7 results
Amyotrophic Lateral Sclerosis (ALS) Summary
ALS: combination of the clinical examination finding of amyotrophy with the pathologic
Presentation: - Disease ... course of the disease ... diagnosis: months - Criteria ... : El Escorial criteria ... neurology #diagnosis #management
Evaluation of suspected incomplete Kawasaki Disease

1. AHA consensus recommendations
2. Infants ≤6 months old on day ≥7
incomplete Kawasaki Disease ... , elevation of ALT ... clinical and lab signs ... #Diagnosis #Peds ... Pediatrics #Kawasaki #Disease
Cryptogenic Organizing Pneumonia - Illness Script

PATHOPHYSIOLOGY: Unknown trigger, reversible inflammatory/fibroproliferative process. Polypoid fibroblastic aggregates that plug
Cryptogenic Organizing ... Males=Females SIGNS ... usually misdiagnosed as ... steroids for severe disease ... Pneumonia #diagnosis #management
Multiple Sclerosis - Summary

Multiple Sclerosis (MS) is an autoimmune-mediated neurodegenerative disease of the central nervous system
neurodegenerative disease ... syndromes such as ... • Lhermitte’s sign ... McDonald diagnostic criteria ... sclerosis #diagnosis #management
Polycythemia Vera (PV) - Diagnosis and Management Summary
Diagnostic Criteria:
 • Elevated hemoglobin and/or hematocrit AND
 •
Diagnosis and Management ... Summary Diagnostic Criteria ... present, symptoms, signs ... von Willebrand disease ... PV #Diagnosis #Management
Pheochromocytoma - Diagnosis and Management Summary
10 percent rule = 10% of pheochromocytomas are extra-adrenal, multiple, bilateral,
Symptoms and Signs ... common symptoms and signs ... leukocytosis, psychiatric ... certain drugs (such as ... Treatment • Operable disease
Hemophagocytic Lymphohistiocytosis (HLH)

High mortality without prompt recognition and management. HLH is a critical diagnostic consideration in
• In all patients ... ▪ Autoimmune diseases ... Presentation • Common Signs ... Diagnostic Criteria ... of 8 HLH-2004 criteria