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rheumatology diagnosis management algorithm guidelines differential polyangiitis anca gpa syndrome behcet classification dehydrogenase dermatologic dermatology egpa elevated eosinophilic laboratory lactate
Vasculitis Management - ACR/VF 2021 Guidelines for Treatment & Management • Giant Cell Arteritis (GCA) •
Vasculitis Management ... Guidelines for Treatment ... #Management #Treatment ... #ACR2021 #Guidelines ... #algorithm #rheumatology
Eosinophilic Granulomatosis with Polyangiitis (EGPA) - ANCA Vasculitis Management Algorithm - ACR/VF 2021 Guidelines • Active
Eosinophilic Granulomatosis ... alone in select pts ... #Management #Treatment ... #ACR2021 #Guidelines ... #algorithm #rheumatology
Dermatologic Manifestations of Granulomatosis with Polyangiitis (GPA) Skin involvement in granulomatosis with polyangiitis (GPA) is common and
commonly through its ... • Pauci-immune vasculitis ... vasculitis (inflamed ... Polyangiitis #GPA #dermatology ... rash #diagnosis #rheumatology
Granulomatosis with Polyangiitis (GPA) and Microscopic Polyangiitis (MPA) - ANCA Vasculitis Management Algorithm - ACR/VF 2021
Granulomatosis with ... Polyangiitis (MPA) - ANCA Vasculitis ... #Management #Treatment ... #ACR2021 #Guidelines ... #algorithm #rheumatology
Polyarteritis Nodosa (PAN) - Vasculitis Management Algorithm - ACR/VF 2021 Guidelines • Severe Disease → Remission
Nodosa (PAN) - Vasculitis ... • Non-Severe Disease ... #Management #Treatment ... #ACR2021 #Guidelines ... #algorithm #rheumatology
Vasculitis - Differential Diagnosis Framework When to Consider Vasculitis: • Purpura, ischemic skin lesions • Mononeuritis multiplex • Hematuria, proteinuria,
(GRANULOMATOUS ... /hr • Biopsy: Granulomatous ... May develop in pts ... chorioretinitis, CNS ... Differential #Diagnosis #Rheumatology
Vasculitis and Vasculitides - Differential Diagnosis Framework When to Consider Vasculitis: • Purpura, ischemic skin lesions •
glomerulonephritis - Granulomatous ... (Granulomatous ... disease): • Takayasu ... • ANA (Suggest CTD ... differential #diagnosis #rheumatology
Behçet's Syndrome Systemic disease associated with inflammation of multiple organs, small-vessel vasculitis and large-vessel vasculopathy Epidemiology: • Young
, small-vessel vasculitis ... panuveitis, retinal vasculitis ... MCC-small vessel vasculitis ... Arthritis, AS Treatment ... signs #symptoms #rheumatology
Elevated Lactate Dehydrogenase (LDH) - Differential Diagnosis Framework LDH is a cytoplasmic enzyme present in tissues throughout
Periodic paralyses CNS ... cardiovascular surgery ... tumor burden) Vasculitis ... • Eosinophilic granulomatosis ... polyangiitis • Granulomatosis
Sjogren's Syndrome Overview Epidemiology: • F > M: 9:1 • 5-6th Decades (can be any age) Autoimmune exocrinopathy multisystemic disease
) • Cutaneous vasculitis ... Nephrogenic DI Hematologic ... : 2% Systemic Vasculitis ... Adenocarcinoma Treatment ... Sjogrens #Syndrome #Rheumatology
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