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diagnosis hematology treatment arteritis cap community cvid et gca giantcell hemeonc hemophagocytic hlh hypogammaglobulinemia immunodeficiency immunology lymphohistiocytosis pneumonia polycythemiavera pulmonary
Polycythemia Vera (PV) - Diagnosis and Management Summary Diagnostic Criteria: • Elevated hemoglobin and/or hematocrit AND •
Diagnosis and Management ... JAK2 mutation OR Abnormally ... , signs, and complications ... • Treatment algorithms ... with evidence of acquired
Common Variable Immunodeficiency (CVID) What? CVID: Immunodeficiency disorder with hypogammaglobulinemia -> increased infection risk secondary to impaired B-cell
- gastric and breast ... Chest CT: • Ground-glass ... severe community-acquired ... and M panel Management ... levels are within normal
Community Acquired Pneumonia (CAP) - Diagnosis and Management Pneumonia Signs/Symptoms: • Confusion/disorientation (LR + 1.9) • Cough
Diagnosis and Management ... Pneumonia Signs ... /Symptoms: • Confusion ... Uremia (blood urea ... CAP #Diagnosis #Management
Giant cell arteritis (GCA) Giant cell arteritis (GCA) definition: Most common systemic inflammatory vasculitis in older adults
definition: Most common ... systemic sx + signs ... 50 in GCA, but normal ... GCA #Temporal #Signs ... #Management
Essential Thrombocythemia (ET) ET is a chronic myeloproliferative neoplasm. Most cases are related to mutations that affect
Essential Thrombocythemia ... are usually near-normal ... thrombocytosis, only other commonly ... • Treatment algorithms ... hematology #diagnosis #management
Hemophagocytic Lymphohistiocytosis (HLH) High mortality without prompt recognition and management. HLH is a critical diagnostic consideration in
treatment are essential ... • Secondary (Acquired ... ) HLH: - Common ... Presentation • Common ... Signs and Symptoms
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