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diagnosis blood differential disorders hemeonc hemophagocytic histiocytosis hlh hypertension igg4 langerhans lch lymphohistiocytosis lymphoproliferative oncology phtn post product ptld pulmonary
Clinical Classification of Pulmonary Hypertension 1. Pulmonary arterial hypertension from pulmonary vasculopathy Idiopathic pulmonary arterial hypertension Heritable gene mutations
Clinical Classification ... protein receptor type ... multifactorial mechanisms Hematologic ... pulmonary Langerhans cell ... #Differential #Causes
Post-Transplantation Lymphoproliferative Disorders (PTLD) Definition: Lymphoid and/or plasmacytic proliferations that occur as a result of immunosuppression in
hematopoietic cell ... symptoms, unexplained hematologic ... Diagnosis and classification ... to 50% of PTLD cases ... oncology #diagnosis #management
Blood Product Transfusions One Pager Summary Type and screen - determines blood type and detects in recipient
Pager Summary Type ... determines blood type ... potassium from lysed cells ... Transfusions #diagnosis #management ... #hematology #reactions
IGG-4 RELATED DISEASE WHAT? • A chronic, immune-mediated fibroinflammatory disease with tumefactive infiltration of IgG4+ plasma cells
- Organ dysfunction ... progressive organ dysfunction ... • Pancreas: Type ... complement • Classification ... #Rheumatology
Langerhans Cell Histiocytosis (LCH) Granulomatous Lesions comprising langerin-positive histiocytes and an inflammatory infiltrate can arise in virtually
, a type of dendritic ... various tissues, leading ... • Endocrine Dysfunction ... marrow: Organ dysfunction ... Histiocytosis #Diagnosis #Management
Hemophagocytic Lymphohistiocytosis (HLH) High mortality without prompt recognition and management. HLH is a critical diagnostic consideration in
cytopenias and organ dysfunction ... hyperinflammatory syndrome caused ... Persistent fever, organ dysfunction ... Types of HLH • ... #Hematology #HemeOnc
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