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management hematology differential signs treatment disease rheumatology workup abnormal agglutinin aids algorithm alkaline alp amyloid amyloidosis anemia associated barre behcet
Abnormal liver function tests algorithm. This figure details the initial response to abnormal liver blood tests.
symptoms/signs ... presence of metabolic syndrome ... Areas of diagnostic ... Abnormal #Algorithm #Hepatology ... #Differential #Diagnosis
Effects of Strokes by Location - Anterior vs Posterior Localization Anterior Circulation - MCA -
Artery #Strokes #Syndromes ... CVA #Territory #Symptoms ... #Diagnosis #Table ... GrepMed Recommended Text ... Comprehensive Review in Clinical
Causes of Thrombocytopenia and Platelet Disorders - Differential Diagnosis and Workup History: - Prior platelet count, family
- Differential Diagnosis ... K), H. pylori test ... (GI symptoms/endemic ... thyroid function test ... (CVID, WAS), (neurologic
Hemophagocytic Lymphohistiocytosis (HLH) Definition: Overwhelming clinical syndrome associated with excessive macrophage activation and cytokine storm due to
: Overwhelming clinical ... syndrome associated ... excessive macrophage activation ... HLH signs and symptoms ... lymph node, or liver
Behçet's Syndrome Systemic disease associated with inflammation of multiple organs, small-vessel vasculitis and large-vessel vasculopathy Epidemiology: • Young
association • M > F Clinical ... skin injury) • Neurologic ... meningitis), MCC CNS symptoms ... (Clinical Dx). ... #signs #symptoms
Cold Agglutinin Disease 3 Types of Cold Sensitive Antibodies: 1. Cold Agglutinins (CAD) 2. Donath-Landsteiner
Cold Agglutinin Syndrome ... Viral Infection Clinical ... Test: Donath-Landsteiner ... test #cold # ... hemolytic #anemia #hematology
Hepatopulmonary Syndrome - Diagnosis and Management Summary A defect in arterial oxygenation due to a gas exchange
Hepatopulmonary Syndrome ... shunt (Type 2) Clinical ... 10 minutes of rest ... resolution of symptoms ... #treatment #hepatology
Macrophage Activation Syndrome (MAS) Classified among the secondary or acquired forms of haemophagocytic lymphohistiocytosis (sHLH) What? A subset of
Macrophage Activation ... Clinical Presentation ... Fever is the main clinical ... function tests ... #Syndrome #Diagnosis
Inherited Non-hemolytic Disorders of Hyperbilirubinemia == Disorders of Conjugation == Gilbert Syndrome: • 5-10% of the population
of hemolysis or liver ... as jaundice on clinical ... examination; nonspecific symptoms ... Congenital #bilirubin #hepatology ... #diagnosis #gastroenterology
Amyloidosis - Summary Group of disorders associated with extracellular deposition of fibrils formed from low-molecular-weight proteins in
Clinical suspicion ... Amyloidosis Clinical ... : • Nephrotic syndrome ... Inflammation → Macrophage activation ... imaging of liver
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