33 results
diagnosis rheumatology treatment syndrome dermatology hepatology idsa infections neurology opportunistic pharmacology prevention summary differential erythematosus hemeonc hemophagocytic hepatitis hlh igg4
Clinical diagnosis of Alcoholic Hepatitis (AH) • Onset of jaundice within prior 8 weeks • Ongoing
Clinical diagnosis ... Alcoholic Hepatitis (AH ... (Wilson disease ... Alcoholic #Hepatitis #AH ... #hepatology #criteria
VEXAS (Vacuoles, E1 enzyme, X-linked, Autoinflammatory, Somatic) Syndrome Clinical Syndrome: • Common Clinical Features: alveolitis, ear and
Somatic) Syndrome Clinical ... thromboembolic disease ... (MDS) Most met criteria ... for 1) hematologic ... and/or 2) Inflammatory
Macrophage Activation Syndrome (MAS) Classified among the secondary or acquired forms of haemophagocytic lymphohistiocytosis (sHLH) What? A subset of
release of pro-inflammatory ... Fever is the main clinical ... Histopathologic criteria ... Syndrome #Diagnosis #Management ... #Hematology #Rheumatology
IGG-4 RELATED DISEASE WHAT? • A chronic, immune-mediated fibroinflammatory disease with tumefactive infiltration of IgG4+ plasma cells
ureters • Aorta: Inflammatory ... • Essential Criteria ... : Clinical/radiologic ... 2019 ACR/EULAR Criteria ... #Rheumatology
IDSA Recommendations for Preventing and Treating Chagas Disease (American Trypanosomiasis) in HIV-AIDS Preventing Clinical Disease Indication: Individuals
HIV-AIDS Preventing Clinical ... Disease Indication ... and preventing clinical ... Prevention #Treatment #management ... opportunistic #infections #HIVAIDS
Common Variable Immunodeficiency (CVID) What? CVID: Immunodeficiency disorder with hypogammaglobulinemia -> increased infection risk secondary to impaired B-cell
to 8 years Clinical ... Gastrointestinal inflammatory ... and M panel Management ... hypogammaglobulinemia #immunology #hematology ... #diagnosis #management
Behçet's Syndrome Systemic disease associated with inflammation of multiple organs, small-vessel vasculitis and large-vessel vasculopathy Epidemiology: • Young
association • M > F Clinical ... (25-75%): Inflammatory ... Behcet syndrome (Clinical ... Syndrome #diagnosis #management ... signs #symptoms #rheumatology
Polycythemia Vera (PV) - Diagnosis and Management Summary Diagnostic Criteria: • Elevated hemoglobin and/or hematocrit AND •
Diagnosis and Management ... Summary Diagnostic Criteria ... for an unrelated indication ... von Willebrand disease ... Summary #treatment #hematology
The 6 C’s of Primary Sclerosing Cholangitis (PSC) PSC is a chronic, cholestatic, immune-mediated disease characterized by
there are many indications ... management. ... remain subject to clinical ... Cholangitis #diagnosis #management ... #summary #Hepatology
IgG4-Related Disease Clinical history: Man, 60 years, multiorgan involvement, unique or multiple inflammatory pseudotumor 4 phenotypes: •
IgG4-Related Disease ... Clinical history ... unique or multiple inflammatory ... IgG4 #Related #Disease ... #diagnosis #management
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