18 results
Pivot-Shift Test in ACL-deficient Knee

This patient has pathologic varus alignment across the knee and a chronic
HTO) to correct his ... #ACL #Knee #Injury ... #ACLTear #clinical ... #PhysicalExam #Sports ... #Ortho #msk
Lachman test in ACL-deficient Knee

This patient has pathologic varus alignment across the knee and a chronic
HTO) to correct his ... #ACL #Knee #Injury ... #ACLTear #clinical ... #PhysicalExam #Sports ... #Ortho #anterior
Heparin Induced Thrombocytopenia (HIT) - Diagnosis and Management - GrepMed Handbook

Presentation: 
 • Plts ↓50% (nadir
(HIT) - Diagnosis ... Clinical Suspicion ... approach for post-test ... : Confirmatory test ... #Diagnosis #Management
Our approach to the diagnosis and initial management of patients with suspected HIT. Our approach is
and initial management ... laboratory tests ... #Diagnosis #Management ... #Hematology #HIT ... Heparin #Induced #Thrombocytopenia
Mallet Finger
Absence of a fracture does NOT exclude Mallet finger, the extension function of the DIP
joint needs to be clinically ... : Hyperflexion injury ... joint • Ortho ... Radiology #XRay #Diagnosis ... #Management #Hand
Disseminated Intravascular Coagulation (DIC) Overview

Increased Clotting and Consumption of Clotting Factors

Findings:
 • Bleeding
 • Recent history
organ damage Clinical ... deficiency) • HIT ... #Coagulation #diagnosis ... causes #treatment #management ... #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 ... to local skin injury ... Behcet syndrome (Clinical ... #management #signs ... #symptoms #rheumatology
Aplastic Anemia - Overview

Who?
• M = F
• 3 peaks:	1) Childhood	2) 15-25 years	3) >60 years

What?
• Aplastic anemia
Marrow (Toxic injury ... Aplastic Anemia Clinical ... infections/fevers • Thrombocytopenia ... Anemia #oncology #hematology ... #diagnosis #management
Macrophage Activation Syndrome (MAS)
Classified among the secondary or acquired forms of haemophagocytic lymphohistiocytosis (sHLH)

What?
A subset of
leukopenia, anemia, and thrombocytopenia ... Liver function tests ... Activation #Syndrome #Diagnosis ... #Management #Hematology ... #Rheumatology
Common Variable Immunodeficiency (CVID)

What?
CVID: Immunodeficiency disorder with hypogammaglobulinemia -> increased infection risk secondary to impaired B-cell
to 8 years Clinical ... specifically immune thrombocytopenia ... and M panel Management ... Epstein-Barr syndrome, HIV ... #diagnosis #management