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differential rheumatology management algorithm causes oncology photo rash cutaneous systemic treatment vasculitis signs skinrash erythematosus hepatology lupus symptoms anemia classification
Staphylococcal Scalded Skin Syndrome (SSSS) (aka Ritter disease) #Staphylococcal #Scalded #Skin #Syndrome #SSSS #Diagnosis #Pediatrics #Dermatology #Ritter
Syndrome (SSSS) ... #Syndrome #SSSS ... #Diagnosis #Pediatrics ... #Dermatology #Ritter ... #Disease #Peds
Vasculitis Involving the Skin - Differential Diagnosis Framework Primary: 50% Cutaneous Vasculitis: Leukocytoclastic Vasculitis Secondary: CTD: SLE, RA
- Differential Diagnosis ... Urticaria • Medium ... Vasculitis: • Behcet Disease ... • Cogan syndrome ... #dermatology #rheumatology
Skin Conditions Associated with Joint Pain Rash • Human parvovirus B19 infection Malar rash • SLE • Human parvovirus B19 infection •
infection • Lyme disease ... Antiphospholipid-antibody syndrome ... Sarcoidosis #dermatology ... #differential #diagnosis ... #rheumatology
Pruritus - Generalized Differential Diagnosis Algorithm - Systemic and Primary Causes == Primary Skin Lesions == Macules /
Generalized Differential Diagnosis ... Liver Function Tests ... Myelodisplastic syndrome ... Psychiatric Disease ... #generalized #dermatology
Cutaneous manifestations associated with myelodysplastic syndrome • Myeloid hemopathy with the most frequent skin lesions (20%)
most frequent skin ... appearing during the disease ... #differential #diagnosis ... #dermatology #oncology ... #clinical #skin
Vascular Lesions: Spider Angioma, Spider Vein, Cherry Angioma #Vascular #Spider #Angioma #Vein #Cherry #Comparison #Dermatology #Skin
Cherry #Comparison #Dermatology ... #Skin #Diagnosis ... #Clinical ** ... GrepMed Recommended Text
Dermatologic Manifestations of Granulomatosis with Polyangiitis (GPA) Skin involvement in granulomatosis with polyangiitis (GPA) is common and
Rarely dominate the clinical ... Differential Diagnosis ... • Goodpasture syndrome ... Polyangiitis #GPA #dermatology ... #rash #diagnosis
Behcet's Syndrome - Diagnosis Diagnostic Criteria for Behget's Syndrome (International Study Group for Behget's Disease): • Recurrent,
vasculitis - Skin ... Abnormal pathergy test ... Most Common Clinical ... oligoarticular, medium-large ... #disease #Diagnosis
Cutaneous Manifestations of Monoclonal Gammopathy • Extravascular lg Deposits: Systemic amyloidosis, Nodular amyloidosis, Macroglobulinoderma, Follicular hyperkeratotic
Cold agglutinin disease ... secretion: POEMS syndrome ... , Syndrome Schnitzler ... manifestations #dermatology ... #skin #clinical
Behçet's Syndrome Systemic disease associated with inflammation of multiple organs, small-vessel vasculitis and large-vessel vasculopathy Epidemiology: • Young
association • M > F Clinical ... Medium and large ... (Clinical Dx). ... (this is a skin ... signs #symptoms #rheumatology
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