140 results
diagnosis treatment hematology syndrome signs differential oncology pathophysiology algorithm summary dermatology infectiousdiseases lupus nephrology workup comparison hepatology infections sle anemia
Bell's Palsy Bell’s Palsy is a damage, acute weakness, or paralysis of the Facial nerve (7th CN),
Bell's Palsy Bell ... Bell’s palsy happens ... unknown but its clinically ... Burgdorferi (Lymes disease ... #Palsy #neurology
Sarcoidosis Non-caseating granulomas (Composed of T-helper & inflammatory cells) Clinical: • Disease fatal in 10% of
) Clinical: ... • Disease fatal ... exertion • Neurologic ... : Bell's palsy, ... Sarcoidosis #Diagnosis #Symptoms
Clinical Disease Characteristics and Suggested Algorithm for Diagnostic Evaluation of Patients With Symptoms of Polymyalgia Rheumatica #Diagnosis
Clinical Disease ... Patients With Symptoms ... #Diagnosis #Rheumatology
Von Willebrand Disease - Clinical Presentation, Diagnosis and Management - Dr. Eric Strong @DrEricStrong - Strong Medicine
Von Willebrand Disease ... - Clinical Presentation ... Diagnosis and Management ... VonWillebrand #Disease ... #hematology #treatment
Hodgkin's Lymphoma vs Non-Hodgkin's Lymphoma - Comparison Hodgkin's Lymphoma: • Epidemiology: young adults 20-30, older 50-70 •
• Clinical features ... - B symptoms ... Noncontiguous spread • Clinical ... Diagnosis of B-Symptoms ... #differential #hematology
Dysmorphic Red Blood Cells on Electron Microscopy This eyeSCANdy image shows dysmorphic red blood cells from the
Dysmorphic Red Blood Cells ... dysmorphic red blood cells ... ElectronMicroscopy #SEM #clinical ... #pathology #hematology ... #nephrology #Red
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 Adult-Onset Still's Disease Clinical triad: Fever, Arthralgia/arthritis, Skin rash ± odynophagia + Biological inflammation: Increased neutrophils, Hyperferritinemia, decreased
Adult-Onset Still's Disease ... Clinical triad ... autoinflammatory diseases ... #diagnosis #management ... #treatment #rheumatology
Cold Urticaria Prevalence - 0.05% in the population Disease onset - Mostly 2nd to 4th decades of life Causes
the population Disease ... life Causes and clinical ... and duration of symptoms ... angioedema Other symptoms ... Urticaria #diagnosis #rheumatology
Peripheral Blood Smear Analysis Hypochromia Megaloblastic Anemia Schistocytes: Microangiopathic hemolytic anemia (e.g. DIC, TTP, HUS) Microspherocytes: Autoimmune hemolytic anemia Sickled red
anemia Sickled red cells ... : Sickle cell disease ... Bite cells: G6PD ... Smear #Analysis #hematology ... interpretation #clinical
Behçet's Syndrome Systemic disease associated with inflammation of multiple organs, small-vessel vasculitis and large-vessel vasculopathy Epidemiology: • Young
association • M > F Clinical ... skin injury) • Neurologic ... Syndrome #diagnosis #management ... #signs #symptoms ... #rheumatology #
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