36 results
management rheumatology differential causes algorithm photo oncology secondary generalized signs symptoms syndrome chronic cll cutaneous dermatomyositis disorders erythematosus hemeonc leukemia
Purpuric Skin Lesions - Petechia/Purpura and Ecchymosis #Purpuric #Purpura #Petechia #Ecchymosis #Comparison #Dermatology #Skin #Diagnosis #Clinical
Purpuric Skin Lesions ... Petechia #Ecchymosis #Comparison ... #Dermatology #Skin ... #Diagnosis #Clinical
Nail Disorders secondary to Systemic Diseases Nail Fold Abnormality • SLE • Scleroderma • Dermatomyositis Koilonychia - Spoon-shaped
Disorders secondary to Systemic ... Iron deficiency anemia ... Discoloration • Medications ... #Secondary #dermatology ... #Differential #Diagnosis
Vascular Lesions: Spider Angioma, Spider Vein, Cherry Angioma #Vascular #Spider #Angioma #Vein #Cherry #Comparison #Dermatology #Skin
#Vein #Cherry #Comparison ... #Dermatology #Skin ... #Diagnosis #Clinical
Pruritus - Generalized Differential Diagnosis Algorithm - Systemic and Primary Causes == Primary Skin Lesions == Macules /
Generalized Differential Diagnosis ... Algorithm - Systemic ... renal failure/uremia ... #generalized #dermatology ... #Differential #Diagnosis
Clinical Features of Systemic Lupus (SLE) General: Fever (50%), Depression, Fatigue (75%), Weight loss (50%) Eye: Sjögrens (15%) Skin
Clinical Features ... Sjögrens (15%) Skin ... ) Blood (75%): Anemia ... signs #symptoms #diagnosis ... #rheumatology
Causes of Thrombocytopenia and Platelet Disorders - Differential Diagnosis and Workup History: - Prior platelet count, family
- Differential Diagnosis ... family history - Medications ... changes), high MCV ... anemia (vegan, ... Causes #Workup #hematology
Aplastic Anemia - Overview Who? • M = F • 3 peaks: 1) Childhood 2) 15-25 years 3) >60 years What? • Aplastic anemia
Clinical Presentation ... Headaches • Pale skin ... - Antithyroid medications ... #oncology #hematology ... #diagnosis #management
Macrophage Activation Syndrome (MAS) Classified among the secondary or acquired forms of haemophagocytic lymphohistiocytosis (sHLH) What? A subset of
fever syndromes Clinical ... Fever is the main clinical ... with leukopenia, anemia ... Activation #Syndrome #Diagnosis ... #Management #Hematology
Paraproteinemias Entities That Can Feature A Monoclonal Protein/M Component: • MM • WM • MGUS • MGCS • MGRS • Splenic Marginal Zone
Alpha & Mu) Skin ... thrombosis+Pulm HTN+skin ... (-) hemolytic anemia ... Paraproteinemias #Hematology ... #Differential #Diagnosis
Scleroderma Like Conditions - Differential Diagnosis Eosinophilic Fasciitis: - Orange peel induration (peau d'orange) of proximal extremities
- Differential Diagnosis ... treatment Nephrogenic Systemic ... #Differential #Diagnosis ... #comparison #table ... #dermatology
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