28 results
diagnosis management hematology infectiousdiseases differential disease oncology adultonset anemia aosd hemophagocytic hlh lymphohistiocytosis activation acute adult agglutinin aplastic apml bloodsmear
Fever Patterns - Differential Diagnosis Framework Continuous Fever: Temp > 38°C with only 1 degree fluctuation in 24
: • Still's disease ... Causes: • Still's ... • Hyper-IgD syndrome ... • Leptospirosis ... • Malaria • Leptospirosis
Adult-Onset Still's Disease (AOSD) Rare inflammatory disorder of unknown etiology, difficult to diagnose because of heterogenous presentation.
Adult-Onset Still's ... susceptibility, infectious ... : High spiking fever ... #AdultOnset #Stills ... Disease #AOSD #rheumatology
Adult-Onset Still's Disease Clinical triad: Fever, Arthralgia/arthritis, Skin rash ± odynophagia + Biological inflammation: Increased neutrophils, Hyperferritinemia, decreased
Adult-Onset Still's ... Clinical triad: Fever ... Diaqnoses: • Infectious ... diagnosis #management #treatment ... #rheumatology
Hantavirus Pathogen: Hantavirus - Rodents are the primary reservoir Transmission: • Shed in the urine, feces, saliva of
common route of infection ... Cardiopulmonary Syndrome ... • Prodrome: fever ... , chills, myalgias ... #microbiology #
Adult Onset Still's Disease Systemic inflammation with urticarial rash. Rash: • Nonpruritic, evanescent (correlates with time of
Adult Onset Still's ... Treatment - Mild ... : NSAIDS Treatment ... #Adult #onset #Stills ... AOSD #diagnosis #rheumatology
Macrophage Activation Syndrome (MAS) Classified among the secondary or acquired forms of haemophagocytic lymphohistiocytosis (sHLH) What? A subset of
• Adult-onset Still ... - Nonremitting fever ... SLE], AOSD) • Infection ... Treatment: • Corticosteroids ... #Rheumatology
Extra-articular and Other Conditions Associated with Joint Pain Eyes • Iritis or uveitis - Spondyloarthropathies, Sarcoidosis,
Bacterial or viral infection ... • Still's disease ... • Rheumatic fever ... Cardiomyopathies - Viral infection ... differential #diagnosis #rheumatology
Hemophagocytic Lymphohistiocytosis (HLH) Pathophysiology: Triggering factor (infection,...)→Activation of CD8 T cells (IFN-y) → Excessive activation of macrophages
• Clinical: fever ... +, Adult-onset Still ... Unknown cause Treatment ... diagnosis #management #treatment ... #summary #rheumatology
Disseminated Gonococcal Infection - Diagnosis and Management Summary Bacteremic spread of the Gram-negative diplococci Neisseria gonorrhoeae. History
Disseminated Gonococcal Infection ... Arthritis-Dermatitis syndrome ... : • Fever, chills ... Purulent Arthritis Syndrome ... Diagnosis #Management #Microbiology
Aplastic Anemia - Overview Who? • M = F • 3 peaks: 1) Childhood 2) 15-25 years 3) >60 years What? • Aplastic anemia
Presentation: • Fever ... Neutropenia - recurrent infections ... /fevers • Thrombocytopenia ... Idiopathic • Infections ... aplastic anemia Treatment
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