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management differential rheumatology hemophagocytic lymphohistiocytosis oncology syndrome vasculitis accaha acidosis behcet cardiology chf classes clinical congestive cutaneous dermatology dermpath disease
Hemophagocytic Lymphohistiocytosis (HLH) Pathophysiology: Triggering factor (infection,...)→Activation of CD8 T cells (IFN-y) → Excessive activation of macrophages
Autoimmune diseases: SLE ... Drugs, Unknown cause ... Treatment: • ... #management #treatment ... #summary #rheumatology
Dermatological semiology of Cutaneous Vasculitis Clinicopathologic correlations • Purpura, papules, pustules, necrosis: involvement of small vessels
Identification of causes ... in the context ... disease (10%) : SLE ... #semiology #signs ... #lesions #diagnosis
Leukostasis vs Tumor Lysis Syndrome Leukostasis: • Pathophysiology: Large, immature blasts and high WBC count cause hyperviscosity
high WBC count cause ... WBC >100k, + lab signs ... intracellular contents ... Syndrome #TLS #diagnosis ... #management #hematology
In order to better classify heart failure, the American College of Cardiology Foundation and the American
Below one can see ... With treatment, ... show symptoms or signs ... #Diagnosis #Cardiology ... #Stages #Classes
Post-Transplantation Lymphoproliferative Disorders (PTLD) Definition: Lymphoid and/or plasmacytic proliferations that occur as a result of immunosuppression in
Conditioning regimen Signs ... symptoms, unexplained hematologic ... EBV viral load, signs ... and classification ... to 50% of PTLD cases
Hodgkin's Lymphoma Overview Hodgkin's lymphoma (HL) is an uncommon hematological malignancy arising from mature B cells. It
) Classification ... lymph node biopsy (diagnostic ... Hodgkin Lymphoma Treatment ... #classification ... #hematology #oncology
Causes of Lactate Elevation, Lactic Acidosis - Differential Diagnosis The most common causes of hyperlactatemia are usually:
again we might see ... appropriate clinical context ... before beginning treatment ... Arterial Oxygen Content ... #typeb #classification
Behçet's Syndrome Systemic disease associated with inflammation of multiple organs, small-vessel vasculitis and large-vessel vasculopathy Epidemiology: • Young
common in Asia • HLA-B51 ... Oral aphthae : SLE ... • Arthritis: SLE ... Arthritis, AS Treatment ... #management #signs
Hemophagocytic Lymphohistiocytosis (HLH) High mortality without prompt recognition and management. HLH is a critical diagnostic consideration in
hyperinflammatory syndrome caused ... search for and treatment ... Presentation • Common Signs ... Treatment Approach ... #Management #Hematology
Vasculitis and Vasculitides - Differential Diagnosis Framework When to Consider Vasculitis: • Purpura, ischemic skin lesions •
tract, and often causes ... purpura: strong sign ... vasculitis, and SLE ... #rheumatology # ... classification
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