16 results
management hemophagocytic hlh lymphohistiocytosis treatment disease radiology activation aliem anemia antiphospholipid apls behcet cancer capillary clarksons contusion cryofibrinogenemia ctchest deficiency
Hypereosinophilia and Hypereosinophilic Syndrome • Secondary Hypereosinophilic Syndrome • Clinically Relevant HES Variants • When to
• Clinically ... disorders • Diagnosis ... and Treatment Algorithm ... #HES #Hematology ... #management #algorithm
Iron Deficiency Anemia - Differential Diagnosis Algorithm Labs: Ferritin, iron, transferrin, TIBC, TSAT, sTfR • Blood loss:
: Ferritin, iron ... Gastrectomy, WHDA syndrome ... diet, Alcoholism, Tea-toast ... #Algorithm #ferritin ... #hematology
Macrophage Activation Syndrome (MAS) Classified among the secondary or acquired forms of haemophagocytic lymphohistiocytosis (sHLH) What? A subset of
Clinical Presentation ... Fever is the main clinical ... dehydrogenase • ↑ Ferritin ... #Diagnosis #Management ... #Hematology #Rheumatology
Susac Syndrome - Clinical Triad - Central nervous system dysfunction - Branch retinal artery occlusion -
Susac Syndrome - ... Clinical Triad ... disease flares - 2-year ... SusacSyndrome #Triad #Diagnosis ... #Management #Rheumatology
Hemophagocytic Lymphohistiocytosis (HLH) Definition: Overwhelming clinical syndrome associated with excessive macrophage activation and cytokine storm due to
: Overwhelming clinical ... syndrome associated ... Diagnosis via genetic ... cell activity • Ferritin ... management #treatment #hematology
Hemophagocytic Lymphohistiocytosis (HLH) Pathophysiology: Triggering factor (infection,...)→Activation of CD8 T cells (IFN-y) → Excessive activation of macrophages
accumulation of clinical ... Assessment • Clinical ... dysfunction, ↑ Ferritin ... Nicolas Taar ... treatment #summary #rheumatology
Cryofibrinogenemia Summary Cryofibrinogenemia Epidemiology: • 40-70 years with a modest female predominance Cryofibrinogenemia: • The precipitation of a
Cryofibrinogenemia Clinical ... : • + Clinical ... Antiphospholipid syndrome ... #rheumatology # ... hematology
Behçet's Syndrome Systemic disease associated with inflammation of multiple organs, small-vessel vasculitis and large-vessel vasculopathy Epidemiology: • Young
association • M > F Clinical ... (Clinical Dx). ... ) Differential Diagnosis ... Giant retinal tears ... signs #symptoms #rheumatology
Normal IUP Findings 1) Yolk sac: Round fluid-filled structure within the gestational sac, located in the
Small mass located near ... the yolk sac #Diagnosis ... #Clinical #EM # ... Obgyn #Radiology ... TransAbdmonial #POCUS
Sjogren's Syndrome Overview Epidemiology: • F > M: 9:1 • 5-6th Decades (can be any age) Autoimmune exocrinopathy multisystemic disease
Diagnosis: • Dry ... salivary ducts Clinical ... Nephrogenic DI Hematologic ... Symptomatic: artificial tears ... #Rheumatology #
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