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classification differential rheumatology anemia aplastic behcet coagulation cryofibrinogenemia dic disseminated encephalopathy gastroenterology grading hemochromatosis hemophagocytic heparin hepatic hlh hodgkins hypertension
Our approach to the diagnosis and initial management of patients with suspected HIT. Our approach is
and to adjust treatment ... #Diagnosis #Management ... #Hematology #HIT ... #Heparin #Induced ... Thrombocytopenia #Algorithm
Algorithm regarding the diagnosis and treatment of Hereditary Hemochromatosis HH. Step 1: In the patient with
treatment of Hereditary ... of liver disease ... elevated iron indices ... #diagnosis #management ... #hepatology #gastroenterology
Cryofibrinogenemia Summary Cryofibrinogenemia Epidemiology: • 40-70 years with a modest female predominance Cryofibrinogenemia: • The precipitation of a
Cryofibrinogenemia Diagnosis ... cryoglobulins • Negative causes ... syndrome • Warfarin-induced ... Cryofibrinogenemia #diagnosis ... hematology
Portopulmonary Hypertension Presence of pulmonary arterial hypertension in a patient with portal hypertension No other obvious causes (chronic
other obvious causes ... , left heart disease ... m/s • Other signs ... pressure < 15mmHg TREATMENT ... #management #hepatology
Hepatic Encephalopathy - Diagnosis and Management Summary Definition: • Alteration in brain function manifested by neuropsychiatric symptoms
and Management ... of neurologic/cognitive ... over course of disease ... #Management #treatment ... #hepatology
Hemophagocytic Lymphohistiocytosis (HLH) Definition: Overwhelming clinical syndrome associated with excessive macrophage activation and cytokine storm due to
: Overwhelming clinical ... age, however the disease ... : HLH signs and ... #management #treatment ... #hematology
Disseminated Intravascular Coagulation (DIC) Overview Increased Clotting and Consumption of Clotting Factors Findings: • Bleeding • Recent history
organ damage Clinical ... deficiency) • HIT ... #Coagulation #diagnosis ... #causes #treatment ... #management #hematology
Behçet's Syndrome Systemic disease associated with inflammation of multiple organs, small-vessel vasculitis and large-vessel vasculopathy Epidemiology: • Young
association • M > F Clinical ... skin injury) • Neurologic ... (SVC/IVC occlusion ... Arthritis, AS Treatment ... #management #signs
Aplastic Anemia - Overview Who? • M = F • 3 peaks: 1) Childhood 2) 15-25 years 3) >60 years What? • Aplastic anemia
Aplastic Anemia Clinical ... and petechiae Causes ... Aplastic #Anemia #oncology ... #hematology #diagnosis ... #management
Rhabdomyolysis - Differential Diagnosis Framework and Management Summary Causes of Rhabdomyolysis: • Trauma: - Immobilization - Crush injury - Compartment
- Differential Diagnosis ... Dermatomyositis Clinical ... disease 2. ... #Management #causes ... #treatment #nephrology
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