19 results
hematology differential syndrome blood disease hemeonc hemophagocytic heparin hlh induced lymphohistiocytosis oncology product reactions thrombocytopenia adultonset algorithm anemia antinxp2 antinxp2dm
Purpura - Differential Diagnosis Framework Non-blanchable, dark red to purple, hemorrhagic skin lesions that result from leakage
- Differential Diagnosis ... purple, hemorrhagic skin ... meningitidis - Varicella ... reactions • Erythema gangrenosum ... #hematology #rheumatology
Our approach to the diagnosis and initial management of patients with suspected HIT. Our approach is
approach to the diagnosis ... and initial management ... and to adjust treatment ... #Diagnosis #Management ... #Hematology #HIT
Heparin Induced Thrombocytopenia (HIT) - Diagnosis and Management - GrepMed Handbook Presentation: • Plts ↓50% (nadir
) - Diagnosis and ... arterial thrombosis, skin ... exposure (prevent skin ... #Management #Treatment ... #Hematology #HemeOnc
Pustular Skin Lesions - Differential Diagnosis Framework What are pustules? • Pustules < 5-10 mm + pus • Material
- Differential Diagnosis ... Varicella 3. ... Pyoderma gangrenosum ... #Differential #Diagnosis ... #Dermatology
Adult-Onset Still's Disease Clinical triad: Fever, Arthralgia/arthritis, Skin rash ± odynophagia + Biological inflammation: Increased neutrophils, Hyperferritinemia, decreased
Arthralgia/arthritis, Skin ... Differential Diaqnoses ... Coxsackie, CMV, EBV, HIV ... #management #treatment ... #rheumatology
Behçet's Syndrome Systemic disease associated with inflammation of multiple organs, small-vessel vasculitis and large-vessel vasculopathy Epidemiology: • Young
thrombophlebitis, pyoderma gangrenosum ... lesions, pyoderma gangrenosum ... Arthritis, AS Treatment ... #management #signs ... #symptoms #rheumatology
Hemophagocytic Lymphohistiocytosis (HLH) Definition: Overwhelming clinical syndrome associated with excessive macrophage activation and cytokine storm due to
It is rare in presentation ... It presents as an ... • Bicytopenia Treatment ... #management #treatment ... #hematology
SAPHO Syndrome Summary What? SAPHO syndrome is a rare chronic inflammatory disorder of bone, joint, and skin characterized
• A clinical diagnosis ... and lower jaw Treatment ... SAPHO #Syndrome #Rheumatology ... #diagnosis #management ... #Dermatology
Aplastic Anemia - Overview Who? • M = F • 3 peaks: 1) Childhood 2) 15-25 years 3) >60 years What? • Aplastic anemia
Headaches • Pale skin ... - HCV - HIV ... aplastic anemia Treatment ... Anemia #oncology #hematology ... #diagnosis #management
Disseminated Intravascular Coagulation (DIC) Overview Increased Clotting and Consumption of Clotting Factors Findings: • Bleeding • Recent history
deficiency) • HIT ... + Bleeding Treatment ... #Coagulation #diagnosis ... #causes #treatment ... #management #hematology
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