17 results
diagnosis syndrome treatment disease classification criteria erythematosus lupus oncology sle systemic adultonset apml arthritis behcet behcets causes coagulation crisis cryofibrinogenemia
Adult-Onset Still's Disease Clinical triad: Fever, Arthralgia/arthritis, Skin rash ± odynophagia + Biological inflammation: Increased neutrophils, Hyperferritinemia, decreased
Still's Disease Clinical ... Pulmonary: pleural effusion ... • Ocular: uveitis ... Disease #diagnosis #management ... #treatment #rheumatology
Behcet's Syndrome - Diagnosis Diagnostic Criteria for Behget's Syndrome (International Study Group for Behget's Disease): • Recurrent,
genital ulcers - Ocular ... test Most Common Clinical ... erythema nodosum) • Ocular ... venous thromboses, arterial ... Diagnosis #criteria #rheumatology
Hepatopulmonary Syndrome - Diagnosis and Management Summary A defect in arterial oxygenation due to a gas exchange
Management Summary ... shunt (Type 2) Clinical ... cycles after right atrial ... SpO2 > 88% • Management ... #treatment #hepatology
EULAR/ACR Classification Criteria for Systemic Lupus Erythematosus Clinical Domains: • Constitutional domain: Fever • Cutaneous domain: Non-scarring
EULAR/ACR Classification ... Erythematosus Clinical ... or pericardial effusion ... low C4, Low C3 and ... Erythematosus #diagnosis #rheumatology
Differentiation Syndrome in APML Epidemiology: • Incidence: common in APL (2-48% depending on the study) • Triggers:
• Triggers: ATRA ... effusions, weight ... or 15 days of ATRA ... APML #diagnosis #management ... #hematology #oncology
Cryofibrinogenemia Summary Cryofibrinogenemia Epidemiology: • 40-70 years with a modest female predominance Cryofibrinogenemia: • The precipitation of a
Cryofibrinogenemia Clinical ... ocular thrombi ... Diagnosis: • + Clinical ... Cryofibrinogenemia #diagnosis #rheumatology ... #hematology
Behçet's Syndrome Systemic disease associated with inflammation of multiple organs, small-vessel vasculitis and large-vessel vasculopathy Epidemiology: • Young
association • M > F Clinical ... Vascular Disease: Arterial ... Behcet syndrome (Clinical ... Syndrome #diagnosis #management ... signs #symptoms #rheumatology
Rheumatoid Arthritis Summary Overview: chronic, inflammatory symmetric polyarthritis involving small joints of hands/feet, knees, shoulders Signs & Symptoms:
nodules, joint effusions ... Ultrasound Diagnosis: CLINICAL ... history, exam and ... Arthritis #diagnosis #management ... #rheumatology
Heparin Induced Thrombocytopenia (HIT) - Diagnosis and Management - GrepMed Handbook Presentation: • Plts ↓50% (nadir
Management - GrepMed ... venous (DVT/PE) or arterial ... Diagnosis: • Clinical ... non-heparin A/C if clinical ... #Treatment #Hematology
SAPHO Syndrome Summary What? SAPHO syndrome is a rare chronic inflammatory disorder of bone, joint, and skin characterized
Rheumatic pain Clinical ... , parts of the axial ... the collar bone ... SAPHO #Syndrome #Rheumatology ... #diagnosis #management
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