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diagnosis management differential sclerosis adult als amyotrophic autoimmune cord disorders hematology hemeonc hemophagocytic hlh incomplete kawasaki lateral lymphohistiocytosis ms multiple
Adult Onset Still's Disease Systemic inflammation with urticarial rash. Rash: • Nonpruritic, evanescent (correlates with time of
Disease Systemic ... the chest/trunk Symptoms ... weeks or longer 3. ... #AOSD #diagnosis ... #rheumatology #
Multiple Sclerosis - Summary Multiple Sclerosis (MS) is an autoimmune-mediated neurodegenerative disease of the central nervous system
neurodegenerative disease ... central nervous system ... adults (mean age of onset ... Signs and symptoms ... McDonald diagnostic criteria
Evaluation of suspected incomplete Kawasaki Disease 1. AHA consensus recommendations 2. Infants ≤6 months old on day ≥7
incomplete Kawasaki Disease ... if evidence of systemic ... purposes of this algorithm ... 10 d of fever onset ... clinical and lab signs
Amyotrophic Lateral Sclerosis (ALS) Summary ALS: combination of the clinical examination finding of amyotrophy with the pathologic
of the nervous system ... ; (2) bulbar-onset ... fasciculations Common Symptoms ... more regions 3. ... Lateral #Sclerosis #neurology
Vasculitis - Differential Diagnosis Framework When to Consider Vasculitis: • Purpura, ischemic skin lesions • Mononeuritis multiplex • Hematuria, proteinuria,
Symptoms (SX) in ... purpura: Strong sign ... : • Onset is 50 ... or proteinase 3 ... Differential #Diagnosis #Rheumatology
Spinal Cord Disorders - Differential Diagnosis Framework Spinal cord neurological lesion: Clinical findings: • Symptoms and signs below
and signs below ... , Aspergillus 3. ... Sarcoidosis, Behcet disease ... , Scleroderma, Systemic ... differential #algorithm
Transverse Myelitis Overview Focal inflammatory disorder of the spinal cord resulting in rapid onset of weakness, sensory
resulting in rapid onset ... Diagnostic Criteria ... • Bilateral signs ... and/or symptoms ... diagnosis #management #neurology
Autoimmune Myositis - Differential Diagnosis Framework Inflammatory Myopathies: Commonly symmetric proximal muscle weakness, no substantial muscle pain
RP-ILD), dermato-rheumatologic ... papules and Gottron sign ... ) • Shawl sign ... ALS • Very slow onset ... • Conduction system
Hemophagocytic Lymphohistiocytosis (HLH) High mortality without prompt recognition and management. HLH is a critical diagnostic consideration in
of the immune system ... - Onset: Usually ... ▪ Autoimmune diseases ... Activation Syndrome) 3. ... and Symptoms:
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