19 results
Heparin Induced Thrombocytopenia (HIT) - Likelihood, Diagnosis and Management
 - HIT Suspected
 - Calculate 4T Score
- Likelihood, Diagnosis ... and Management ... - HIT Suspected ... Thrombocytopenia #Algorithm #Diagnosis ... #Management #Hematology
Our approach to the diagnosis and initial management of patients with suspected HIT. Our approach is
approach to the diagnosis ... and initial management ... patients in whom diagnostic ... #Diagnosis #Management ... #Hematology #HIT
Aplastic Anemia - Illness Script
Signs and symptoms:
 • Recurrent infections from neutropenia
 • Mucosal bleeding from
Symptomatic anemia Diagnosis ... cyclosporine A, ATG ... Aplastic #Anemia #diagnosis ... #management #treatment ... #hematology
Heparin Induced Thrombocytopenia (HIT) - Diagnosis and Management - GrepMed Handbook

Presentation: 
 • Plts ↓50% (nadir
) - Diagnosis and ... Management - GrepMed ... obtain Anti-PF4 Ab ... after Dx if PF4-Ab ... #Hematology #HemeOnc
Adult-Onset Still's Disease
Clinical triad: Fever, Arthralgia/arthritis, Skin rash ± odynophagia
+ Biological inflammation: Increased neutrophils, Hyperferritinemia, decreased
arthritis, Skin rash ... Differential Diaqnoses ... Coxsackie, CMV, EBV, HIV ... #management #treatment ... #rheumatology
Kawasaki Disease (KD) - Diagnosis and Management Summary

Kawasaki Disease (KD) is the most common vasculitis of
and Management ... Conjunctivitis, Mucositis, Rash ... , diarrhea • It ... Polymorphous rash ... KD #vasculitis #rheumatology
Macrophage Activation Syndrome (MAS)
Classified among the secondary or acquired forms of haemophagocytic lymphohistiocytosis (sHLH)

What?
A subset of
Petechial or purpuric rash ... Activation #Syndrome #Diagnosis ... #Management #Hematology ... #Rheumatology
Common Variable Immunodeficiency (CVID)

What?
CVID: Immunodeficiency disorder with hypogammaglobulinemia -> increased infection risk secondary to impaired B-cell
50,000 patients • Avg ... and M panel Management ... Epstein-Barr syndrome, HIV ... hypogammaglobulinemia #immunology #hematology ... #diagnosis #management
Hemophagocytic Lymphohistiocytosis (HLH)
Definition: Overwhelming clinical syndrome associated with excessive macrophage activation and cytokine storm due to
It is rare in presentation ... It presents as an ... Diagnosis via genetic ... #management #treatment ... #hematology
Disseminated Intravascular Coagulation (DIC) Overview

Increased Clotting and Consumption of Clotting Factors

Findings:
 • Bleeding
 • Recent history
promyelocytic leukemia) or ABO ... deficiency) • HIT ... #Coagulation #diagnosis ... causes #treatment #management ... #hematology