W3: Leukaemias, Lymphomas and Myelomas Flashcards

(52 cards)

1
Q

define leukaemia

A

cancer of wbcs

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2
Q

define lymphoma

A

cancer of lymphoid tissue

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3
Q

define myeloma

A

cancer of clonal plasma cells in BM (B cells)

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4
Q

4 main types of leukaemia

A

Acute myeloid leukaemia (AML)
Acute lymphoblastic leukaemia (ALL)
Chronic myeloid leukaemia (CML)
Chronic lymphoid leukaemia (CLL)

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5
Q

2 types of lymphoma

A

Hodgkin’s
Non-Hodgkin’s

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6
Q

2 cell cycle abnormalities that cause cancer + where do they occur

A

mutations in proto-oncogenes

mutations in tumour suppressor genes

occurs in BM or peripheral lymphoid tissue

*mutation in single gene

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7
Q

incidence vs prevalence

A

i = rate of new cases in given time period/ % of pop at risk of dev

p = no. of people already w condition

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8
Q

known causes of leukaemia

A
  • previous chemotherapy w alkylating agents
  • radiation exposure
  • benzene/ formaldehyde exposure
  • genetic conditions (down’s syndrome)
  • myelodysplasia (pre-leukaemia)
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9
Q

dysplasia vs myelodysplasia

A

d = abnormal dev
md = abnormal dev of myeloid cells (pre-leukaemia)

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10
Q

define acute myeloid leukaemia

A

> 20% myeloblast cells (immature wbcs) in blood/ BM

affects myeloid line (granulocytes + monocytes)

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11
Q

define acute lymphoid leukaemia

A

> 20% lymphoblast cells (immature wbcs) in blood/ BM

affects lymphoid line

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12
Q

define chronic myeloid leukaemia

A

chronic = incr no. of mature cells than blast cells

affects myeloids (granulocytes + monocytes)

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13
Q

define chronic lymphoid leukaemia

A

chronic = incr no. of mature cells than blast cells

affects lymphocytes

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14
Q

AML: median age

A

60yrs

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15
Q

AML: signs + symptoms + why

A
  • Acute, often critically ill
  • Malaise, fever, sweats (high E use of uncontrolled prolif - hot + sweaty)
  • Symptoms of anaemia (BM too crowded so no space + nutrients to make rbcs)
  • Neutropenia - infections
  • Thrombocytopenia - bleeding / DIC
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16
Q

what type of anaemia can be seen in AML + why

A

normocytic normochromic bc nothing wrong w prod of rbcs just not enough space to make them

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17
Q

testing to distinguish btwn myeloid leuk vs lymphoid leuk

A

m = myeloperoxidase (MPO) pos (enzyme found in granulocytes)

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18
Q

prognosis of AML

A

chemo leads to complete remission in 80-90% younger patients
cure rate lower ~45%

older patients - 5yr survival rate ~15%
cure rate rare

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19
Q

define “in remission”

A

cancer repressed to <5% blast cells

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20
Q

chemotherapy side effects

A

chemo = cytotoxic drugs = toxic to all rapidly dividing cells (healthy or not)

side effects:
- hair loss (bc hair follicles divide fast)
- nausea + vomiting (bc mucus mem gut lining cant divide)
- decr in sperm prod -> infertility

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21
Q

ALL: peak age, % of childhood leukaemias, ratio caused by B to T cells, categories

