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hematology oncology hemeonc chronic hemolytic hemophagocytic hlh leukemia lymphocytic lymphohistiocytosis rheumatology treatment acquired activation aplastic ascorbicacid cap causes classification common
Diagnostic Framework for Hemolysis - Intravascular vs Extravascular Causes Intravascular Hemolysis: • Mechanical Trauma (Microangiopathic hemolytic anemia):
Diagnostic Framework ... hemolytic anemia ... : Thrombotic thrombocytopenic ... ) (e.g. lupus, CLL ... #hematology #anemia
Peripheral blood findings in microangiopathic hemolytic anemia. DIC is a clinical and laboratory diagnosis, not
hemolytic anemia ... DIC is a clinical ... and laboratory diagnosis ... non-specific red cell ... #Hematology #Pathology
Chronic Lymphocytic Leukemia (CLL) - Summary Overview: • Most common leukemia in adults • Disorder of
Lymphocytic Leukemia (CLL ... immunophenotype Clinical ... 5) Symptoms of anemia ... or thrombocytopenia ... #management
Chronic Lymphocytic Leukemia - Summary Cancer affecting lymphocytes/Mature B cell neoplasm • Lymphocytes accumulate in large numbers
Orange or Hep C Clinical ... Diagnosis: • ... • Neutropenia, anemia ... , thrombocytopenia ... Lymphocytic #Leukemia #diagnosis
Hemophagocytic Lymphohistiocytosis (HLH) Clinical Features: Fever, Splenomegaly, Hepatomegaly, Lymphadenopathy, Confusion Classic lab findings in HLH: ↑↑ ferritin, Anemia,
Lymphohistiocytosis (HLH) Clinical ... : ↑↑ ferritin, Anemia ... , Thrombocytopenia ... d-dimer, ↓ NK cell ... #hematology #criteria
Heparin Induced Thrombocytopenia (HIT) - Diagnosis and Management - GrepMed Handbook Presentation: • Plts ↓50% (nadir
Clinical Suspicion ... D/c all heparin ... non-heparin A/C if clinical ... #Diagnosis #Management ... #Treatment #Hematology
Aplastic Anemia - Overview Who? • M = F • 3 peaks: 1) Childhood 2) 15-25 years 3) >60 years What? • Aplastic anemia
Aplastic Anemia ... Clinical Presentation ... infections/fevers • Thrombocytopenia ... #oncology #hematology ... #diagnosis #management
Common Variable Immunodeficiency (CVID) What? CVID: Immunodeficiency disorder with hypogammaglobulinemia -> increased infection risk secondary to impaired B-cell
to impaired B-cell ... to 8 years Clinical ... specifically immune thrombocytopenia ... autoimmune hemolytic anemia ... #diagnosis #management
Scurvy (Vitamin C Deficiency) - Diagnosis and Management Vitamin C is required for hydroxylation of proline residues
Deficiency) - Diagnosis ... and Management ... poor nutrition Clinical ... cutaneous vasculitis, thrombocytopenia ... #Management
Macrophage Activation Syndrome (MAS) Classified among the secondary or acquired forms of haemophagocytic lymphohistiocytosis (sHLH) What? A subset of
Fever is the main clinical ... with leukopenia, anemia ... , and thrombocytopenia ... Activation #Syndrome #Diagnosis ... #Management #Hematology
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