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management treatment differential rheumatology neurology hematology signs symptoms causes dermatology erythematosus lupus nephrology oncology sle systemic tb tuberculosis activetb allergy
Alzheimer's Disease - Summary • Epidemiology • Pathophysiology • Risk Factors • Presentation • Diagnosis •
Alzheimer's Disease ... - Summary • Epidemiology ... • Pathophysiology ... Treatment • Clinical ... #Summary #diagnosis
Type IV Hypersensitivity: Pathogenesis and clinical findings Definition: Unique because it is entirely T-Cell mediated; exposure to
Pathogenesis and clinical ... -> Particular CD4 ... Stevens-Johnson Syndrome ... HypersensitivityReaction #Allergy #Immunology ... #pathophysiology
Pott's Disease in Tuberculosis - Diagnosis and Management Summary Epidemiology: - Typically from TB endemic areas -
Pott's Disease in ... and Management Summary ... extrapulmonary cases Clinical ... decreased reflexes Pathophysiology ... intervention CMC
Systemic Lupus Erythematosus (SLE) - Diagnosis and Management Summary • Epidemiology: 10-180/100,000, Typically Age 20-40, F:M
Erythematosus (SLE) - Diagnosis ... and Management Summary ... 40, F:M 9:1 • Clinical ... Cytopenia: Common • Immunologic ... Evolution: Chronic disease
Secondary Causes of Hypertension - Differential Diagnosis Algorithm Hypertension - BP > 140/90 (>130/80 for DM) Hypertensive urgency
- Differential Diagnosis ... DM (visit 2), Diagnosis ... based on repeat clinic ... Renal Parenchymal Diseases ... Steroids (Cushing's, exogenous
Renal Cell Carcinoma (RCC) - Diagnosis and Management Summary Clinical features - Classic triad (flank pain, hematuria,
Carcinoma (RCC) - Diagnosis ... and Management Summary ... Clinical features ... Budd Chiari syndrome ... Hb levels and CBC
Multiple Myeloma Diagnosis and Management Summary Clinical Signs: • hyperCalcemia 28% (bone demineralization) • Renal disease 48%
Multiple Myeloma Diagnosis ... and Management Summary ... Clinical Signs ... demineralization) • Renal disease ... is also >100 CMC
Common Variable Immunodeficiency (CVID) What? CVID: Immunodeficiency disorder with hypogammaglobulinemia -> increased infection risk secondary to impaired B-cell
late adulthood • Diagnosis ... to 8 years Clinical ... : • Nephrotic syndrome ... (Epstein-Barr syndrome ... hypogammaglobulinemia #immunology
Schematic representation of the major sources of ammonia production and its excretory pathway (GI = gastrointestinal,
decompensated liver disease ... - Significant endogenous ... rare): - Reye syndrome ... deficiency #Ammonia #Pathophysiology ... #Differential #Diagnosis
Hemophagocytic Lymphohistiocytosis (HLH) Pathophysiology: Triggering factor (infection,...)→Activation of CD8 T cells (IFN-y) → Excessive activation of macrophages
Lymphohistiocytosis (HLH) Pathophysiology ... →Activation of CD8 ... accumulation of clinical ... Assessment • Clinical ... management #treatment #summary
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