48 results
diagnosis management differential rheumatology syndrome nephrology hepatology algorithm causes chronic oncology signs symptoms activetb adultonset aids barre cancer cirrhosis classification
Gastritis and Peptic Ulcer Disease - Etiology, Diagnostics, Treatment and Complications #Diagnosis #Pathophysiology #Management #Gastritis #PepticUlcerDisease #PUD
and Peptic Ulcer Disease ... , Diagnostics, Treatment ... and Complications ... #Diagnosis #Pathophysiology
Bell's Palsy Bell’s Palsy is a damage, acute weakness, or paralysis of the Facial nerve (7th CN),
Herpes simplex virus ... - Epstein-Barr virus ... Burgdorferi (Lymes disease ... #Bells #Palsy #neurology ... #anatomy #pathophysiology
Sickle Cell Disease - Pathophysiology of disease and complications Due to the deformed shape, HbS induces
- Pathophysiology ... complications ... #Pathophysiology ... #Complications ... #Hematology #Sequelae
Adult-Onset Still's Disease Clinical triad: Fever, Arthralgia/arthritis, Skin rash ± odynophagia + Biological inflammation: Increased neutrophils, Hyperferritinemia, decreased
Adult-Onset Still's Disease ... autoinflammatory diseases ... , Schnitzler) Complications ... diagnosis #management #treatment ... #rheumatology
CNS Manifestations of Systemic Lupus Erythematosus (SLE) Clinical Manifestations: Demyelinating Syndrome, Headache, Movement disorders, Seizure disorders, Aseptic
Cerebrovascular Disease ... , PRES Pathophysiology ... Puncture, EEG Treatment ... Erythematosus #SLE #CNS #neurology ... #rheumatology #
Treatment of Non-hepatitis C virus Cryoglobulinemia Vasculitis - French Vasculitis Study Group MONOCLONAL CRYOGLOBULINEMIA (TYPE 1) IgM
Treatment of Non-hepatitis ... C virus Cryoglobulinemia ... /or refractory disease ... Vasculitis #Management #Rheumatology
Polycythemia Vera (PV) - Diagnosis and Management Summary Diagnostic Criteria: • Elevated hemoglobin and/or hematocrit AND •
symptoms, signs, and complications ... Splenomegaly Treatment ... • Treatment is ... von Willebrand disease ... #hematology
Adult-Onset Still's Disease (AOSD) Rare inflammatory disorder of unknown etiology, difficult to diagnose because of heterogenous presentation.
Adult-Onset Still's Disease ... Life-threatening complications ... synovitis (40%) Treatment ... AdultOnset #Stills #Disease ... #AOSD #rheumatology
Hemophagocytic Lymphohistiocytosis (HLH) Pathophysiology: Triggering factor (infection,...)→Activation of CD8 T cells (IFN-y) → Excessive activation of macrophages
Lymphohistiocytosis (HLH) Pathophysiology ... Infections+++: Virus ... • Autoimmune diseases ... Adult-onset Still disease ... Unknown cause Treatment
Causes of Fatigue - Differential Diagnosis Algorithm Endocrine • Hypo/Hyperthyroidism • Diabetes • Pituitary Insufficiency • Adrenal
Neoplastic / Hematologic ... Epstein-Barr Virus ... Obstructive Pulmonary Disease ... Neurologic •
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