44 results
diagnosis treatment hematology syndrome differential nephrology causes hemophagocytic hlh lymphohistiocytosis oncology signs summary aosd classification comparison crisis encephalopathy gastroenterology hepatology
Cold Urticaria Prevalence - 0.05% in the population Disease onset - Mostly 2nd to 4th decades of life Causes
the population Disease ... trigger - Direct ... and duration of symptoms ... angioedema Other symptoms ... Urticaria #diagnosis #rheumatology
Leukostasis vs Tumor Lysis Syndrome Leukostasis: • Pathophysiology: Large, immature blasts and high WBC count cause hyperviscosity
Leukostasis: • Pathophysiology ... hyperviscosity syndrome • Triggers ... into serum • Triggers ... TLS #diagnosis #management ... #hematology
Dizziness and Vertigo Algorithm Presyncope: • Feels "faint" or like they are going to "pass out" •
"pass out" • Symptoms ... may be triggered ... spinning" • Symptoms ... differential #diagnosis #neurology ... #management
Pott's Disease in Tuberculosis - Diagnosis and Management Summary Epidemiology: - Typically from TB endemic areas -
Pott's Disease in ... Diagnosis and Management ... Clinical Signs/Symptoms ... decreased reflexes Pathophysiology ... CMC_IM #Potts #Disease
Migraine Treatment Overview • What is a Migraine? • Pathophysiology • Common Migraine Triggers • Diagnosis
• Pathophysiology ... Common Migraine Triggers ... Migraine #Treatment #management ... #prophylaxis #neurology
CNS Manifestations of Systemic Lupus Erythematosus (SLE) Clinical Manifestations: Demyelinating Syndrome, Headache, Movement disorders, Seizure disorders, Aseptic
Cerebrovascular Disease ... , PRES Pathophysiology ... Erythematosus #SLE #CNS #neurology ... #rheumatology # ... cerebritis #diagnosis #management
Gastroesophageal Reflux Disease (GERD) - Summary GERD: Diagnosis • Heartburn (substernal burning sensation) and acid regurgitation • Chest pain Extraesophageal
Gastroesophageal Reflux Disease ... and pulmonary symptoms ... reduction • Avoid “trigger ... Gastroesophageal #Reflux #Disease ... #diagnosis #management
Adult-Onset Still's Disease (AOSD) Rare inflammatory disorder of unknown etiology, difficult to diagnose because of heterogenous presentation.
Adult-Onset Still's Disease ... susceptibility, infectious triggers ... AdultOnset #Stills #Disease ... #AOSD #rheumatology ... #diagnosis #management
Behçet's Syndrome Systemic disease associated with inflammation of multiple organs, small-vessel vasculitis and large-vessel vasculopathy Epidemiology: • Young
skin injury) • Neurologic ... meningitis), MCC CNS symptoms ... Syndrome #diagnosis #management ... #signs #symptoms ... #rheumatology #
Features of a Sickle Cell Crisis Sickle-cell disease - an autosomal recessive blood disorder. Characterized by red
Sickle-cell disease ... Sickle cell disease ... The underlying pathophysiology ... Can be triggered ... Features #Signs #Symptoms
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