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diagnosis management hematology syndrome gca acr2021 disease giantcell guidelines lupus vasculitis comparison druginduced hemophagocytic heparin hit hlh induced lymphohistiocytosis signs
Vasculitis Management - ACR/VF 2021 Guidelines for Treatment & Management • Giant Cell Arteritis (GCA) •
Guidelines for Treatment ... • Giant Cell Arteritis ... • Takayasu's arteritis ... ACR2021 #Guidelines #algorithm ... #rheumatology
Clinical Disease Characteristics and Suggested Algorithm for Diagnostic Evaluation of Patients With Symptoms of Polymyalgia Rheumatica #Diagnosis
Clinical Disease ... and Suggested Algorithm ... #Diagnosis #Rheumatology ... #Algorithm #GCA ... GiantCell #Temporal #Arteritis
Giant Cell Arteritis (GCA) - Vasculitis Management Algorithm - ACR/VF 2021 Guidelines • Visual Symptoms/Loss or
Giant Cell Arteritis ... Vasculitis Management Algorithm ... Vasculitis #Management #Treatment ... ACR2021 #Guidelines #algorithm ... #rheumatology
Telescoping Fingers on Physical Exam A 69-year-old woman with rheumatoid arthritis presented for the treatment of severe
with rheumatoid arthritis ... presented for the treatment ... RheumatoidArthritis #Clinical ... #Video #Rheumatology
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 Macrophage Activation Syndrome (MAS) Classified among the secondary or acquired forms of haemophagocytic lymphohistiocytosis (sHLH) What? A subset of
Macrophage Activation ... fever syndromes Clinical ... Fever is the main clinical ... Treatment: • Corticosteroids ... #Rheumatology
Hypereosinophilia and Hypereosinophilic Syndrome • Secondary Hypereosinophilic Syndrome • Clinically Relevant HES Variants • When to
Hypereosinophilic Syndrome • Clinically ... Diagnosis and Treatment ... Algorithm Matthew ... Syndrome #HES #Hematology ... diagnosis #management #algorithm
Anterior ischemic optic neuropathy (AION) - Recognition of giant cell arteritis (GCA) 1) Is visual loss caused
of giant cell arteritis ... posterior ciliary arteries ... Clinical manifestations ... GiantCellArteritis #GCA #Rheumatology ... Ophthalmology #Diagnosis #Algorithm
Hemophagocytic Lymphohistiocytosis (HLH) Pathophysiology: Triggering factor (infection,...)→Activation of CD8 T cells (IFN-y) → Excessive activation of macrophages
→Activation of CD8 ... IFN-y) → Excessive activation ... accumulation of clinical ... Assessment • Clinical ... #summary #rheumatology
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 ... SLE, Reactive arthritis ... , AS Treatment: ... signs #symptoms #rheumatology
Adult-Onset Still's Disease Clinical triad: Fever, Arthralgia/arthritis, Skin rash ± odynophagia + Biological inflammation: Increased neutrophils, Hyperferritinemia, decreased
Still's Disease Clinical ... Fever, Arthralgia/arthritis ... diagnosis #management #treatment ... #rheumatology
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