19 results
hematology treatment rheumatology appendicitis differential disease eosinophilia eosinophils hemophagocytic hes hlh hypereosinophilia lymphohistiocytosis ultrasound acromegaly activation adominal algorithm anemia aplastic
POCUS diagnosis of acute appendicitis: (1) Blind-ended (2) Target shaped tubular structure (3) Originating from the cecum (4) Non-compressible (5) Non-peristalsing
POCUS diagnosis ... #Appendicitis #Abdominal ... #Appendix #Clinical ... #POCUS
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 Hypereosinophilia and Hypereosinophilic Syndrome • Secondary Hypereosinophilic Syndrome • Clinically Relevant HES Variants • When to
• Clinically ... disorders • Diagnosis ... #HES #Hematology ... #eosinophils #diagnosis ... #management #algorithm
Campylobacter Clinical • Fever • Abdominal pain • Diarrhea (bloody stools) • Vomiting
Campylobacter Clinical ... • Fever • Abdominal ... Guillain-Barré syndrome ... Management ... Campylobacter #Diagnosis
Appendicitis on POCUS What is your diagnosis? Resolution: appendicitis (criteria >6mm, noncompressible, blind-ended, no peristalsis). When diagnosed by
Appendicitis on POCUS ... When diagnosed by ... #Appendicitis #appendix ... #POCUS #clinical ... #ultrasound #abdominal
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 Renal Cell Carcinoma (RCC) - Diagnosis and Management Summary Clinical features - Classic triad (flank pain, hematuria,
Carcinoma (RCC) - Diagnosis ... and Management ... Summary Clinical ... and a palpable abdominal ... Budd Chiari syndrome
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 ... • Nonsurgical abdominal ... #diagnosis #management
Rhabdomyolysis - Differential Diagnosis Framework and Management Summary Causes of Rhabdomyolysis: • Trauma: - Immobilization - Crush injury - Compartment
- Differential Diagnosis ... Framework and Management ... Dermatomyositis Clinical ... Tachycardia - N/V - Abdominal ... #Management #causes
Common Variable Immunodeficiency (CVID) What? CVID: Immunodeficiency disorder with hypogammaglobulinemia -> increased infection risk secondary to impaired B-cell
to 8 years Clinical ... and M panel Management ... : • Nephrotic syndrome ... (Epstein-Barr syndrome ... #diagnosis #management
Macrophage Activation Syndrome (MAS) Classified among the secondary or acquired forms of haemophagocytic lymphohistiocytosis (sHLH) What? A subset of
Macrophage Activation Syndrome ... Clinical Presentation ... Fever is the main clinical ... #Diagnosis #Management ... #Hematology #Rheumatology
Aplastic Anemia - Overview Who? • M = F • 3 peaks: 1) Childhood 2) 15-25 years 3) >60 years What? • Aplastic anemia
Constitutional Syndromes ... Aplastic Anemia Clinical ... Constitutional Syndromes ... Anemia #oncology #hematology ... #diagnosis #management
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