27 results
Causes of Splenomegaly - Differential Diagnosis Algorithm
Infectious
 • Bacterial
 • Viral (EBV)
 • Parasitic
 • Fungal
Congestive
- Differential Diagnosis ... Non-Malignant • Amyloidosis ... Myeloproliferative disorders ... myelofibrosis) Inflammatory ... Algorithm #Causes #Hematology
Acquired von Willebrand Syndrome - Diagnosis and Management
 • Autoantibodies to vWF: Lymphoproliferative disorders (e.g. lymphoma,
von Willebrand Syndrome ... - Diagnosis and ... Management • ... thrombocythemia), Autoimmune disease ... #Diagnosis #Management
Purpura - Differential Diagnosis Framework

Non-blanchable, dark red to purple, hemorrhagic skin lesions that result from leakage
- Differential Diagnosis ... Kasabach-Merritt syndrome ... Dermal Vessels: - Amyloidosis ... Gardner-Diamond syndrome ... #hematology #rheumatology
Amyloidosis - Summary
Group of disorders associated with extracellular deposition of fibrils formed from low-molecular-weight proteins in
Group of disorders ... (AA) → Chronic Inflammatory ... the extent of disease ... : • Nephrotic syndrome ... Carpal tunnel syndrome
CNS Manifestations of Systemic Lupus Erythematosus (SLE)

Clinical Manifestations: Demyelinating Syndrome, Headache, Movement disorders, Seizure disorders, Aseptic
Demyelinating Syndrome ... Cerebrovascular Disease ... Treatment: • Inflammatory ... CNS #neurology #rheumatology ... #management #treatment
Antinuclear Antibodies (ANA)
ANA or Anti-NucIear Antibody refers to antibodies against antigens in the nucleus → like
SLE), Sjogren's Syndrome ... Lymphoproliferative Disorders ... Drug-Induced, Inflammatory ... ANA #patterns #rheumatology ... #diagnosis #differential
Macrophage Activation Syndrome (MAS)
Classified among the secondary or acquired forms of haemophagocytic lymphohistiocytosis (sHLH)

What?
A subset of
background of a highly inflammatory ... disease How? ... release of pro-inflammatory ... #Diagnosis #Management ... #Hematology #Rheumatology
Cardiomyopathies 

Manifestations of cardiomyopathy (CM) range from microscopic alterations in cardiac myocytes to fulminant Heart Failure
systemic (multiorgan) disorders ... Infiltrative (Amyloidosis ... Hemochromatosis, Fabry's disease ... ) • Inflammatory ... Cardiomyopathies #cardiology #diagnosis
Bleeding and Bruising - Disorders of Hemostasis - Differential Diagnosis Framework

== Quantitative or Qualitative defect in
- Differential Diagnosis ... von Willebrand syndrome ... Vasculitis • Amyloidosis ... #Differential #Diagnosis ... #Hematology
Adult-Onset Still's Disease (AOSD)
Rare inflammatory disorder of unknown etiology, difficult to diagnose because of heterogenous presentation.
Adult-Onset Still's Disease ... (AOSD) Rare inflammatory ... disorder of unknown ... #AOSD #rheumatology ... #diagnosis #management