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diagnosis physicalexam video hematology slitlamp ocular treatment neurology krukenbergs spindle differential disease oncology ulcer ccdf central cloudy dystrophy eosinophilia eosinophils
Hypereosinophilia and Hypereosinophilic Syndrome • Secondary Hypereosinophilic Syndrome • Clinically Relevant HES Variants • When to
Hypereosinophilic Syndrome ... • Clinically ... Relevant HES Variants ... #HES #Hematology ... eosinophils #diagnosis #management
All About Horner's Syndrome Horner's syndrome, known as "oculosympathetic paresis" by people who don't have friends, is
Horner's syndrome ... in 1855 by Ed Horner ... Through his tireless ... efforts, he was ... #Overview #Ophthalmology
Behcet's Syndrome - Treatment Ulcers: • Treatment: Topical steroids • Prevention: Colchicine • Azathioprine for refractory disease Arthritis:
Behcet's Syndrome ... lesions • Derm referral ... • Early ophtho referral ... #Treatment #management ... #pharmacology #rheumatology
Corneal Ulcer: Marked generalized inflammation related to bacterial infection in this immunocompromised host. The cornea itself
Corneal Ulcer: Marked ... has become opaque ... UCSD Catalog of Clinical ... Images #Clinical ... #Ophthalmology
Keratoconus: Pathogenesis and Clinical Findings Genetics • Family history of keratoconus • Ehlers-Danlos syndrome • Down, Turner,
Pathogenesis and Clinical ... Ehlers-Danlos syndrome ... Turner, Marfan syndromes ... Bilateral, asymmetric corneal ... pathophysiology #ophthalmology
Giant cell arteritis (GCA) Giant cell arteritis (GCA) definition: Most common systemic inflammatory vasculitis in older adults
Diagnosis = clinical ... 95% of cases (Cornelia ... them, but urgent rheumatology ... required +/- prompt ophthalmology ... Symptoms #Diagnosis #Management
Supracondylar Elbow Fracture • Most common elbow fracture in children, peak age 5-7 • When looking at
posterior) and bone cortex ... ), compartment syndrome ... • ED Management ... No, if Type I; Yes ... XRay #Diagnosis #Management
Macrophage Activation Syndrome (MAS) Classified among the secondary or acquired forms of haemophagocytic lymphohistiocytosis (sHLH) What? A subset of
Macrophage Activation Syndrome ... Clinical Presentation ... Fever is the main clinical ... #Diagnosis #Management ... #Hematology #Rheumatology
Behçet's Syndrome Systemic disease associated with inflammation of multiple organs, small-vessel vasculitis and large-vessel vasculopathy Epidemiology: • Young
association • M > F Clinical ... (Clinical Dx). ... inhibitors • Uveitis- Ophthalmology ... #diagnosis #management ... signs #symptoms #rheumatology
Optic Neuritis - Diagnosis and Management • Epidemiology: Female (75%), 18-50 years, caucasian • Symptoms: Moderate visual
Diagnosis and Management ... - AQP4 : Yes ... Neuritis #Diagnosis #Management ... #treatment #rheumatology ... #ophthalmology
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