40 results
diagnosis management rheumatology oncology lupus causes disease hepatology neurology sle algorithm dermatology erythematosus systemic anemia barre differential druginduced guillain hemeonc
Peripheral Blood Smear Analysis Hypochromia Megaloblastic Anemia Schistocytes: Microangiopathic hemolytic anemia (e.g. DIC, TTP, HUS) Microspherocytes: Autoimmune hemolytic anemia Sickled red
Peripheral Blood Smear Analysis ... #Blood #Smear #Analysis ... #hematology #microscopy ... #interpretation ... #clinical #anemia
Hypereosinophilia and Hypereosinophilic Syndrome • Secondary Hypereosinophilic Syndrome • Clinically Relevant HES Variants • When to
Hypereosinophilic Syndrome ... • Clinically ... suspect underlying hematologic ... Diagnosis and Treatment ... #HES #Hematology
Von Willebrand Disease - Most common inherited bleeding disorder Clinical • Easy bruising •
bleeding disorder Clinical ... GI. uterine) Laboratory ... factor VIII) Treatment ... Disease #Diagnosis #Hematology
Tumor Lysis Syndrome - Workup and Management Initial workup: BMP, Serum uric acid, LDH, Urine output, Consider
Tumor Lysis Syndrome ... creatinine ratio Laboratory ... of the above Treatment ... of Clinical TLS ... every 4-6 hrs • Dialysis
Classification of Tumor Lysis Syndrome (TLS) and Treatment of Metabolic Abnormalities of TLS Laboratory TLS: • Uric
of Tumor Lysis Syndrome ... (TLS) and Treatment ... Abnormalities of TLS Laboratory ... Calcium ≤ 7.0 mg/dL Clinical ... #TumorLysis #Syndrome
Our approach to the diagnosis and initial management of patients with suspected HIT. Our approach is
based primarily on clinical ... results of HIT laboratory ... Estimates of the clinical ... and to adjust treatment ... Diagnosis #Management #Hematology
SAPHO Syndrome Summary What? SAPHO syndrome is a rare chronic inflammatory disorder of bone, joint, and skin characterized
Rheumatic pain Clinical ... Diagnosis: • A clinical ... other etiology • Laboratory ... and lower jaw Treatment ... #Rheumatology #
Systemic Lupus Erythematosus (SLE) - Diagnosis and Management Summary • Epidemiology: 10-180/100,000, Typically Age 20-40, F:M
40, F:M 9:1 • Clinical ... versus DIL • Laboratory ... life-threatening • Treatment ... Management #Summary #rheumatology
Behçet's Syndrome Systemic disease associated with inflammation of multiple organs, small-vessel vasculitis and large-vessel vasculopathy Epidemiology: • Young
association • M > F Clinical ... pathognomonic laboratory ... (Clinical Dx). ... Arthritis, AS Treatment ... signs #symptoms #rheumatology
Guillain-Barre Syndrome - Summary Acute AIDP that presents with rapidly progressive flaccid weakness Epidemiology: • 1-2 cases/100,000 per
meningococcal, H1N1) Clinical ... nearly complete paralysis ... Guillain-Barre Clinical ... Treatment: • Plasmapheresis ... diagnosis #management #treatment
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