72 results
diagnosis symptoms dermatology management rheumatology differential peds syndrome complications rash vasculitis algorithm oncology treatment causes clinical primary ra workup activetb
Staphylococcal Scalded Skin Syndrome (SSSS) (aka Ritter disease) #Staphylococcal #Scalded #Skin #Syndrome #SSSS #Diagnosis #Pediatrics #Dermatology #Ritter
Staphylococcal Scalded Skin ... (aka Ritter disease ... SSSS #Diagnosis #Pediatrics ... #Dermatology #Ritter ... #Disease #Peds
Sarcoidosis Non-caseating granulomas (Composed of T-helper & inflammatory cells) Clinical: • Disease fatal in 10% of
& inflammatory cells ... Clinical: • Disease ... • Neurologic: Bell's ... neuropathies • Skin ... Diagnosis #Symptoms #Signs
Erythroderma - Diagnostic Algorithm. Pathophysiology: 1) Extensive cutaneous capillary dilation, results in widespread exfoliation of the
Pathophysiology: ... of germinative skin ... cells. ... Basophils/Histamine 4) Skin-homing ... #Dermatology #Rash
Systemic Sclerosis (Scleroderma) Multi-system autoimmune disease characterized by vasculopathy and progressive fibrosis of skin and internal organs 3
Multi-system autoimmune disease ... thickening Signs ... interstitial lung disease ... Scleroderma #SSc #rheumatology ... #diagnosis #signs
Maculopapular - Diagnostic Algorithm Pathophysiology: - Catch-all term with a wide range of potential pathophysiologic mechanisms and causative
Diagnostic Algorithm Pathophysiology ... - Pathophysiology ... Ill-appearing, vital sign ... sulfa-drug - Skin ... #Diagnosis #Dermatology
Combination of Skin Findings and Arthritis in Pediatrics Patient - Differential Diagnosis Malar rash: • A
Combination of Skin ... and Arthritis in Pediatrics ... migrans: • Target sign ... gabrieltalledop #dermatology ... diagnosis #peds #pediatrics
Giant Cell (Temporal) Arteritis: Pathogenesis and investigations Risk Factors: - Unclear environmental triggers (may be viral, not
yrs old; F>M Signs ... Anemia - Giant cells ... - Vasculitic skin ... Temporal #Arteritis #Pathophysiology ... #Diagnosis #Signs
Sickle Cell Disease - Pathophysiology of disease and complications Due to the deformed shape, HbS induces
Sickle Cell Disease ... - Pathophysiology ... the sickle red cells ... #Pathophysiology ... Complications #Hematology
Adult Onset Still's Disease - Yamaguchi Criteria Major criteria: - Fever >= 39C lasting >= 1 weeks
Onset Still's Disease ... weeks - Typical skin ... Leukocytosis >= 10,000 cells ... - Inflammatory disease ... #Major #Minor #Rheumatology
VEXAS (Vacuoles, E1 enzyme, X-linked, Autoinflammatory, Somatic) Syndrome Clinical Syndrome: • Common Clinical Features: alveolitis, ear and
nose chondritis, skin ... thromboembolic disease ... vasculitis • Hematologic ... criteria for 1) hematologic ... blood myeloid cells
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