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diagnosis hematology rheumatology syndrome clinical oncology table thrombocytopenic ttp acne activation anemia antinxp2 antinxp2dm aplastic ascorbicacid behcet causes classification coagulation
Purpuric Skin Lesions - Petechia/Purpura and Ecchymosis #Purpuric #Purpura #Petechia #Ecchymosis #Comparison #Dermatology #Skin #Diagnosis #Clinical
Purpuric Skin Lesions ... - Petechia/Purpura ... #Purpura #Petechia ... #Ecchymosis #Comparison ... #Dermatology #Skin
Thrombotic Microangiopathy - TTP VS HUS Big picture points : Often hard to differentiate the two entities,
distinction has HUGE treatment ... and first-line treatment ... thrombocytopenic #purpura ... thrombocytopenia #Comparison ... Diagnosis #Table #Hematology
Treatment of Thrombotic Thrombocytopenic Purpura (TTP) Diagnosis of TTP: • Rare and severe, ADAMTS13 deficiency • Autoimmune
Treatment of Thrombotic ... Thrombocytopenic Purpura ... Thrombocytopenic #Purpura ... #management #treatment ... #rheumatology #hematology
Mild Acne Treatment - Comedones (black/whiteheads), +/- few pustules 1. Benzoyl Peroxide (BP) 2. Topical Retinoid
Mild Acne Treatment ... of some larger lesions ... ambcarerx #Acne #Treatment ... #Mild #Management ... #Pharmacology #Dermatology
Scurvy (Vitamin C Deficiency) - Diagnosis and Management Vitamin C is required for hydroxylation of proline residues
Diagnosis and Management ... • Petechia • Purpura ... • Petechiae, purpura ... vasculitis Treatment ... Nutrition #Diagnosis #Management
Disseminated Intravascular Coagulation (DIC) Overview Increased Clotting and Consumption of Clotting Factors Findings: • Bleeding • Recent history
Petechiae • Purpura ... Hemorrhagic bullae • Purpura ... + Bleeding Treatment ... diagnosis #causes #treatment ... #management #hematology
Behçet's Syndrome Systemic disease associated with inflammation of multiple organs, small-vessel vasculitis and large-vessel vasculopathy Epidemiology: • Young
• Urogenital Lesions ... ) • Cutaneous Lesions ... , palpable purpura ... Arthritis, AS Treatment ... Syndrome #diagnosis #management
Macrophage Activation Syndrome (MAS) Classified among the secondary or acquired forms of haemophagocytic lymphohistiocytosis (sHLH) What? A subset of
easy bruising to purpura ... (Petechial or purpuric ... Treatment: • Corticosteroids ... Syndrome #Diagnosis #Management ... #Hematology #Rheumatology
Scleroderma Like Conditions - Differential Diagnosis Eosinophilic Fasciitis: - Orange peel induration (peau d'orange) of proximal extremities
the mainstay of treatment ... planus-like skin lesions ... Differential #Diagnosis #comparison ... #table #dermatology
Aplastic Anemia - Overview Who? • M = F • 3 peaks: 1) Childhood 2) 15-25 years 3) >60 years What? • Aplastic anemia
: - Genetic lesions ... aplastic anemia Treatment ... Anemia #oncology #hematology ... #diagnosis #management
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