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rheumatology dermatology differential clinical comparison treatment photo algorithm cardiology lupus summary syndrome aosd causes criticalcare cutaneous erythematosus fingernail lines medications
Summary of Coagulation Deficiencies Inherited: • Hemophilia A - Deficiency of Factor VIII • Hemophilia B -
of Factor IX Acquired ... Acute DIC - Septic shock ... Deficiencies #Summary #table ... #comparison #diagnosis ... #hematology #deficiency
Nail Findings & Associated Conditions Change in color, texture, or shape can be harmless, but may suggest
texture, or shape can ... an underlying systemic ... disease ... #differential #diagnosis ... #table #lines
Nail Findings & Associated Conditions Change in color, texture, or shape can be harmless, but may suggest
texture, or shape can ... an underlying systemic ... disease ... #differential #diagnosis ... #table #lines
Systemic Lupus Erythematosus (SLE) - Diagnosis and Management Summary • Epidemiology: 10-180/100,000, Typically Age 20-40, F:M
Systemic Lupus Erythematosus ... (SLE) - Diagnosis ... Manifestations: - CRP ... Evolution: Chronic disease ... #rheumatology
Pulmonary Arterial Catheterization – Use and Interpretation: -Pulmonary arterial catheterization (PAC) has never been shown to improve
or the type of shock ... obtained by PAC can ... acute valvular disease ... cardiac index) -systemic ... #Differential #Table
Common Variable Immunodeficiency (CVID) What? CVID: Immunodeficiency disorder with hypogammaglobulinemia -> increased infection risk secondary to impaired B-cell
-> 40 years • Can ... severe community-acquired ... hemolytic anemia) • Systemic ... hypogammaglobulinemia #immunology #hematology ... #diagnosis #management
Paraproteinemias Entities That Can Feature A Monoclonal Protein/M Component: • MM • WM • MGUS • MGCS • MGRS • Splenic Marginal Zone
• Heavy Chain disease ... angioedema • vWD • acquired ... Sneddon-Wilkinson disease ... Paraproteinemias #Hematology ... #Differential #Diagnosis
Macrophage Activation Syndrome (MAS) Classified among the secondary or acquired forms of haemophagocytic lymphohistiocytosis (sHLH) What? A subset of
the secondary or acquired ... highly inflammatory disease ... Activation #Syndrome #Diagnosis ... #Management #Hematology ... #Rheumatology
Adult-Onset Still's Disease (AOSD) Rare inflammatory disorder of unknown etiology, difficult to diagnose because of heterogenous presentation.
Adult-Onset Still's Disease ... episode (30%) Systemic ... AOSD: high fever, CRP ... #AOSD #rheumatology ... #diagnosis #management
Antinuclear antibodies and Systemic lupus Anti-dsDNA 60-80% Association with disease activity (when with Farr assay) and lupus nephritis. Can
antibodies and Systemic ... Can also be measured ... erythematosus #diagnosis ... #rheumatology # ... table #ANA
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