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diagnosis rheumatology dermatology signs symptoms syndrome anemia antinxp2 antinxp2dm aplastic arteritis behcet dermatomyositis differential disease gca giantcell sapho temporal vasculitis
Behçet's Syndrome Systemic disease associated with inflammation of multiple organs, small-vessel vasculitis and large-vessel vasculopathy Epidemiology: • Young
response to local skin ... injury) • Neurologic ... test (this is a skin ... Syndrome #diagnosis #management ... signs #symptoms #rheumatology
SAPHO Syndrome Summary What? SAPHO syndrome is a rare chronic inflammatory disorder of bone, joint, and skin characterized
blisters containing pus ... lesions + Rheumatic ... Rule out other causes ... #diagnosis #management ... #Dermatology
Vasculitis - Differential Diagnosis Framework When to Consider Vasculitis: • Purpura, ischemic skin lesions • Mononeuritis multiplex • Hematuria, proteinuria,
lesions • Mononeuritis ... , neurologic, and ... cognitive impairment, neurologic ... tract, and often causes ... Differential #Diagnosis #Rheumatology
Aplastic Anemia - Overview Who? • M = F • 3 peaks: 1) Childhood 2) 15-25 years 3) >60 years What? • Aplastic anemia
Headaches • Pale skin ... and petechiae Causes ... : - Genetic lesions ... #hematology #diagnosis ... #management
Giant cell arteritis (GCA) Giant cell arteritis (GCA) definition: Most common systemic inflammatory vasculitis in older adults
with systemic, neurologic ... required due to skip ... lesions. ... identifies 85 to 95% of cases ... Symptoms #Diagnosis #Management
Anti-NXP-2 Dermatomyositis What? DM with generalized subcutaneous edema Pts have more myalgias, more severe weakness, and an increased prevalence
subcutaneous edema Pts ... have typical DM skin ... lesions: antihelix ... Muscle atrophy may cause ... Dermatomyositis #diagnosis #management
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