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diagnosis management differential symptoms chloride comparison crisis criticalcare features hematology hemeonc hemophagocytic histiocytosis hlh hypochloremia igg4 langerhans lch lymphohistiocytosis myelitis
Features of a Sickle Cell Crisis Sickle-cell disease - an autosomal recessive blood disorder. Characterized by red
Features of a Sickle ... blood vessels leading ... Crises can be precipitated ... The underlying pathophysiology ... #Signs #Symptoms
Shock Classification Types - Pathophysiology Comparison Obstructive Shock: • Obstructive shock is characterized by a blockage in
Shock Classification ... Types - Pathophysiology ... in blood flow caused ... Depends on the cause ... #Shock #Types #Pathophysiology
Hypochloremia - Differential Diagnosis Algorithm Cause - Decreased Intake: • Low salt in diet • Exclusive D5W
Differential Diagnosis Algorithm ... - Gitelman SIGNS ... smooth muscle cells ... gastrointestinal osmotic gradient ... #Pathophysiology
Sarcoidosis - Diagnosis and Management Summary Epidemiology 1) High incidence in Scandinavian countries (11-24 cases per 100,000 individuals
survival is 93-95% Pathophysiology ... : 1) T-cell dysfunction ... and increased B-cell ... failure Clinical Features ... Diagnosis #Management #Signs
Transverse Myelitis Overview Focal inflammatory disorder of the spinal cord resulting in rapid onset of weakness, sensory
bowel or bladder dysfunction ... monophasic Pathophysiology ... Alterations: - Sensory features ... • Bilateral signs ... Pleocytosis > 100 cells
Langerhans Cell Histiocytosis (LCH) Granulomatous Lesions comprising langerin-positive histiocytes and an inflammatory infiltrate can arise in virtually
, a type of dendritic ... various tissues, leading ... : LCH exhibits features ... • Endocrine Dysfunction ... marrow: Organ dysfunction
IGG-4 RELATED DISEASE WHAT? • A chronic, immune-mediated fibroinflammatory disease with tumefactive infiltration of IgG4+ plasma cells
- Organ dysfunction ... PATHOPHYSIOLOGY ... • Key Features ... • Pancreas: Type ... complement • Classification
Hemophagocytic Lymphohistiocytosis (HLH) High mortality without prompt recognition and management. HLH is a critical diagnostic consideration in
cytopenias and organ dysfunction ... hyperinflammatory syndrome caused ... Types of HLH • ... Presentation • Common Signs ... Pathophysiology
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