68 results
diagnosis management hematology differential infectiousdiseases neurology disease oncology dermatology acute algorithm causes classification idsa lupus microbiology photo american anemia associated
Approach to Thrombocytosis - Elevated Platelet Count - Differential Diagnosis Algorithm Peripheral Smear concerning for malignancy?
Rebound effect from treatment ... Vasculitides, IBD ... Kawasaki, Nephrotic syndrome ... Glucocorticoids, IL ... : Chronic infections
Myelodysplastic Syndrome (MD) - Diagnosis and Management Summary myelo (marrow) -dys- (abnormal) -plastic (shape) = funny-shaped cells
Myelodysplastic Syndrome ... diagnosis: 70 years old ... risk-stratification • Risks: infection ... only curative treatment ... #hematology #oncology
Adjuvant therapies in critical care: steroids to treat infectious diseases - Severe Community Acquired Pneumonia
Adjuvant therapies in critical ... steroids to treat infectious ... respiratory distress syndrome ... jirovecii pneumonia, id ... Pharmacology #Management #Treatment
BEE Syndromes - Non-inflammatory Causes Immune-mediated conditions affecting the Brain, Eye, and Ear Visual or auditory symptoms in
diagnosis and treatment ... • Enteroviral infections ... repair exonuclease 1 ... optic atrophy-1 ... MRI lesions and clinical
Acute Retroviral Syndrome Acute Retroviral Syndrome is the symptomatic presentation of acute human immunodeficiency virus infection •
Acute Retroviral Syndrome ... Acute Retroviral Syndrome ... Acute Retroviral Syndrome ... enzymes ↑ • Mild ... antibody test) Treatment
Macrophage Activation Syndrome (MAS) Classified among the secondary or acquired forms of haemophagocytic lymphohistiocytosis (sHLH) What? A subset of
-1 and IL-6, leading ... Clinical Presentation ... SLE], AOSD) • Infection ... Treatment: • Corticosteroids ... #Rheumatology
IDSA Algorithm for the Management of Purulent skin and soft tissue infections (SSTIs). Mild infection: for
Mild infection: ... Mild infection: ... erysipelas with no focus ... oral antibiotic treatment ... or those with clinical
Hemophagocytic Lymphohistiocytosis (HLH) Pathophysiology: Triggering factor (infection,...)→Activation of CD8 T cells (IFN-y) → Excessive activation of macrophages
cytokines (TNFa,lL1, IL6 ... accumulation of clinical ... Assessment • Clinical ... Unknown cause Treatment ... #summary #rheumatology
Common Variable Immunodeficiency (CVID) What? CVID: Immunodeficiency disorder with hypogammaglobulinemia -> increased infection risk secondary to impaired B-cell
• Affects 1:25,000 ... and 1:50,000 patients ... to 8 years Clinical ... : • Nephrotic syndrome ... (Epstein-Barr syndrome
Diagnosis of Cryoglobulinemia Vasculitis 1) Presence of cryoglobulin Circulating immunoglobulins that precipitate with cold temperature and dissolve
Vasculitis 1) ... not related to clinical ... Hyperviscosity syndrome ... (types II and Ill ... Vasculitis #Diagnosis #Rheumatology
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