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diagnosis differential treatment vasculitis causes classification coagulation dic hemophagocytic hlh intravascular lymphohistiocytosis polychondritis relapsing symptoms vasculitides
Behçet's Syndrome Systemic disease associated with inflammation of multiple organs, small-vessel vasculitis and large-vessel vasculopathy Epidemiology: • Young
(SVC/IVC occlusion ... syndrome (Clinical ... #Syndrome #diagnosis ... #management #signs ... #symptoms #rheumatology
Disseminated Intravascular Coagulation (DIC) Overview Increased Clotting and Consumption of Clotting Factors Findings: • Bleeding • Recent history
organ damage Clinical ... significant fibrin clot ... • Severe Liver Disease ... deficiency) • HIT ... #hematology
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 ... #hematology
Vasculitis and Vasculitides - Differential Diagnosis Framework When to Consider Vasculitis: • Purpura, ischemic skin lesions •
VASCULITIS: • Behçet ... reactions, and vaso-occlusive ... purpura: strong sign ... Cryoglobulins • HIV ... #rheumatology #
Vasculitis - Differential Diagnosis Framework When to Consider Vasculitis: • Purpura, ischemic skin lesions • Mononeuritis multiplex • Hematuria, proteinuria,
reactions, and vaso-occlusive ... purpura: Strong sign ... of shoulder and hip ... vasculitis • Behcet ... #Rheumatology
Relapsing Polychondritis What is it? Recurrent inflammation of the cartilage in the body (Autoimmune disorder) Who? • Most frequently: 40
the most common clinical ... Sarcoidosis • Behcet ... : • Clinical tests ... Polychondritis #rheumatology ... #diagnosis #management
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