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behcet cardiology chf clinical criticalcare differential foamed heartfailure hemophagocytic icu lymphohistiocytosis pharmacology sjogrens summary symptoms
Hemophagocytic Lymphohistiocytosis (HLH) Pathophysiology: Triggering factor (infection,...)→Activation of CD8 T cells (IFN-y) → Excessive activation of macrophages
) Pathophysiology ... Drugs, Unknown cause ... Treatment: • ... #management #treatment ... #summary #rheumatology
Behçet's Syndrome Systemic disease associated with inflammation of multiple organs, small-vessel vasculitis and large-vessel vasculopathy Epidemiology: • Young
common in Asia • HLA-B51 ... Arthritis, AS Treatment ... #diagnosis #management ... #signs #symptoms ... #rheumatology #
Sjogren's Syndrome Overview Epidemiology: • F > M: 9:1 • 5-6th Decades (can be any age) Autoimmune exocrinopathy multisystemic disease
Involvement: • Central ... Nephrogenic DI Hematologic ... Biologic: 2nd or 3rd line ... #Rheumatology # ... Diagnosis #Management
It is important to recognize Acute Decompensated Heart Failure (ADHF) as more than just simply a
pulmonary edema (“B-lines ... acute coronary syndrome ... the determined cause ... #algorithm #management ... #table #foamed
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