32 results
disease syndrome differential algorithm neurology causes classification erythematosus hemeonc hemophagocytic heparin hlh induced lupus lymphohistiocytosis oncology signs sle summary symptoms
Our approach to the diagnosis and initial management of patients with suspected HIT. Our approach is
and initial management ... laboratory tests ... and to adjust treatment ... #Diagnosis #Management ... #Hematology #HIT
Heparin Induced Thrombocytopenia (HIT) - Diagnosis and Management - GrepMed Handbook Presentation: • Plts ↓50% (nadir
) - Diagnosis and ... approach for post-test ... : Confirmatory test ... #Management #Treatment ... #Hematology #HemeOnc
Systemic Lupus Erythematosus - Summary Antinuclear (ANA) - 95% - Initial screening test Anti-dsDNA - 50% • Associated
Initial screening test ... severe disease Treatment ... #SLE #Summary #diagnosis ... #rheumatology # ... management
Adult-Onset Still's Disease Clinical triad: Fever, Arthralgia/arthritis, Skin rash ± odynophagia + Biological inflammation: Increased neutrophils, Hyperferritinemia, decreased
Differential Diaqnoses ... Coxsackie, CMV, EBV, HIV ... Stills #Disease #diagnosis ... #management #treatment ... #rheumatology
Leukostasis vs Tumor Lysis Syndrome Leukostasis: • Pathophysiology: Large, immature blasts and high WBC count cause hyperviscosity
priapism • Lab values ... organ damage • Treatment ... sudden death • Lab values ... Syndrome #TLS #diagnosis ... #management #hematology
CNS Manifestations of Systemic Lupus Erythematosus (SLE) Clinical Manifestations: Demyelinating Syndrome, Headache, Movement disorders, Seizure disorders, Aseptic
permeability Diagnosis ... Puncture, EEG Treatment ... #rheumatology # ... cerebritis #diagnosis ... #management #treatment
Kawasaki Disease (KD) - Diagnosis and Management Summary Kawasaki Disease (KD) is the most common vasculitis of
Disease (KD) - Diagnosis ... and Management ... , diarrhea • It ... KD #vasculitis #rheumatology ... #management #treatment
IgG4-Related Disease Clinical history: Man, 60 years, multiorgan involvement, unique or multiple inflammatory pseudotumor 4 phenotypes: •
with response to treatment ... specific laboratory tests ... #management #phenotypes ... #workup #treatment ... #rheumatology
Behçet's Syndrome Systemic disease associated with inflammation of multiple organs, small-vessel vasculitis and large-vessel vasculopathy Epidemiology: • Young
is a skin prick test ... Arthritis, AS Treatment ... • Nonsurgical abdominal ... #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
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