17 results
oncology chronic cll disease eosinophilia eosinophils hes leukemia activation algorithm anemia aplastic apml calcium capillary clarksons classification common cppd cvid
Hypereosinophilia and Hypereosinophilic Syndrome • Secondary Hypereosinophilic Syndrome • Clinically Relevant HES Variants • When to
Syndrome • Clinically ... disorders • Diagnosis ... and Treatment Algorithm ... #Hematology #eosinophilia ... #management #algorithm
Chronic Lymphocytic Leukemia (CLL) - Summary Overview: • Most common leukemia in adults • Disorder of
immunophenotype Clinical ... Complications: 1) Infection ... Leukemia #oncology #hematology ... #hemeonc #diagnosis ... #management
Hypereosinophilia Syndrome (HES) - Diagnosis and Management Definition: An absolute eosinophil count (AEC) greater than 1500 and
Hypereosinophilia ... than 1500 and clinical ... hypersensitivity - Infection ... Myeloproliferative HES - Lymphocytic ... #hematology #differential
Chronic Lymphocytic Leukemia - Summary Cancer affecting lymphocytes/Mature B cell neoplasm • Lymphocytes accumulate in large numbers
Orange or Hep C Clinical ... weeks without infection ... Lymphocytosis on CBC ... microglobulin Treatment ... workup #oncology #hematology
Common Variable Immunodeficiency (CVID) What? CVID: Immunodeficiency disorder with hypogammaglobulinemia -> increased infection risk secondary to impaired B-cell
to 8 years Clinical ... Granulomatous lymphocytic ... : • Nephrotic syndrome ... hypogammaglobulinemia #immunology #hematology ... #diagnosis #management
Differentiation Syndrome in APML Epidemiology: • Incidence: common in APL (2-48% depending on the study) • Triggers:
Differentiation Syndrome ... Triggers: ATRA treatment ... if high risk if WBC ... : Infection (sepsis ... #management #hematology
Aplastic Anemia - Overview Who? • M = F • 3 peaks: 1) Childhood 2) 15-25 years 3) >60 years What? • Aplastic anemia
Aplastic Anemia Clinical ... • ↓ WBC • ↓ ... aplastic anemia Treatment ... Anemia #oncology #hematology ... #diagnosis #management
Hemophagocytic Lymphohistiocytosis (HLH) Definition: Overwhelming clinical syndrome associated with excessive macrophage activation and cytokine storm due to
: Overwhelming clinical ... syndrome associated ... : • Infection ... #management #treatment ... #hematology
Sjogren's Syndrome Overview Epidemiology: • F > M: 9:1 • 5-6th Decades (can be any age) Autoimmune exocrinopathy multisystemic disease
salivary ducts Clinical ... phenomenon (16%) MSK ... Adenocarcinoma Treatment ... #Rheumatology # ... Diagnosis #Management
SAPHO Syndrome Summary What? SAPHO syndrome is a rare chronic inflammatory disorder of bone, joint, and skin characterized
: • A clinical ... causes such as infectious ... and lower jaw Treatment ... #Rheumatology # ... diagnosis #management
No results found for "WBC treatment diagnosis clinical msk infectiousdiseases pocus syndrome infections rheumatology management hematology hypereosinophilia lymphocytic"
Try removing search terms or sorting by relevance
Or Upload an image for you and others searching for #WBC #treatment #diagnosis #clinical #msk #infectiousdiseases #pocus #syndrome #infections #rheumatology #management #hematology #hypereosinophilia #lymphocytic