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diagnosis symptoms algorithm arteritis behcet giantcell hematology hemeonc hemophagocytic hlh incomplete kawasaki lymphohistiocytosis pediatrics syndrome temporal
Evaluation of suspected incomplete Kawasaki Disease 1. AHA consensus recommendations 2. Infants ≤6 months old on day ≥7
incomplete Kawasaki Disease ... Albumin ≤3.0 g/dL, anemia ... , treatment should ... clinical and lab signs ... #Diagnosis #Peds
Giant cell arteritis (GCA) Giant cell arteritis (GCA) definition: Most common systemic inflammatory vasculitis in older adults
with systemic, neurologic ... systemic complaints- anemia ... Biopsies remain positive ... Treatment of GCA ... them, but urgent rheumatology
Behçet's Syndrome Systemic disease associated with inflammation of multiple organs, small-vessel vasculitis and large-vessel vasculopathy Epidemiology: • Young
skin injury) • Neurologic ... Skin lesions • Positive ... Arthritis, AS Treatment ... #signs #symptoms ... #rheumatology #
Hemophagocytic Lymphohistiocytosis (HLH) High mortality without prompt recognition and management. HLH is a critical diagnostic consideration in
▪ Autoimmune diseases ... Presentation • Common Signs ... - Cytopenias (anemia ... molecular diagnosis: HScore ... #Hematology #HemeOnc
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