25 results
Cholestatic Liver Disease: Primary Biliary Cirrhosis vs Primary Sclerosing Cholangitis

#pathophysiology #pbc #psc #hepatology #comparison
Primary Sclerosing Cholangitis ... #pathophysiology ... #pbc #psc #hepatology
The 6 C’s of Primary Sclerosing Cholangitis (PSC)
PSC is a chronic, cholestatic, immune-mediated disease characterized by
Primary Sclerosing Cholangitis ... (PSC) PSC is a ... • CHOLANGITIS ... remain subject to clinical ... Primary #Sclerosing #Cholangitis
Primary Biliary Cirrhosis (PBC) - Summary

PBC Epidemiology:
 • Female:Male 9:1
 • Common European descent
 • Age:
) - Summary PBC ... Pathophysiology ... nonsuppurative destructive cholangitis ... sclerosis group cholangitis ... #cholangitis #diagnosis
Type III Hypersensitivity: Pathogenesis and clinical findings
Definition: Small antigen-antibody complexes (produced from normal immune response to
Type III Hypersensitivity ... Pathogenesis and clinical ... sickness #TypeIII #Type3 ... Allergy #Immunology #pathophysiology
Type I Hypersensitivity: Pathogenesis and clinical findings
Definition: Production of lgE Antibodies that bind to harmless allergens
Type I Hypersensitivity ... Pathogenesis and clinical ... Anaphylaxis #TypeI ... #Type1 #HypersensitivityReaction ... Allergy #Immunology #pathophysiology
Type IV Hypersensitivity: Pathogenesis and clinical findings
Definition: Unique because it is entirely T-Cell mediated; exposure to
Type IV Hypersensitivity ... Pathogenesis and clinical ... ivy) #TypeIV #Type4 ... Allergy #Immunology #pathophysiology
Type II Hypersensitivity: Pathogenesis and clinical findings
Definition: When antigens bind to the body's cell surfaces, forming
Type II Hypersensitivity ... Pathogenesis and clinical ... cell surfaces #Type2 ... #Type2 #HypersensitivityReaction ... Allergy #Immunology #pathophysiology
Torsades de Pointes (TdP): Pathogenesis and Clinical Findings

Polymorphic ventricular tachycardia initiated by PVC in the setting
Pathogenesis and Clinical ... tachycardia initiated by PVC ... TdP #Diagnosis #pathophysiology
Gaucher Disease 

Pathophsiology
 • Lysosomal storage disorder
 • Deficiency of ß-glucocerebrosidase
• Accumulation of glucosylceramide in macrophages
Diagnosis
Gaucher Disease Pathophsiology ... in GBA1 gene Clinical ... Neurological involvement (type
Causes of Lactate Elevation, Lactic Acidosis - Differential Diagnosis

The most common causes of hyperlactatemia are usually:
are listed as Type ... of lactate as a clinical ... www.ncbi.nlm.nih.gov/pmc ... a multitude of clinical ... the appropriate clinical