17 results
Amyloidosis - Summary
Group of disorders associated with extracellular deposition of fibrils formed from low-molecular-weight proteins in
Clinical suspicion ... : • Nephrotic syndrome ... Persistent pleural effusions ... Testing: • EKG • Echocardiogram ... disproportionate atrial
Amyloidosis on POCUS Echocardiogram - Subcostal 4 Chamber (S4C)
Pt with systemic AL amyloidosis presents with 1
Echocardiogram ... wall thickening and ... biatrial enlargement ... large pericardial effusion ... Cardiac #POCUS #clinical
Amyloidosis on POCUS Echocardiogram - Parasternal short axis (PSAX)
Pt with systemic AL amyloidosis presents with 1
Echocardiogram ... wall thickening and ... biatrial enlargement ... large pericardial effusion ... Cardiac #POCUS #clinical
Amyloidosis on POCUS Echocardiogram - Apical 4 Chamber (A4C)
Pt with systemic AL amyloidosis presents with 1
Echocardiogram ... wall thickening and ... biatrial enlargement ... large pericardial effusion ... Cardiac #POCUS #clinical
Amyloidosis on POCUS Echocardiogram - Parasternal long axis (PLAX)
Pt with systemic AL amyloidosis presents with 1
Echocardiogram ... wall thickening and ... biatrial enlargement ... large pericardial effusion ... Cardiac #POCUS #clinical
Hepatopulmonary Syndrome - Diagnosis and Management Summary
A defect in arterial oxygenation due to a gas exchange
Hepatopulmonary Syndrome ... Management Summary ... shunt (Type 2) Clinical ... cycles after right atrial ... hepatopulmonary #syndrome
Renal Cell Carcinoma (RCC) - Diagnosis and Management Summary
Clinical features - Classic triad (flank pain, hematuria,
Management Summary ... Clinical features ... Secondary Amyloidosis ... Budd Chiari syndrome ... RCC #Diagnosis #Management
Behçet's Syndrome
Systemic disease associated with inflammation of multiple organs, small-vessel vasculitis and large-vessel vasculopathy
Epidemiology:
 • Young
association • M > F Clinical ... ulceration • Ocular ... Vascular Disease: Arterial ... (Clinical Dx). ... #diagnosis #management
Antiphospholipid Syndrome (APS)
APS is a rare autoimmune disorder characterized by recurring blood clots resulting from antibodies
Antiphospholipid Syndrome ... at least: • 1 clinical ... presence of 1 clinical ... present Treatment (EULAR ... APS #diagnosis #management
Pulmonary Renal Syndromes - OnePager Summary
Autoimmune ANCA vasculitis (AAV): GPA (granulomatous with polyangiitis), EGPA (eosinophilic granulomatosis
Pulmonary Renal Syndromes ... o infection • Echocardiogram ... LVEF, pericardial effusion ... blood retum in serial ... differential #diagnosis #management