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diagnosis syndrome oncology cardiology lupus algorithm criticalcare dermatology disease druginduced foamed hemeonc sle table activation adultonset anemia antinxp2 antinxp2dm aplastic
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 ... Disease #diagnosis #management ... #treatment #rheumatology
Systemic Lupus Erythematosus (SLE) - Diagnosis and Management Summary • Epidemiology: 10-180/100,000, Typically Age 20-40, F:M
Diagnosis and Management ... Age 20-40, F:M 9:1 ... • Clinical Manifestations ... life-threatening • Treatment ... #Summary #rheumatology
Rheumatoid Arthritis Summary Overview: chronic, inflammatory symmetric polyarthritis involving small joints of hands/feet, knees, shoulders Signs & Symptoms:
AM stiffness, >1 ... nodules, joint effusions ... Ultrasound Diagnosis: CLINICAL ... exam and imaging Treatment ... #rheumatology
Chronic Lymphocytic Leukemia (CLL) - Summary Overview: • Most common leukemia in adults • Disorder of
immunophenotype Clinical ... Manifestations: 1) ... Agents: 1) ... Leukemia #oncology #hematology ... hemeonc #diagnosis #management
Hepatopulmonary Syndrome - Diagnosis and Management Summary A defect in arterial oxygenation due to a gas exchange
Diagnosis and Management ... defect (Type 1) ... shunt (Type 2) Clinical ... ) on room air Treatment ... #treatment #hepatology
Susac Syndrome - Clinical Triad - Central nervous system dysfunction - Branch retinal artery occlusion -
Susac Syndrome - Clinical ... Therapeutic strategy 1. ... arterioles - Treatment ... Triad #Diagnosis #Management ... #Rheumatology
Differentiation Syndrome in APML Epidemiology: • Incidence: common in APL (2-48% depending on the study) • Triggers:
Triggers: ATRA treatment ... HoTN, edema and effusions ... symptoms, or> 1 ... APML #diagnosis #management ... #hematology #oncology
Macrophage Activation Syndrome (MAS) Classified among the secondary or acquired forms of haemophagocytic lymphohistiocytosis (sHLH) What? A subset of
cytokines, such as IL-1 ... Fever is the main clinical ... Treatment: • Corticosteroids ... Syndrome #Diagnosis #Management ... #Hematology #Rheumatology
Drug Induced Lupus vs SLE Drug Induced Lupus (DIL): • Epidemiology: -10% of all lupus cases, drug-dependent,
to 1:1 F:M • Clinical ... • Clinical Manifestations ... Usual therapeutic management ... comparison #table #rheumatology ... #diagnosis #management
Acute Recurrent Pericarditis = recurrence of Acute Pericarditis (AP) after free interval >4-6 weeks without symptoms, >1/4
without symptoms, >1/ ... onset, Abundant effusion ... Pericarditis #diagnosis #management ... #treatment #rheumatology ... #cardiology
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