A

0-4 yrs
80%
85:15
L1-L3

22
Q

ALL signs + symptoms

A
  • Starts abruptly
  • Bone + joint pain
  • Symptoms of BM failure (anaemia, infection, haemorrhage)
  • Generalised lymphadenopathy (enlarged lymph nodes in multiple places)
    Hepatosplenomegaly (liver + spleen reactivated to prod wbcs)
  • Testicular involvement
  • CNS manifestations
23
Q

define sanctuary site

A

places in body where chemo struggles to reach

24
Q

ALL blood test

A

leukocytosis/ leukopenia/ normal wbc count

normo, normo anaemia

neutropenia
thrombocytopenia
wbcs MPO neg

25
ALL prognosis
children curable w chemo + CNS prophylaxis adult cured less freq - stem cell transpalnt 35% 5y survival adults
26
CML common age range
65-85 yrs
27
CML associated w presence of which chromosome
Philadelphia
28
CML S+S
fatigue, weight loss, sweaty splenomegaly hepatomegaly (sensation of fullness) gout, bruising leukostasis (clumping of leukocytes)
29
CML blood test
leukocytosis, neutrocytosis incr basophils normo normo anaemia thrombocytosis most freq incr lactate dehydrogenase (LDH)
30
CML prognosis
50% 5y survival indolent (slothful), followed by period of acceleration + final generally fatal leukemic phase stem cell transplant - can cause mortality tyrosine kinase inhibitor - imatinib as initial therapy
31
CLL age
50+ , peak at 90+
32
CLL S+S
asymptomatic symmetrical + painless enlargement of lymph nodes symptoms of anaemia weight loss indolent
33
CLL blood test
lymphocytosis wbcs appear as small + round lymphocytes smear cells (fragile lymphocytes burst during processing) immunotyping - shows as almost always B cells (bc CD19+ on surface) normo normo anaemia thrombocytopenia
34
CLL prognosis
initially indolent chemo not needed immediately 705 5y survival often die of other causes becomes more aggressive in advanced stages
35
lymphoma is
cancer of lymphoid tissues e.g spleen, lymph nodes, tonsils, adenoids, thymus
36
lymphoma effects
swollen lymphod tisses fileld w B or T cells
37
% ratio of hodgkins vs non-hodgkins lymphoema + which cells + how distinguished
40% H (B lymphs) 60% non-H (T or B lymphs) biopsy node + stain lymphs CD15 marker of Reed-Sternburg cells (in hodgkins)
38
hodgkins lymphoma
Malignant B-cells accumulate in lymph nodes malignant cells = minority of tumour inflammatory cells = majority
39
2 peak ages of hodgkins
15-35 over 50
40
hodgkins S+S
asymmetrical + painless lymphadenopathy (swollen lymph nodes) splenomegaly fever, night sweats, wt loss, pruritus (itching), fatigue in minority
41
hodgkins blood test
normo normo anaemia eosinophilia neutrophilia normal/ incr platelet count advanced disease - lymphopenia, thrombocytopenia
42
hodgkins prognosis
80% 10y survival largely determined by stage of disease chemo -> high cure rates risk of 2ndary malignancy as late side effect of treatment
43
non-hodgkins age
85-89
44
non-hodgkins S+S
asymmetrical painless lymphadenopathy Less fever, night sweats + wt loss than w Hodgkin’s Sore throat Symptoms of anaemia/ thrombocytopenia/ neutropenia w infections Acute abdominal symptoms due to spleen/ liver enlargement + involvement of GI tract
45
non-hodgkins blood tests
normo normo anaemia - maybe autoimmune haemolytic anaemia in advanved diseas w marrow involvement - neutropenia, thrombocytopenia lymph node biopsy cytogenics (chromosome mapping)
46
non-hodgkins prognosis
55% 10y survival indolent chemo effective cure elusive aggressive NHL cured w chemo + ruiximab stem cell transplant
47
multiple myeloma (MM)
cancer of clonal plasma cells in BM (B cells)
48
MM detected by
Ab secreting B cells that secrete paraprotein (aka M protein) (detectable in serum/ urine)
49
MM age + race most effected
85-89 african americans
50
MM S+S
bone pain, fractures anaemia symptoms thrombocytopenia leukopenia renal failure, hypercalcaemia amyloidosis (deposition of abnormally folded proteins)
51
MM blood tests
incr plasma cells in BM presence of paraprotein normo normo OR macro anaemia pancytopenia hypercalcemia
52
normo