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management syndrome erythematosus lupus signs symptoms activation anisocoria arteritis behcet classification disease eularacr gca giantcell hematology horners macrophage mas physicalexam
SLICC SLE Diagnostic Criteria - Systemic Lupus Erythematosus Clinical and Immunologic Criteria CLINICAL CRITERIA - ACUTE CUTANEOUS LUPUS
SLICC SLE Diagnostic ... Erythematosus Clinical ... CLINICAL CRITERIA ... SEROSITIS - RENAL - NEUROLOGIC ... #Rheumatology #
EULAR/ACR Classification Criteria for Systemic Lupus Erythematosus Clinical Domains: • Constitutional domain: Fever • Cutaneous domain: Non-scarring
Erythematosus Clinical ... least 2 joints • Neurologic ... #SLE #Systemic ... Erythematosus #diagnosis ... #rheumatology
Macrophage Activation Syndrome (MAS) Classified among the secondary or acquired forms of haemophagocytic lymphohistiocytosis (sHLH) What? A subset of
develops on the background ... rash) • Heart, lung ... erythematosus [SLE ... Histopathologic criteria ... #Rheumatology
Horner's Syndrome on Physical Exam A 75yoF was referred in for facial swelling and eyelid changes 1
consistent with a diagnosis ... the apex of the lung ... Horners #Syndrome #clinical ... #video #ophthalmology ... #physicalexam #neurology
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 Behçet's Syndrome Systemic disease associated with inflammation of multiple organs, small-vessel vasculitis and large-vessel vasculopathy Epidemiology: • Young
skin injury) • Neurologic ... Oral aphthae : SLE ... • Arthritis: SLE ... inhibitors • Uveitis- Ophthalmology ... signs #symptoms #rheumatology
Giant cell arteritis (GCA) Giant cell arteritis (GCA) definition: Most common systemic inflammatory vasculitis in older adults
with systemic, neurologic ... Diagnosis = clinical ... day, followed by long ... them, but urgent rheumatology ... required +/- prompt ophthalmology
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