20 results
diagnosis hematology treatment oncology pathophysiology rheumatology syndromes thrombosis acquired activation allergy anticoagulation antiphospholipid apml aps arterial bacteremia causes cd4 classification
Bacteremia Quick Reference - Treatment Duration Gram Negative Bacteremia: • Avoid: Aminoglycosides and tigecycline • Catheters should
Reference - Treatment Duration ... to cefepime • Duration ... the following criteria ... blood cultures drawn ... Bacteremia #Treatment #Management
Acquired von Willebrand Syndrome - Diagnosis and Management • Autoantibodies to vWF: Lymphoproliferative disorders (e.g. lymphoma,
von Willebrand Syndrome ... Diagnosis and Management ... vonWillebrand #Syndrome ... #treatment #hematology ... #differential
Drug Reaction with Eosinophilia and Systemic Symptoms (DRESS) Definition: • Severe adverse drug reaction, characterized by
Criteria for Diagnosis ... Resolution > 15 days Differentials ... SinaiBmoreIMRes #DRESS #Syndrome ... #dermatology #diagnosis ... #management
Venous Thrombosis vs Arterial Thrombosis - Differential Diagnosis Framework VENOUS THROMBOSIS • Acquired Risk Factors: - >48 hours
Arterial Thrombosis - Differential ... Factor V Leiden mutation ... • Nephrotic Syndrome ... pathophysiology #hematology ... #differential #
Hepatopulmonary Syndrome - Diagnosis and Management Summary A defect in arterial oxygenation due to a gas exchange
Hepatopulmonary Syndrome ... Diagnosis and Management ... HPS Diagnostic Criteria ... hepatopulmonary #syndrome ... #diagnosis #management
Polycythemia Vera (PV) - Diagnosis and Management Summary Diagnostic Criteria: • Elevated hemoglobin and/or hematocrit AND •
Diagnosis and Management ... Summary Diagnostic Criteria ... growth AND • JAK2 mutation ... PV #Diagnosis #Management ... Summary #treatment #hematology
Macrophage Activation Syndrome (MAS) Classified among the secondary or acquired forms of haemophagocytic lymphohistiocytosis (sHLH) What? A subset of
Macrophage Activation Syndrome ... Periodic fever syndromes ... Histopathologic criteria ... #Diagnosis #Management ... #Hematology #Rheumatology
Inherited Qualitative Platelet Defects Bernard-Soulier Syndrome • Defect of adhesion due to a lack of GP Ib/IX/V
Bernard-Soulier Syndrome ... mobility due to mutation ... Grey Platelet Syndrome ... comparison #table #differential ... #diagnosis #hematology
2019 EULAR recommendations for thrombosis in (Antiphospholipid Syndrome) APS Venous Thrombosis - Arterial Thrombosis INR Target Duration Recurrence Dr. Laurent ARNAUD
Antiphospholipid Syndrome ... Thrombosis INR Target Duration ... Antiphospholipid #Syndrome ... #APS #management ... #rheumatology #hematology
Hamartomatous Polyposis Syndromes - Peutz-Jeghers Syndrome (PJS), Juvenile Polyposis Syndrome (JPS), Cowden Syndrome (CS), Cronkhite-Canada (CC),
Dominant I STKII Gene Mutation ... Autosomal Dominant I Mutation ... TGF-ß family - Criteria ... " - PTEN gene mutation ... #diagnosis #management
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