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differential management algorithm causes abnormal bleeding disorders lupus prolonged sle syndrome testing thrombocytopenia activation arthritis bruising central chronic cll coagulation
How to Evaluate an Abnormal APTT Step 1: Is the PT or APTT Artifactually Prolonged? Step 2: Is
: Is the PT or APTT ... ) Step 3: Is a Systemic ... Disease Prolonging ... #prolonged #diagnosis ... #hematology #evaluation
Algorithm for the Evaluation of Thrombocytopenia #Diagnosis #Hematology #Thrombocytopenia #Workup #Algorithm #Ddxof
Algorithm for the Evaluation ... Thrombocytopenia #Diagnosis ... #Hematology #Thrombocytopenia ... #Workup #Algorithm ... #Ddxof
Algorithm for the Evaluation and Management of Sickle Cell Crises Clinical Manifestations and Management #Diagnosis #Management #Hematology #SickleCell
Algorithm for the Evaluation ... Management #Diagnosis ... #Management #Hematology ... Manifestations #Workup ... #Algorithm #Ddxof
Approach to Thrombocytosis - Elevated Platelet Count - Differential Diagnosis Algorithm Peripheral Smear concerning for malignancy?
→ Refer to hematology ... for workup, including ... Vasculitides, IBD, Celiac ... disease, Kawasaki ... #Algorithm #hematology
Causes of Thrombocytopenia and Platelet Disorders - Differential Diagnosis and Workup History: - Prior platelet count, family
- Differential Diagnosis ... and Workup History ... cases: INR/PT, aPTT ... - Bone marrow evaluation ... #hematology
Systemic Sclerosis (Scleroderma) Multi-system autoimmune disease characterized by vasculopathy and progressive fibrosis of skin and internal organs 3
autoimmune disease ... interstitial lung disease ... Scleroderma #SSc #rheumatology ... #diagnosis #signs ... symptoms #testing #workup
Systemic Lupus Erythematosus (SLE) - Diagnosis and Management Summary • Epidemiology: 10-180/100,000, Typically Age 20-40, F:M
Systemic Lupus Erythematosus ... (SLE) - Diagnosis ... • Immunologic Workup ... : Chronic disease ... Management #Summary #rheumatology
Macrophage Activation Syndrome (MAS) Classified among the secondary or acquired forms of haemophagocytic lymphohistiocytosis (sHLH) What? A subset of
highly inflammatory disease ... Hypofibrinogenemia • ↑ PT ↑ PTT ... Activation #Syndrome #Diagnosis ... #Management #Hematology ... #Rheumatology
Causes of Abnormal PT and/or aPTT Prolonged Prothrombin Time (PT) 1. Acquired deficiency of FVII
Abnormal PT and/or aPTT ... Early liver disease ... associated with systemic ... Prolonged #Causes #diagnosis ... #differential #hematology
Maculopapular Rashes - THE ALGORITHMIC APPROACH The term maculopapule is a portmanteau, a combination of macule and
of the rash and systemic ... assessed for Lyme disease ... pathognomonic for SJS or EM ... require emergent evaluation ... #Diagnosis #Dermatology
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