Week 6 Flashcards

(87 cards)

1
Q

AML

A

acute myeloid leukemia

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2
Q

AML

A

heterogenous clonal stem cell malignancy where immature hematopoietic cells proliferate uncontrollably

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3
Q

AML results in __

A

inhibited hematopoiesis seen in neutropenia, anaemia, thrombocytopenia

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4
Q

AML FAB subtype

A

M0 -7

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5
Q

most common risk factor for AML

A

radiation

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6
Q

what genetic disorder causes AML

A

down syndrome

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7
Q

prognositc indicators of AML

A

age, cytogenetics, molecular genetics

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8
Q

AML chemotherapy

A

idarubicin
daunorubicin
cytarabine
consolidation with HIDAC

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9
Q

targeted therapy AML

A

FLT3 inhibitor
CD33 inhibitor

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10
Q

Acute promyelocytic Leukemia have balanced reciprocal translocation between chromosome __

A

15 & 17

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11
Q

Acute promyelocytic Leukemia is sensitive to __

A

ATRA, anthracyclines, arsenic trioxide

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12
Q

Acute promyelocytic Leukemia complicated by __

A

life threatening coagulopathy

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13
Q

Acute Lymphoblastic Leukemia

A

lymphoid line of blood cell cancers; development of large number of immature lymphocytes

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14
Q

Acute Lymphoblastic Leukemia arises from __

A

lymphoid progenitor cell sustaining significant multiple genetic damage

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15
Q

Acute Lymphoblastic Leukemia chemotherapy

A

multiagent chemotherapy
- induction
- consolidation-intensification
- maintenance

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16
Q

Chronic myeloid leukemia

A

pluripotent hematopoietic stem cell neoplasm

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17
Q

Chronic myeloid leukemia characterized by __

A

BCR-ABL1 fusion gene from balanced translocation between long arms of chromosome 9 & 22

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18
Q

Chronic lymphocytic leukemia present with __

A

lymphocytosis

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19
Q

Chronic lymphocytic leukemia present with symptoms such as __

A
  • lymphadenopathy
  • splenomegaly
  • anemia
  • fatigue
  • recurring infections
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20
Q

Chronic lymphocytic leukemia diagnosis is confirmed by clonality of __

A

circulating B lymphocytes confirmed by flow cytometry

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21
Q

GVHD

A

graft versus host disease

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22
Q

GVHD treatment

A
  • steroids
  • MMF/Cellcept
  • tacrolimus/cyclosporin
  • infliximab
  • extracorporeal photopheresis
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23
Q

