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leukemia
Question | Answer |
---|---|
What is leukemia | A cancer that originates in the bone marrow from a single cell and multiples affecting healthy blood cells |
How does acute and chronic differ? | Acute are undifferentiated immature blast cells and have a short survival time and chronic mature nonfunctional cells with longer survival rate |
What is the difference between myeloid and lymphoid cells? | Myeliod turn into functional RBCs, PLTs, WBCs and lymphoids make t-cells or b-cells |
What genetic factors are associated w leukemia? | trisomy 21 (downs) and kliefelter's syndrome (XXY) |
What other factors are associated w leukemia? | virus (Epstein Bar, HIV), radiation, Drugs (chemo), chemicals (solvents, benzenes) |
What labs are associated w leukemia? | anemia (>4.5), neutropenia (>1,700), thromobocytopenia (>150,000), hyperuricemia (<6.8), increased LDH (<115) |
How is a cytogenic analysis taken? | through bone marrow |
What are S/S of neutropenia? | fever, abd pain, resp infection, perrectal abscess, mucositis, adenopathy |
What are S/S of thrombocytopenia? | petchiae, purpura, bleeding, gums, epitaxis, retinal hemorrhage, intracranial bleed |
What are S/S of anemia? | Pallor, dyspnea, fatigue, maliaise |
What are S/S of leukemia infiltrates? | HA, splenomeagaly, hepatomeagaly, pain and swelling in joints, lyphadenopathy |
What are the primary goals of treatment? | hematopoesis, eliminate residula dz, treat extramedullary sites, suppress resistant clones |
What are the options for systemic treatment? | chemo, target, and immunotherpay |
How does acute treatment start and end? | Starts with remission induction chemo and ends with post-remission consolidation |
What leukemia uses CNS prophylaxis via intrathecal? | ALL |
Which leukemia uses stem cell transplant? | AML, CLL |
Which leukemmia does a watchful waiting? | CLL |
Which leukemia uses target therapy indefinitely? | CML |
Which leukemia has auer rods? | AML |
What factors make a PT more at risk for a poor prognosis? | previous chemo or radiation, <70, WBC<100,000, previous blood disorder, infection, M5, or poor cytogenetics |
What is the goal for AML? | Bone marrow supression |
When is a bone marrow aspiration done? | day 14 |
What determines if "remission?" | <5% |
When is a bone marrow aspiration repeated? | 3-4 weeks post induction |
What is used during relapse of AML? | Gemtuzumab ozogamicin (Mylotarg) |
What is distinct of Leukemia M3? | contains promyelocytes, 40% in DIC |
What made Leukemia M3 have a much better prognosis? | all-transretinoic acid (ATRA) |
How many consolidation cycles does APL have to go through? | 2 |
What are the three stages for CML? | chronic, accelerated and blast crisis |
What are the S/S of chronic phase? | pallor, night sweats, fatigue, dyspnea, anemia, anorexia, wt loss, sternal tenderness, fullness, abd distension |
What are the S/S of accelerated phase? | chronic S/S + fever, hepatomeagaly, hypermetabolism, splenomegaly, lymphadenopathy |
What is the survival rate expectancy of accelerated phase? | one year |
What are the nursing priorities for a neutropenic pt? | watch for fever, ATB, ATF, cultures, CXR |
what nincreases the risk of leukocytosis? | WBCs <50,000 |
What are the consequences of hyperurecimia? | gout like symptoms, renal obstruction, kidney failure |
What are the treatments for hyperuricemia? | allopurinol, hydration, and alkalization of urine |
Where to most lymphomas arise from? | b-cells |
What type of cells do Hodgkins lymphoma have? | Reed-sternberg cells |
What grade is Burkitts? | high grade, agressive |
Which is more common? NHL or HL? | NHL |
What are the risk factors of HL? | Epstein Bar, HIV, Mono, same sex siblings |
What are the risk factors for NHL? | hair dying, asbestos, rubber production, radiation, EBV, H.pylori |
Where do lymphadenopathies occur in HL? | cervical, subclavicular, and medistinal |
Where to lymphadenopathies occur in NHL? | Extranodule |
Watchful waiting is associated with which, NHL? or HL? | NHL |