5 results
diagnosis activation behcet cppd macrophage polychondritis pseudogout pyrophosphate relapsing signs tafro thrombocytopenia
Macrophage Activation Syndrome (MAS) Classified among the secondary or acquired forms of haemophagocytic lymphohistiocytosis (sHLH) What? A subset of
(HLH) that develops ... erythematosus [SLE ... Treatment: • Corticosteroids ... #Diagnosis #Management ... #Hematology #Rheumatology
Behçet's Syndrome Systemic disease associated with inflammation of multiple organs, small-vessel vasculitis and large-vessel vasculopathy Epidemiology: • Young
Behçet's Syndrome ... Oral aphthae : SLE ... Treatment: • Oral ... #management #signs ... #symptoms #rheumatology
Pseudogout Summary - Calcium Pyrophosphate Deposition Disease (CPPD) Pathophysiology: Pyrophosphate produced by chondrocytes likely precipitates with calcium to
Pathophysiology ... a linear opacity ... Crowned Dens Syndrome ... #Disease #Rheumatology ... #diagnosis #management
Relapsing Polychondritis What is it? Recurrent inflammation of the cartilage in the body (Autoimmune disorder) Who? • Most frequently: 40
chondritis • Ocular ... : • SLE • RA - ... Sarcoidosis • Behcet ... Polychondritis #rheumatology ... #diagnosis #management
TAFRO TAFRO syndrome was first described in 2010, standing for: - Thrombocytopenia - Anasarca - Fever - Reticulin fibrosis - Organomegaly TAFRO syndrome
including systemic lupus ... erythematosus (SLE ... and the systemic symptoms ... Hypoalbuminemia Treatment ... #rheumatology #
No results found for "Lineage ocular syndrome pathophysiology hematology behcets management treatment rheumatology lymphohistiocytosis disease lupus deposition hlh sle calcium symptoms mas"
Try removing search terms or sorting by relevance
Or Upload an image for you and others searching for #Lineage #ocular #syndrome #pathophysiology #hematology #behcets #management #treatment #rheumatology #lymphohistiocytosis #disease #lupus #deposition #hlh #sle #calcium #symptoms #mas