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diagnosis rheumatology table hematology oncology treatment acromegaly agep anemia aplastic behcet cutaneous dermatologic disease drug emergency endocrinology eosinophilia eosinophils erythroderma
Cutaneous manifestations associated with myelodysplastic syndrome • Myeloid hemopathy with the most frequent skin lesions (20%)
polymorphism • Satellite ... #differential # ... diagnosis #dermatology ... #oncology #clinical ... #skin
DRESS Syndrome vs SJS/TEN DRESS • Latency: 2-8 weeks • Rash: Morbilliform • Mucosal involvement: 50% have
DRESS Syndrome vs ... Prerenal azotemia • Skin ... #Syndrome #SJS ... #TEN #comparison ... #table #dermatology
Severe Drug Rashes - Comparison - DRESS | SJS/TEN | AGEP | Erythroderma DRESS - Onset:
Drug Rashes - Comparison ... >90% of total skin ... #Drug #Rashes #Comparison ... #Erythroderma #Dermatology ... #Emergency #Differential
Drug Reaction with Eosinophilia and Systemic Symptoms (DRESS) Syndrome Treatment Stop offending agents: • List as allergies
Systemic Symptoms (DRESS ... ) Syndrome Treatment ... , IVIG etc • Skin ... #Syndrome #Treatment ... #Management #dermatology
Drug Reaction with Eosinophilia and Systemic Symptoms (DRESS) Definition: • Severe adverse drug reaction, characterized by
Systemic Symptoms (DRESS ... characterized by extensive skin ... Skin involvement ... Resolution > 15 days Differentials ... #Syndrome #dermatology
Scleroderma Like Conditions - Differential Diagnosis Eosinophilic Fasciitis: - Orange peel induration (peau d'orange) of proximal extremities
Like Conditions - Differential ... large numbers of stellate ... #Scleroderma #Differential ... #Diagnosis #comparison ... #table #dermatology
Dermatologic Manifestations of Granulomatosis with Polyangiitis (GPA) Skin involvement in granulomatosis with polyangiitis (GPA) is common and
Dermatologic Manifestations ... Rarely dominate the clinical ... reticularis Differential ... • Goodpasture syndrome ... vasculitis #Dermatologic
SAPHO Syndrome Summary What? SAPHO syndrome is a rare chronic inflammatory disorder of bone, joint, and skin characterized
bone, joint, and skin ... Rheumatic pain Clinical ... Diagnosis: • A clinical ... Rheumatology #diagnosis #management ... #Dermatology
Behçet's Syndrome Systemic disease associated with inflammation of multiple organs, small-vessel vasculitis and large-vessel vasculopathy Epidemiology: • Young
association • M > F Clinical ... response to local skin ... (Clinical Dx). ... Behcet disease) Differential ... #diagnosis #management
Aplastic Anemia - Overview Who? • M = F • 3 peaks: 1) Childhood 2) 15-25 years 3) >60 years What? • Aplastic anemia
Constitutional Syndromes ... Aplastic Anemia Clinical ... Headaches • Pale skin ... Anemia #oncology #hematology ... #diagnosis #management
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