81 results
diagnosis rheumatology treatment dermatology hepatology differential syndrome algorithm clinical photo workup lupus causes classification erythematosus primary sle vasculitis allergy cardiology
Systemic Lupus Erythematosus - Summary Antinuclear (ANA) - 95% - Initial screening test Anti-dsDNA - 50% • Associated
- Summary Antinuclear ... Initial screening test ... Erythematosus #SLE #Summary ... #diagnosis #rheumatology ... #management
Pyoderma Gangrenosum: Autoimmune disorder resulting in a vasculitis which causes slowly progressive ulceration of the skin.
a number of systemic ... diseases, it is ... inflammatory bowel disease ... Clinical #Photo #Dermatology ... #SkinRash #Pyoderma
Systemic Lupus Erythematosus (SLE) - Diagnosis and Management Summary • Epidemiology: 10-180/100,000, Typically Age 20-40, F:M
Systemic Lupus Erythematosus ... Summary • Epidemiology ... Evolution: Chronic disease ... #SLE #lupus #Systemic ... #Summary #rheumatology
Causes of Bleeding / Bruising - Differential Diagnosis Algorithm Thrombocytopenia - Quantitative Defect • Decreased Production •
• Increased Destruction ... ASA) • Renal Disease ... Vascular System ... TeIangiectasia Vascular System ... Algorithm #Causes #Hematology
End Stage Liver Disease (Cirrhosis) - Complications • Ascites • Esophageal Varices • Hepatic
End Stage Liver Disease ... Complications #diagnosis #management ... #summary #hepatology
Pruritus - Generalized Differential Diagnosis Algorithm - Systemic and Primary Causes == Primary Skin Lesions == Macules /
Diagnosis Algorithm - Systemic ... Liver Function Tests ... Cholestatic liver disease ... syndrome Psychiatric Disease ... #generalized #dermatology
Behcet's Syndrome - Treatment Ulcers: • Treatment: Topical steroids • Prevention: Colchicine • Azathioprine for refractory disease Arthritis:
ophtho referral • Systemic ... : • Systemic steroids ... : • Systemic steroids ... Syndrome #Treatment #management ... #pharmacology #rheumatology
Macrophage Activation Syndrome (MAS) Classified among the secondary or acquired forms of haemophagocytic lymphohistiocytosis (sHLH) What? A subset of
highly inflammatory disease ... of underlying disease ... Liver function tests ... Syndrome #Diagnosis #Management ... #Hematology #Rheumatology
Renal Cell Carcinoma (RCC) - Diagnosis and Management Summary Clinical features - Classic triad (flank pain, hematuria,
Diagnosis and Management ... Summary Clinical ... express Laboratory tests ... RCC #Diagnosis #Management ... #Summary
Adult-Onset Still's Disease Clinical triad: Fever, Arthralgia/arthritis, Skin rash ± odynophagia + Biological inflammation: Increased neutrophils, Hyperferritinemia, decreased
Adult-Onset Still's Disease ... solid cancers • Systemic ... diseases : other ... #diagnosis #management ... #treatment #rheumatology
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