15 results
diagnosis management differential hematology neurology dermatology sclerosis vasculitis acute adult als amyotrophic aosd autoimmune behcet chronic classification cll cord dermatosis
Polycythemia Vera (PV) - Diagnosis and Management Summary Diagnostic Criteria: • Elevated hemoglobin and/or hematocrit AND •
Summary Diagnostic Criteria ... , signs, and complications ... • Treatment algorithms ... von Willebrand disease ... #hematology
Multiple Sclerosis - Summary Multiple Sclerosis (MS) is an autoimmune-mediated neurodegenerative disease of the central nervous system
neurodegenerative disease ... central nervous system ... • Or brainstem syndromes ... Signs and symptoms ... McDonald diagnostic criteria
Evaluation of suspected incomplete Kawasaki Disease 1. AHA consensus recommendations 2. Infants ≤6 months old on day ≥7
incomplete Kawasaki Disease ... if evidence of systemic ... purposes of this algorithm ... echo is positive, treatment ... clinical and lab signs
Drug Reaction with Eosinophilia and Systemic Symptoms (DRESS) Definition: • Severe adverse drug reaction, characterized by
Eosinophilia and Systemic ... Criteria for Diagnosis ... different areas 3. ... : symptomatic treatment ... SinaiBmoreIMRes #DRESS #Syndrome
Behçet's Syndrome Systemic disease associated with inflammation of multiple organs, small-vessel vasculitis and large-vessel vasculopathy Epidemiology: • Young
Systemic disease ... meningitis), MCC CNS symptoms ... Arthritis, AS Treatment ... diagnosis #management #signs ... #symptoms #rheumatology
Adult Onset Still's Disease Systemic inflammation with urticarial rash. Rash: • Nonpruritic, evanescent (correlates with time of
Systemic inflammation ... the chest/trunk Symptoms ... weeks or longer 3. ... Treatment - Mild ... AOSD #diagnosis #rheumatology
Vasculitis and Vasculitides - Differential Diagnosis Framework When to Consider Vasculitis: • Purpura, ischemic skin lesions •
or proteinase 3 ... Symptoms (Sx) in ... purpura: strong sign ... are proteinase 3 ... differential #diagnosis #rheumatology
Diagnostic Criteria for Sweet Syndrome (Acute Febrile Neutrophilic Dermatosis) Major criteria 1. Abrupt onset of tender
for Sweet Syndrome ... inflammatory disease ... Excellent response to treatment ... with systemic corticosteroids ... #Diagnosis #Hematology
Chronic Lymphocytic Leukemia - Summary Cancer affecting lymphocytes/Mature B cell neoplasm • Lymphocytes accumulate in large numbers
with no early symptoms ... Physical Exam/Signs ... cells can indicate disease ... Agranulocytosis 3. ... microglobulin Treatment
Hemophagocytic Lymphohistiocytosis (HLH) Definition: Overwhelming clinical syndrome associated with excessive macrophage activation and cytokine storm due to
Overwhelming clinical syndrome ... affects infants < 3 ... age, however the disease ... Diagnosis: HLH signs ... and symptoms can
No results found for "3 pocus sign symptoms lachman criteria disease rheumatology algorithm systemic treatment syndrome"
Try removing search terms or sorting by relevance
Or Upload an image for you and others searching for #3 #pocus #sign #symptoms #lachman #criteria #disease #rheumatology #algorithm #systemic #treatment #syndrome