophysiology
Hemolytic anemia in Wilson's disease

#Wilsons #Disease #hemolytic #anemia #Hematology #pathophysiology
hemolytic #anemia #Hematology ... #pathophysiology
Formation of a Hemostatic Platelet Plug

#Hemostatic #Platelet #Plug #Formation #Pathophysiology #Hematology
Plug #Formation #Pathophysiology ... #Hematology
Thromboelastography (TEG) Based Management
 - If R time prolonged -> FFP 
 - If MA low
FFP - If MA low ... TEG #Management #treatment ... #diagnosis #hematology
Thromboelastography (TEG) based therapy and Management

If r time prolonged -> FFP
If MA low -> plts/cryoprecipitate (if
-> FFP If MA low ... Management #Diagnosis #Hematology ... Thromboelastogram #Treatment
Hypereosinophilia and Hypereosinophilic Syndrome

 • Secondary Hypereosinophilic Syndrome
 • Clinically Relevant HES Variants
 • When to
suspect underlying hematologic ... Diagnosis and Treatment ... Syndrome #HES #Hematology
Von Willebrand Disease - Most common inherited bleeding disorder 
Clinical 
 • Easy bruising 
 •
prolonged if very low ... factor VIII) Treatment ... Disease #Diagnosis #Hematology