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diagnosis syndrome treatment blood causes disease infectiousdisease oncology product reactions signs symptoms activation adultonset antivirals apml arteritis behcet classification daas
Thrombocytosis - Differential Diagnosis Platelet Count > 450 Reactive: • Anemia/blood loss (Fe deficiency) • Infection/Sepsis • Non-infectious
Thrombocytosis - Differential ... deficiency) • Infection ... /Sepsis • Non-infectious ... (malignancy, rheumatologic ... causes #Platelets #hematology
Causes of Leukocytosis and Leukopenia - Differential Diagnosis • Eosinophilia (AEC > 500, hypereosinophilia > 1500):
and Leukopenia - Differential ... • Eosinopenia: Sepsis ... Lymphocytosis: Infection ... Leukocytosis #Leukopenia #Differential ... Diagnosis #causes #hematology
Rodent-associated Bacterial infections: Leptospirosis, Rat-bite fever, Tularemia, Plague #rodent #infections #leptospirosis #tularemia #ratbitefever #plague #rats #infectiousdisease #fever #differential #diagnosis #management #treatment #table
#rodent #infections ... plague #rats #infectiousdisease ... #fever #differential ... #diagnosis #management ... #treatment #table
Here is a quick guide on the common direct-acting antivirals (DAAs) for chronic hepatitis C virus
C virus (HCV) infection ... DAAs #Antivirals #table ... #medications #infectiousdisease ... #hepatology #HepC ... #HepatitisC #Management
Causes of Thrombocytopenia - Differential Diagnosis Framework Decreased Production: - Drugs (chemo, yang, sulfa, acetaminophen, NSAIDs, quinine,
Thrombocytopenia - Differential ... - Bacterial: Sepsis ... infiltration: malignancy, infection ... Thrombocytopenia #Differential ... Diagnosis #Framework #hematology
Adult-Onset Still's Disease Clinical triad: Fever, Arthralgia/arthritis, Skin rash ± odynophagia + Biological inflammation: Increased neutrophils, Hyperferritinemia, decreased
fraction < 20% Differential ... Diaqnoses: • Infectious ... Disease #diagnosis #management ... #treatment #rheumatology
Macrophage Activation Syndrome (MAS) Classified among the secondary or acquired forms of haemophagocytic lymphohistiocytosis (sHLH) What? A subset of
SLE], AOSD) • Infection ... brucellosis) • Sepsis ... Syndrome #Diagnosis #Management ... #Hematology #Rheumatology
Differentiation Syndrome in APML Epidemiology: • Incidence: common in APL (2-48% depending on the study) • Triggers:
initiation • Differential ... Diagnosis: Infection ... (sepsis), PE, DAH ... APML #diagnosis #management ... #hematology #oncology
Behçet's Syndrome Systemic disease associated with inflammation of multiple organs, small-vessel vasculitis and large-vessel vasculopathy Epidemiology: • Young
brainstem lesions, aseptic ... Behcet disease) Differential ... Syndrome #diagnosis #management ... signs #symptoms #rheumatology
SLE (Systemic Lupus Erythematosus) Suspect: Clinical evidence of (fatigue, rash, photosensitivity, inflammatory arthritis, weight loss, and fever) and
permanent alopecia Differential ... Non-autoimmune rheumatologic ... fibromyalgia) • Infections ... , APLA, PAC • Aseptic ... Erythematosus #Diagnosis #Rheumatology
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