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treatment disease symptoms syndrome arthritis cardiology differential hemophagocytic hlh lymphohistiocytosis summary vasculitis adultonset anomalous antinxp2 antinxp2dm arteritis behcet capillary cardiomyopathy
Total Anomalous Pulmonary Venous Return (TAPVR) • Introduction • Classification • Pathophysiology of TAPVR • Presentation
Total Anomalous Pulmonary ... Introduction • Classification ... PVO Present • Diagnosis ... Classic “snowman sign ... #peds #pediatrics
Classification and Clinical Features of JIA (Juvenile Idiopathic Arthritis) #Juvenile #Idiopathic #Arthritis #JIA #diagnosis #rheumatology #signs #symptoms
Classification and ... Clinical Features ... Arthritis #JIA #diagnosis ... #rheumatology # ... signs #symptoms
Adult-Onset Still's Disease Clinical triad: Fever, Arthralgia/arthritis, Skin rash ± odynophagia + Biological inflammation: Increased neutrophils, Hyperferritinemia, decreased
Still's Disease Clinical ... Differential Diaqnoses ... hepatitis • Pulmonary ... #management #treatment ... #rheumatology
Susac Syndrome - Clinical Triad - Central nervous system dysfunction - Branch retinal artery occlusion -
Susac Syndrome - Clinical ... disease flares - 2-year ... SusacSyndrome #Triad #Diagnosis ... #Management #Rheumatology
Cryofibrinogenemia Summary Cryofibrinogenemia Epidemiology: • 40-70 years with a modest female predominance Cryofibrinogenemia: • The precipitation of a
Cryofibrinogenemia Clinical ... thrombophlebitis, pulmonary ... : • + Clinical ... #rheumatology # ... hematology
Rheumatoid Arthritis Summary Overview: chronic, inflammatory symmetric polyarthritis involving small joints of hands/feet, knees, shoulders Signs & Symptoms:
knees, shoulders Signs ... • Ultrasound Diagnosis ... : CLINICAL DIAGNOSIS ... Rheumatoid #Arthritis #diagnosis ... #management #rheumatology
Hemophagocytic Lymphohistiocytosis (HLH) Definition: Overwhelming clinical syndrome associated with excessive macrophage activation and cytokine storm due to
: Overwhelming clinical ... : HLH signs and ... Diagnosis via genetic ... #management #treatment ... #hematology
Hemophagocytic Lymphohistiocytosis (HLH) Pathophysiology: Triggering factor (infection,...)→Activation of CD8 T cells (IFN-y) → Excessive activation of macrophages
accumulation of clinical ... Assessment • Clinical ... Nicolas Taar ... #management #treatment ... #summary #rheumatology
Sarcoidosis - Diagnosis and Management Summary Epidemiology 1) High incidence in Scandinavian countries (11-24 cases per 100,000 individuals
and Management ... renal failure Clinical ... Pulmonary: dyspnea ... acute sarcoidosis Pulmonary ... #Management #Signs
Behçet's Syndrome Systemic disease associated with inflammation of multiple organs, small-vessel vasculitis and large-vessel vasculopathy Epidemiology: • Young
association • M > F Clinical ... Behcet syndrome (Clinical ... Giant retinal tears ... #management #signs ... #symptoms #rheumatology
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