Lec 14 - Lymphoid Malignancies Flashcards

(35 cards)

1
Q

3 major underlying principles of lymphoid malignancies

A
  • share many characteristics with normal lymphocytes as they arise from normal cells
  • depedning on what stageof developmetn the malig cell is deribed from, they resemble cells at that stage
  • behave differently due to there being so many of them, but also unusual features
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2
Q

4 types of malig cells in terms of developmetal stage

A
  1. from initial lymphocyte production stage
  2. from cells responding to antigen
  3. from cells that have met antigen
  4. from memory cells
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3
Q
  1. where
A

in bone marrow, highly proliferative

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4
Q
  1. appearance of cell
A
  • big nucleus and nucleous = unravelled
  • blue cytoplasm = packed with ribosomes
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5
Q
  1. name of cells at this stage
A

acute lymphoblastic leukemia

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6
Q
  1. where does it grow initially
A
  • at first = edge of bone marrow, resembling normal cells
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7
Q
  1. later behaviour of these cells
A
  • grow rapidly, dont mature
  • fill bone marrow, eliminates all fat spaces
    = supress grwoth of normal cells
  • after filling marrow entirely, will spill over to other areas e.g. the blood
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8
Q
  1. what causes the symptoms
A
  • suppression of normal cell production
  • growth in bone marrow = bone pain
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9
Q
  1. common symptoms
A
  • bleeding (lack of platelets)
  • infection (lack of WBCs)
  • anemia of diff types
  • bone pain
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10
Q
  1. how does its effects change depending on age
A
  • children = behaves like adult disease, but mutations mean more sensitive to treatment
  • elderly = many diff mutations, poor response to treatmenr
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11
Q
  1. which mutation, that is often seen in myeloid leukemias, can be seen is ALL
A

BCR/ABL mutation
used to be hard to treat but new treatment means its now curable

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12
Q
  1. where
A

lymph nodes
this is after meeting an antigen, they go here to proliferate

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13
Q
  1. why variable in visibility
A
  • initially cells vry proliferative = more like bone marrow cells
  • later look like effector cells, less proliferative (still in lymph glands)
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14
Q
  1. appearnace of lymph node
A
  • filled with malignant cells
  • enlarged
  • less variability of cells
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15
Q
  1. name of cells that develop from this stage
A

lymphoma

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16
Q
  1. how can it be traced
A

PET scan
can be seen in lymph nodes
and small amount in kidnet bladder as its excreted

17
Q
  1. why is Burkitt lymphoma special
A

MYC gene is mutated
(usually controls cell division progression)
= makes cells continually proliferate
= one of fastest growing malignancies

18
Q
  1. what stage do these cells arise from
A

effector cells
that leave the lymph glands, and travel through blood to get to bone marrow (where they grow)
(mainly plasma cells ie antibody producing cells)

19
Q
  1. appearance of these cells
A
  • dense chromatin, most is inactive and wrapped around histone (only antibody protein is made)
  • large pale area where the golgi body is = nucleus pushed to one side
  • blue cytoplasm = lots of ribosomes
20
Q
  1. name
21
Q
  1. avg normal amount of antibodies
22
Q
  1. amount of antibodies in myeloma
23
Q
  1. how plasma cell myeloma cause disease
A
  1. excess antibody = sticky = block kidneys, plasma hyperviscosity
  2. abnormal plasma cells displace normal plasma cells = infection
  3. plasma cells make cytokines = holes in bones, fractures, high Ca in bone
24
Q
  1. symptoms
A
  • bone pain and fractures
  • kidney failure
  • effects of slow circulation
  • high rate of infection, reactivation of diseases e.g. shingles
25
4. arise from what type of cell
memory cellls
26
4. where
migrates widely between nodes, blood and tissue in lots of diff tissues
27
4. name
chronic lymphocytic leukemia
28
4. appearance
- nucleus is dense, no nucleolus - pale blue, few ribosomes
29
4. problem wiht these cells
- slow progressive proliferation - survive in excess number - migrate widely
30
4. common way of being diagnosed
routine blood test = raised numbe rof abnormal lymphocytes in blood
31
4. other symptoms of this
- widespread enlargement of lymph glands (slow, painless, usually symmetrical) - bone marrow failure - immune deficiency (but because cells are moslty inert, symptoms are minimal)
32
4. most common cause of death
- immunosuppression = chonic ill health
33
4. autoimmune effects
autoimmune destruction of red cells vry common - severe anaemia
34
4. treatment used
combination of cancer drugs = FCR chemotherapy
35
4. what mutation causes hairy cell leukemia
mutation of BRAF gene - also a malignancy of memory cells