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41 Cards in this Set
- Front
- Back
What is the first line defense? |
T cells, cellular immunity |
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What are T-lymphocytes cells? |
from thymus, marrow; kill foreign cells or secrete substances to increase activity of phagocytes, responsible for delayed allergic reactions, transplant rejection and destruction of tumor cells *cellular immunity |
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What are b-lymphocytes cells? |
produced in bone marrow -differentiate into plasma cells which produce immunoglobulin (protein that destroys foreign matter) *Humoral immunity = antibodies |
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Role of neutrophil? |
-released into circulation within 6 hr -phagocytosis -first defense against bacterial infection |
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Role of monocytes? |
-convert to macrophages in the tissue -phagocytosis -second line of defense -pac man |
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Role of eosinophils? |
-phagocytosis of parasites -increase in allergic reactions -neutralize histamine |
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Role of basophils? |
Produce and store histamine (histamine provokes allergic reaction) -manifestations of inflammation |
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What is leukemia? |
-"white blood" -ratio of RBCs to WBCs is reversed -happens in childhood and adults |
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What is the pathophysiology of leukemia? |
-Proliferation of one type of WBC -malignant transformation of one stem cell (bad cell takes over and kills other good cells) -Major feature: crowds out other cells, which results in anemia/thrombocytopenia -WBCs are immature, do not function, high risk for infection |
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Common S&S of leukemia? |
*Fatigue (common) -LOA, wt loss, fever, infections -swelling -enlargement of spleen/liver -night sweats, easy bleeding bruising, purplish patches -pain/tenderness of joints/bones -SOB -Weakness |
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What is the survival rate? |
w/ out tx= dead 46% 5 year |
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What is acute myeloid? |
uncontrolled proliferation of myeloblasts (granulocytes) |
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How does AML develop? |
-DNA change of bone marrow and multiplies, huge explosion of unhealthy cells (leukemic blasts) = don't function normally and flushes all good out |
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What are some causes and risk factors with AML? |
Benzene down's syndrome radiation/chemo -cannot catch |
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What are S&S of AML? |
-Fatigue -SOB -pale skin -bruises with no cause -swollen gums -frequent minor infections (peri anal sores) |
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Tx of AML? |
Chemotherapy anti-tumor antibiotics -antimetabolics -DNA repair enzyme inhibitor ect. -stem cell transplant |
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What is chronic myeloid leukemia? |
unregulated growth of myeloid cells typically has 3 phases -chronic (may/may not have S&S) -Accelerated phase (Showing classic S&S, increase blasts cells, swollen spleen) -Blast crisis phase (lots of blasts, treated very aggressively) |
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What is the incidence of CML? Risk factors? |
-effects mainly adults >65 -5000 diagnosed/yr -RF: increased doses of radiation and other chemo -RF: Philedelphia chromosome: stuff that should be on chromosome 22 are on 9 |
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CML treatment? |
TX phase: return blood levels back to normal Chronic phase -imatinib mesylate -dasatinib -nilotinib Accelerated/blast crisis -interferon -busulfan -cytabine -hydroxyurea STEM cell transplant |
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What is acute lymphoctyic leukemia? |
characterized by excess lymphoblasts -most common type of cancer age 1-7 -most common leukemia for kids infancy- 19 |
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Risk factors for ALL? |
Unknown maybe X-rays or certain medications |
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ALL subtypes? |
BCell ALL T Cell ALL Humoral or cellular can be affected |
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ALL tx? |
stem cell transplant intrathecal therapy spinal tap cerebral spinal fluids |
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What is chronic lyphocytic leukemia? |
-Affects bcell lymphocytes -most common type of leukemia -almost all over the age of 50 -RAPIDly progresses |
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CLL causes? |
No known Potentially vietnam agent orange |
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Forms of CLL? |
slow-growing (no need for immediate tx, no s&S) Faster growing (needs immediate tx) |
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Staging systems consider certain factors such as: |
-the elevation of your blood and marrow leukemic lymphocyte counts -your lymph nodes size and distribution -your spleen's size -the extent of your decreased blood platelet counts -the degree of anemia |
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CLL Tx? |
-watch and wait -drug therapy (chemotherapy and monoclonal antibody therapy) -white cell (neutrophil) growth factors -Radiation therapy -splenectomy
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Diagnostics w/ leukemia? |
CBC w/ diff -low RBCs, platelets, hub, hct, clotting factos -elevated PTT, WBC w/ immature cells |
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Why do a bone marrow biopsy? |
-identification of blast cells and proteins -chromosome analysis: aids in identification of the type and prognosis |
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Induction stage (stage 1) of chemotherapy |
-supportive care: transfusion, treat infections, use G-CSF and Gm-CSF (stimulate the bone marrow to help produce normal blood cells), granulocytic growth factor of colony stimulating factors -intense phase |
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Consolidation (stage 2) of chemotherapy |
-eliminate residual leukemic cells -multiple cycles, lower dosages |
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What is radiation? |
-damages cellular DNA -Responds quickly to radiation and prevents cells from dividing -systemic radiation is hard on the body |
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What are the types of bone marrow transplant/stem cell transplant? |
Autologous: receive own stem cells (not common) Allogeneic: receive cells from closely matched sibling or unknown donor Syngeneic: cells from identical twin |
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Stage 1 of bone marrow transplant: stem cell obtainment |
-find best match -Three sources: bone marrow harvest, peripheral blood (stem cell pheresis), umbilical cord blood |
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Stage 2 of bone marrow transplant: conditioning regimen |
-lasts 5-10 days -same side effects as with chemo/radiation (nausea, vomiting, stomatitis, capillary leak syndrome, diarrhea, severe bone marrow suppression)
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Stage 3 of bone marrow transplant: transplantation |
-2 days after conditioning stopped, allows chemo drugs to get out of system so they won't kill transplanted cells -WBC close to 0 -infusion like blood transfusion (over about 30 min) |
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Stage 4 of bone marrow transplant: engraftment |
"wait and see what happens" =8-12 days for peripheral blood -12-28 days for bone marrow -when engraftment occurs, know that it worked, rise in blood cell counts -GCSF and GMCSF given to stimulate production |
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Stage 5 of bone marrow transplant: post transplantation recovery |
-waiting period to see level of success -at extreme risk for bleeding and infection
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Complications of bone marrow transplant |
-failure to engraft -graft versus host disease (bone marrow that is transplanted doesn't recognize host) autoimmune disease
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*Presence of what indicates engraftment? |
GVHD |