GVHD occurs after

A

100 days

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24
Q

areas affected by GVHD

A

skin, mouth, liver, eyes, lungs, gut, joints

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25
lymph nodes at cervical region
posterior, cervical, pre-auricular, upper cervical, median/lower cervical, supraclavicular
26
lymph nodes at axillary region
axillary
27
lymph nodes at epitrochlear
epitrochlear
28
lymph nodes at mediastinal
paratracheal, mediastinal, hilar, retrocrural
29
lymph nodes at para-aortic
para-aortic, common iliac, external iliac
30
lymph nodes at inguinal
inguinal, femoral
31
lymph nodes at popliteal
popliteal
32
lymph nodes at mesenteric
celiac, splenic hilar, portal, mesenteric
33
common lymphoma symptoms
lumps, fatigue, loss of appetite & weight, fever, night sweats
34
diagnostic work-up & staging of lymphomas
biopsy, imaging, BM aspirate & trephine
35
BM
bone marrow
36
diffuse large B cell lymphoma biological prognostic markers
cell of origin, double-hit, molecular subtype
37
CAR
chimeric antigen receptor
38
immunotherapy management consists of
monoclonal antibodies, cellular therapy, immunostimulants, CAR
39
treatment concept
disease factor, patient factor, drug efficacy/toxicity
40
autologous stem cell transplant
1. collection 2. processing 3. cryopreservation 4. chemotherapy 5. infusion
41
CAR T cell therapy
1. leukapheresis 2. t-cell activation/transduction 3. modified T cell expansion 4. chemotherapy 5. modified T cell infusion
42
myoblast forms __
granulocytes = eosinophils, basophils, neutrophils
43
how to differentiate types of cancer
flow cytometry analysis
44
leukostasis causes ___
high blast count > hyperviscosity > decreased tissue perfusion
45
leukostasis affects what systems?
CV, pulmonary, GI, CNS
46
precursor lymphoid neoplasms are __
B & T lymphoblastic leukemia
47
ALL uses multiagent chemotherapy which causes __
- induction - consolidation-intensification - maintenance
48
what is philadelphia chromosome
reciprocal translocation between chromosome 9 & 22 to create BCR-ABL fusion gene; specific to CML cells
49
diagnosis of chronic lymphocytic leukemia is done via ___
peripheral blood
50
stem cell transplant process
preparation > conditioning > stem cell transfusion > engraftment
51
B cell development process starts & ends from
v-region gene recombination > clonal expansion > somatic hypermutation > selection > close switching > differentiation
52
areas inside lymph node
geminal centre, mantle zone, marginal zone
53
hodgkin's lymphoma is what type
precursor B-lymphoblastic leukemia
54
low grade lymphomas
slow growing and remains dormant
55
high grade lymphomas
rapidly growing & aggressive
56
high grade lymphomas mainly target
brain, eye, spinal cord, intestines
57
rare place of lymphoma development
brain, eye, skin
58
burkitt lymphoma
translocation between chromosome 8 with 14
59
staging of non-hodgkin lymphoma is done via __
ann arbor staging
60
ann arbor stages are __
stage 1 = single region stage 2 = 2 or more regions stage 3 = > 2 regions above & below diaphragm stage 4 = widespread
61
diffuse large B cell lymphoma prognostic factors
age, perfusion status, LDH, extranodal site, staging
62
diffuse large B cell lymphoma biological prognostic markers
cell of origin, double hit translocation, molecular subtypes
63
Erythrocyte stimulated by
EPO from kidney in response to tissue hypoxia
64
lifespan of RBCs
120 days
65
types of leukocytes
monocytes, neutrophils, eosinophils, basophils, lymphocytes
66
most common leukocytes
neutrophils
67
leukemias derived from __
immature lymphocytes
68
lymphomas derived from __
mature lymphocytes
69
acute vs chronic leukemia
Abrupt onset with marked sign (persistent infection and excessive bleeding) & symptoms vs. insidious onset with mild signs & better prognosis
70
what diseases causes congestion & enlargment of lymphoid tissue
lymphacenopathy, splenomegaly, hepatomegaly
71
antacids
alkalize urine to prevent uric acid stone formation
72
hodgkin lymphoma is characterized by __
large abnormal B cells
73
hodgkin lymphoma peaks at which stages of life
20 - 30s 60 -70s
74
hodgkin lymphomas commonly affect ___ lymph nodes
cervical, axillary, inguinal, retroperitoneal
75
haemophilia A is due to abnormal ___
clotting factor VIII
76
haemophilia B is due to abnormal ___
clotting factor IX
77
haemophilia C is due to abnormal ___
clotting factor XI
78
Diagnostic test for Haemophilia A include
PTT, APTT & coagulation time prolonged low serum levels of specific clotting factor based on hemophilia type
79
haemopphilia A treatment
o Desmopressin (DDAVP) o Replacement therapy for Factor VIII o Recombinant DNA product (Advate) o Nplate
80
desmopressin is used to __
raise clotting factor levels
81
Nplate is used to stimulate __
platelet production in bone marrow
82
multiple myeloma management includes ___
curative using bone marrow transplant symptoms using CRAB relief
83
CRAB relief stands for __
calcium, renal failure, anemia, bone lesions
84
most critical test for multiple myeloma is __
bone marrow biopsy
85
serum protein electrophoresis is used to look for __
IgG M protein
86
urine protein electrophoresis is used to look for __
bence-jones protein
87
evidences of end-organ damage include
hypercalcemia, renal insufficiency, anaemia, bone lesions