29 results
differential hematology treatment neurology rheumatology oncology summary causes hepatology inflammatory signs abnormal activation allergy anemia antibiotics aplastic barre behcet cancer
Hypocalcemia - Diagnosis and Management PTH Independent (↑ PTH) • LOW VIT D -
Hypocalcemia - Diagnosis ... and Management ... , Kidney Disease ... Syndrome - ... #differential #algorithm
Abnormal liver function tests algorithm. This figure details the initial response to abnormal liver blood tests.
function tests algorithm ... symptoms/signs ... presence of metabolic syndrome ... alcohol-related liver disease ... LFTs #Abnormal #Algorithm
Pott's Disease in Tuberculosis - Diagnosis and Management Summary Epidemiology: - Typically from TB endemic areas -
Pott's Disease in ... and Management ... extrapulmonary cases Clinical ... of bacilli to bone ... CMC_IM #Potts #Disease
SAPHO Syndrome Summary What? SAPHO syndrome is a rare chronic inflammatory disorder of bone, joint, and skin characterized
Rheumatic pain Clinical ... : • A clinical ... diagnosis • Rule ... osteoarticular and skin disease ... #management #Dermatology
Renal Cell Carcinoma (RCC) - Diagnosis and Management Summary Clinical features - Classic triad (flank pain, hematuria,
Carcinoma (RCC) - Diagnosis ... and Management ... Summary Clinical ... Budd Chiari syndrome ... Symptoms of metastatic
Behçet's Syndrome Systemic disease associated with inflammation of multiple organs, small-vessel vasculitis and large-vessel vasculopathy Epidemiology: • Young
association • M > F Clinical ... meningitis), MCC CNS symptoms ... (Clinical Dx). ... #diagnosis #management ... #signs #symptoms
Restrictive Cardiomyopathy - Diagnosis and Causes Clinical: Dyspnea, Exercise Intolerance, ↑ "Right Sided-Symptoms" (ascites, hepatomegaly, ↑↑peripheral edema) Physical
Cardiomyopathy - Diagnosis ... and Causes Clinical ... ↑ "Right Sided-Symptoms ... Hyper-eosinophilc Syndrome ... differential #cardiology #algorithm
Polycythemia Vera (PV) - Diagnosis and Management Summary Diagnostic Criteria: • Elevated hemoglobin and/or hematocrit AND •
and Management ... Hypercellular bone ... • Treatment algorithms ... von Willebrand disease ... #Management #Summary
Aplastic Anemia - Overview Who? • M = F • 3 peaks: 1) Childhood 2) 15-25 years 3) >60 years What? • Aplastic anemia
= Hypocellular bone ... Aplastic Anemia Clinical ... • Improve the symptoms ... oncology #hematology #diagnosis ... #management
Hemophagocytic Lymphohistiocytosis (HLH) Definition: Overwhelming clinical syndrome associated with excessive macrophage activation and cytokine storm due to
: Overwhelming clinical ... syndrome associated ... age, however the disease ... HLH signs and symptoms ... Hemophagocytosis in bone
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