23 results
rheumatology syndrome evaluation hepatology neurology summary treatment hemophagocytic hlh lymphohistiocytosis workup activation admission alcoholic alkaline alkaptonuria alp arthritis behcet blackurine
Algorithm for the Evaluation of Pediatric Head Trauma (PECARN) - Need for Head CT #Diagnosis #Management
Algorithm for the ... Need for Head CT #Diagnosis ... #Management #EM ... #Peds #Trauma # ... #Ddxof
Algorithm for the Evaluation and Management of Sickle Cell Crises Clinical Manifestations and Management #Diagnosis #Management #Hematology #SickleCell
Algorithm for the ... Sickle Cell Crises Clinical ... #Diagnosis #Management ... #Hematology #SickleCell ... #Ddxof
Evaluation and Management of Pediatric Fever #Diagnosis #Management #EM #Peds #Fever #Workup #Evaluation #Discharge #Admission #Algorithm
Pediatric Fever #Diagnosis ... #Management #EM ... #Peds #Fever #Workup ... Discharge #Admission #Algorithm ... #Ddxof
CNS Manifestations of Systemic Lupus Erythematosus (SLE) Clinical Manifestations: Demyelinating Syndrome, Headache, Movement disorders, Seizure disorders, Aseptic
CNS Manifestations ... Erythematosus (SLE) Clinical ... Cerebrovascular Disease ... , PRES Pathophysiology ... #management #treatment
Behçet's Syndrome Systemic disease associated with inflammation of multiple organs, small-vessel vasculitis and large-vessel vasculopathy Epidemiology: • Young
association • M > F Clinical ... basal ganglia, CNS ... Behcet syndrome (Clinical ... #management #signs ... #symptoms #rheumatology
Septic Arthritis - Diagnosis and Management Summary Clinical Exam: hot, swollen, pain with passive AND active ROM
and Management ... Summary Clinical ... necrosis, Lyme disease ... cervical, anal Cxs ... MH/CCF/CWRU EM
Macrophage Activation Syndrome (MAS) Classified among the secondary or acquired forms of haemophagocytic lymphohistiocytosis (sHLH) What? A subset of
fever syndromes Clinical ... Fever is the main clinical ... nervous system (CNS ... Activation #Syndrome #Diagnosis ... #Management #Hematology
Hemophagocytic Lymphohistiocytosis (HLH) Pathophysiology: Triggering factor (infection,...)→Activation of CD8 T cells (IFN-y) → Excessive activation of macrophages
Lymphohistiocytosis (HLH) Pathophysiology ... accumulation of clinical ... Assessment • Clinical ... • Autoimmune diseases ... #management #treatment
Sjogren's Syndrome Overview Epidemiology: • F > M: 9:1 • 5-6th Decades (can be any age) Autoimmune exocrinopathy multisystemic disease
salivary ducts Clinical ... nervous system (CNS ... • 8%-27% for CNS ... Nephrogenic DI Hematologic ... #Diagnosis #Management
Disseminated Intravascular Coagulation (DIC) Overview Increased Clotting and Consumption of Clotting Factors Findings: • Bleeding • Recent history
organ damage Clinical ... Thromboembolism (7%) • CNS ... • Severe Liver Disease ... #Coagulation #diagnosis ... #hematology
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