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52 Cards in this Set

  • Front
  • Back
what conditions is eosinophilia seen in?
type I hypersensitivity, invasive helminthic infection, polyarteritis nodosa, addison's disease (cortisol deficiency)
when is basophilia seen?
chronic myeloproliferative disorders
atypical lymphocytosis?
due to infection or drugs, antigenically stimulated lymphocytes have prominent nucleoli and abundant blue cytoplasm
antibody detected early/late in infectious mono?
early: antiviral capsid antigen (VCA) antibodies;
late: anti-epstein barr nuclear antigen (EBNA) antibodies
most sensitive cell to destruction by radiation?
lymphocytes
when see lymphopenia?
HIV, immunnodeficiency, immune destruction (SLE), corticosteroids, radiation
when see monocytosis?
chronic infection, autoimmune disease, malignancy
gender epidemiology of leukemias?
male > female
leukemia risk factors?
chromosomal abnormalities, ionizing radiation, chemicals, alkylating agents, chronic myeloproliferative diseases, paroxysmal nocturnal hemoglobinuria, cigarette smoking, immunodeficiency diseases
most common leukemia in children (newborn - 14 yo)?
acute lymphoblastic leukemia (ALL)
most common leukemia in 15-39 yo?
acute myeloblastic leukemia (AML)
most common leukemias in 40-60 yo?
acute myeloblastic leukemia (AML) and chronic myelogenous leukemia (CML)
most common leukemia in >60 yo?
chronic lymphocytic leukemia (CLL)
clinical findings in acute leukemia?
fever, bleeding, fatigue, bone pain
common organs of mets in ALL?
CNS, testicles
lab findings in acute leukemia?
blasts in peripheral blood, normocytic to macrocytic anemia, thrombocytopenia, hypercellular bone marrow with >20% blasts
lab findings in chronic leukemia?
some evidence of maturation of cells, normocytic to macrocytic anemia, thrombocytopenia, hypercellular bone marrow with <10% blasts
which chronic leukemia is exception to clinical finding of thrombocytopenia?
CML, thrombocytosis occurs in 40% of cases
chronic myeloproliferative disorders?
polycythemia vera, chronic myelogenous leukemia, myeloid metaplasia with myelofibrosis, essential thrombocythemia
absolute polycythemia?
increase in bone marrow production of rbcs resulting in increased rbc count and rbc mass
appropriate absolute polycythemia?
hypoxic stimulus for EPO
mutation in polycythemia vera?
JAK2 gene on short arm of chromosome 9 (same mutation may manifest as myelofibrosis and myeloid metapolasia or essential thrombocythemia)
clinical findings in polycythemia vera?
hepatosplenomegaly, ruddy face, thrombotic event, impaired CNS circulation, pruritis after bathing, peptic ulcer disease, gout
best initial lab test for polycythemia vera?
decreased EPO
risk factors for CML?
ionizing radiation and benzene
mutation in CML?
philadelphia chromosome (t9;22 translocation): BCR-ABL fusion gene
basophilia is prominent in which leukemia?
CML
CML prognosis?
~90% 5 year survival
pathogenesis of myelofibrosis and myeloid metaplasia?
ineffective erythropoiesis, dysplastic megakaryocytes, immature granulocytes, reactive myelofibrosis; marrow fibrosis occurs earlier than in other chronic myeloproliferative diseases
clinical findings in myelofibrosis and myeloid metaplasia?
massive splenomegaly with portal HTN; splenic infarcts with left-sided pleural effusions
treatment for myeloproliferative diseases?
hydroxyurea
lab findings in myelodysplastic syndromes?
severe pancytopenia, ringed sideroblasts, myeloblasts <20%
myelodysplastic syndromes may progress to which leukemia?
AML (acute myeloblastic leukemia)
clinical findings in AML?
DIC, gum infiltration
characteristic histological finding in AML?
auer rods: fused azurophilic granules in cytosol (NOT in CML)
mutation in acute promyelocytic leukemia?
t(15;17) translocation
subtypes of ALL?
early pre-B cell, pre-B cell, B cell, and T cell
mutation associated with favorable prognosis in early pre-B cell ALL?
t(12;21) translocation
clinical presentation of T cell ALL?
anterior mediastinal mass or acute leukemia
markers in B cell vs T cell ALL?
B is CD10(+), T is CD10(-), both are TdT(+) [terminal deoxynucleotidyl transferase]
lab findings in ALL?
>20% lymphoblasts in peripheral blood, normocytic anemia with thrombocytopenia
adult T cell leukemia association?
human T cell leukemia virus (HTLV-1)
pathogenesis of adult T cell leukemia?
activation of TAX gene, which inhibits the tp53 suppressor gene
bone lesions associated with adult T cell leukemia?
lytic: due to lymphoblast release of osteoclast-activating factor, associated with hypercalcemia
lab findings in adult T cell leukemia?
>20% lymphoblasts in peripheral blood, CD4(+), TdT(-)
most common overall leukemia?
CLL
which leukemia has increased incidence of immune hemolytic anemia?
CLL
lab findings in CLL?
lymphoblasts <10%, 'smudge' cells
precursor cell in CLL?
virgin B cells
only leukemia without lymphadenopathy?
hairy cell leukemia (HCL)
clinical findings in HCL?
splenomegaly, absence of lymphadenopathy, hepatomegaly, autoimmune vasculitis and arthritis
lab findings in HCL?
pancytopenia, leukemic cells with hair-like projections, increased reticulin fibers in bone marrow, (+)TRAP stain