32 results
diagnosis hematology differential disease oncology eosinophilia hemeonc hemophagocytic heparin hit hlh induced infections lymphohistiocytosis pharmacology signs symptoms syphilis thrombocytopenia activation
Hypereosinophilia and Hypereosinophilic Syndrome • Secondary Hypereosinophilic Syndrome • Clinically Relevant HES Variants • When to
• Clinically ... Diagnosis and Treatment ... #HES #Hematology ... eosinophils #diagnosis #management ... #algorithm
Behcet's Syndrome - Treatment Ulcers: • Treatment: Topical steroids • Prevention: Colchicine • Azathioprine for refractory disease Arthritis:
Behcet's Syndrome ... refractory disease Skin ... refractory lesions Ocular ... #Treatment #management ... #pharmacology #rheumatology
2019 EULAR recommendations for thrombosis in (Antiphospholipid Syndrome) APS Venous Thrombosis - Arterial Thrombosis INR Target Duration Recurrence Dr. Laurent ARNAUD
2019 EULAR recommendations ... Antiphospholipid Syndrome ... Antiphospholipid #Syndrome ... #APS #management ... #hematology #treatment
Sarcoidosis - Skin Manifestations This is a quick overview of some of the cutaneous manifestations of sarcoidosis.
Sarcoidosis - Skin ... Lupus Pernio • Macular ... Sarcoidosis #diagnosis #clinical ... #differential #treatment ... #photo #dermatology
Eosinophil Disorders Testing Algorithm INDICATIONS FOR TESTING: • Peripheral blood eosinophilia/hypereosinophilia uncovered incidentally during medical evaluation or
Disorders Testing Algorithm ... glucocorticoid treatment ... organ-specific signs ... symptoms (eg, skin ... Differential #diagnosis #hematology
Behçet's Syndrome Systemic disease associated with inflammation of multiple organs, small-vessel vasculitis and large-vessel vasculopathy Epidemiology: • Young
(Clinical Dx). ... Arthritis, AS Treatment ... #diagnosis #management ... #signs #symptoms ... #rheumatology #
SAPHO Syndrome Summary What? SAPHO syndrome is a rare chronic inflammatory disorder of bone, joint, and skin characterized
Rheumatic pain Clinical ... and lower jaw Treatment ... #Rheumatology # ... diagnosis #management ... #Dermatology
Adult-Onset Still's Disease Clinical triad: Fever, Arthralgia/arthritis, Skin rash ± odynophagia + Biological inflammation: Increased neutrophils, Hyperferritinemia, decreased
Still's Disease Clinical ... Arthralgia/arthritis, Skin ... • Ocular: uveitis ... Disease #diagnosis #management ... #treatment #rheumatology
Polycythemia Vera (PV) - Diagnosis and Management Summary Diagnostic Criteria: • Elevated hemoglobin and/or hematocrit AND •
Diagnosis and Management ... present, symptoms, signs ... • Treatment algorithms ... PV #Diagnosis #Management ... #hematology
Our approach to the diagnosis and initial management of patients with suspected HIT. Our approach is
diagnosis and initial management ... based primarily on clinical ... and to adjust treatment ... #Hematology #HIT ... Thrombocytopenia #Algorithm
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