Leukemias Flashcards

(66 cards)

1
Q

Acute leukemia

A

Abnormal proliferstion of precursors

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2
Q

Chronic leukemia

A

Abnormal proliferation of mature cells

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3
Q

L stands for

A

Lymphoblasts

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4
Q

M Stands for

A

Myeloid line of stem cells

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5
Q

Most of our lymphocytes are

A

B cells

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6
Q

AML

A

Acute myelobkastic leukemia, bunch of myelobkasts precursors

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7
Q

Myelogenous or myelobkastic

A

Mature myeloid cells proliferating

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8
Q

ALL

A

Acute, in bone marrow or precursors, abnormal of lymphoblasts, all that exists I. Bone marrow are lymphoblasts. No room for myeloid line to proliferate. So deficiency in myeloid cells, some red blood cells but so squeezed that get liched off on way out of bone which look like tear drop.

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9
Q

Thrombocytopenia shows as

A

Superficial bleeding, increased bleeding tume

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10
Q

ALL occurs in

A

Children

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11
Q

AML

A

Myeloid are abnormally proliferating, crows out bc so li has off as exiting so tear drops cells, those myeloid blasts NEVER differentiate into normal cells so you get petechial bleeding.

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12
Q

Fever, night sweats, petechial bleeding, bone pain, hepatisplenomegaly, enlarged Ln

A

Leukemia patients

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13
Q

Greater than 30% lymphoblasts in blood, children

A

ALL

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14
Q

Chrom deletion or somatic hyoermutation, scant cytoplasms, hepatosplenomegaly, Lymohocytosis (lots of lymphocytes), 20-30% have thrombocytopenia,, male adults (average age of Dx is 70 years old)

A

CLL

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15
Q

AML

A

Acute, bone marrow, myelobkastic proliferate, the myeloblasts differentiate into something that proliferates. Ex, an erythroblasts proliferates. auer rods are pathognomonic. Echymosis, petechial. Greater than 30% myelobkasts. Occurs in adults (average age is 67) range is from 0 to elderly.

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16
Q

CML

A

Myelogenous line is abnormally proliferating, Philadelphia chromosome, hypecelukar marriw, elevated eosinophils and basophils, massively increased WBC count (more than 200k), mature myeloid are seen in periphery, average age is 60-65

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17
Q

Auer rods

A

AML

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18
Q

Azurophikic granular material forming elongated needles in cytoplasm of leukemia blasts

A

Auer rods in AML

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19
Q

Sudan strains for

A

Fat

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20
Q

Sudan black stains positive in

A

Myeloblasts for AML

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21
Q

Translocation for AML variant M3

A

Translocation 15;17

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22
Q

Blast cells are seen in

A

ALL

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23
Q

Most common pediatric malignancy

A

ALL

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24
Q

TDT, Cd10 and CD19

A

B- ALL

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25
Cd1a, cd2, cd3, cd4, cd5, cd7 y cd8
T-ALL
26
ALL stain positive for
PAS, stains the carbohydrate macromolecules
27
SVC Syndrome
Enlarged head, flushing, vision issues, could have upper extremity edema if it is at the brachicephalic junction.
28
Stridor
Louder and high pitched than whiz. Sounds like a whistle. When you breath in.
29
Inspiratory whiz
Airway compromise.
30
Why does AML carry a worse prognosis than ALL?
Because person can not generate neutrophils or macrophages
31
Methotrexate is used for which one? ALL or AML?
ALL
32
Monocytes, macrophages, neutrophils proliferate
CML
33
CML originate in the ———— and not in the ———
Periphery, bone marrow
34
Blast crisis
Reverts back to being acute leukemia so you’d see greater than 20% blasts in blood and it can be myelobkasts or lymphoblasts and that can lead to bone pain.
35
Greater than 30% myeloblasts
Acute leukemia
36
Smudge cells
Fragile lymphocytes, with no cell membrane and no nuclear structure, seen in CLL
37
Seen in over the age of 50. Average age of presentation is 70
CLL
38
CLL
Best prognosis because lymphocytes are functional produce antibodies even though* Not at normal amount, but well enough.
39
If WBC in CLL becomes too great, then risk of
Thrombosis because it clogs vessels.
40
If WBC in CLL becomes too great, then risk of ?
Thrombosis because it clogs vessels.
41
Guy in 40s, lymph nodes enlarged. It was huge, and Inside, it was Completely black. No Sx other than that enlarged LN.
Metastatic melanoma from bottom of his foot - acrolentifinous melanoma
42
Most common type of melanoma
Superficial spreading
43
Reed sternberg cells
Hodkin’s lymphoma
44
Cd15 y cd30 positive, muktinucleated cells, cd20 y cd45 negative
Reed sternberg cells, Hodkin’s lymphoma
45
Hodkin’s age of appearance
Bimodal distrobution: 16-44 y more than 55
46
Hodkin’s with Mst RS cells
Mixed cellularity, seen in EBV, HIV and elderly population
47
Overexpression of bcl2 antiapoptotic gene
Follicular lymphoma, t(14;18)
48
Tingible bodily macrophages, a macrophage with a dead tumor cells inside gives the look of a starry sky
Burkitt
49
Children with chronic malaria can suffer from this lymphoma
Burkitt
50
Seen in Africa, big mass in jaw, also distan ileum, cecum, ovaries, kidney
Burkitt
51
Can present as a Bowel obstruction in AIDS patient early on in AIDS.
Burkitt
52
Hemorrhagic cystitis caused by
Cyclophosphamide
53
Cyclophosphamide gets metabolized into ——- which damages the epithelium.
Acroline, which damages the epithelium. causing cystitis
54
To prevent toxicity of cyclophosphamide give
MESNA
55
Bone marrow proliferation can cause primary ——-
Polycythemia Vera
56
Headache, hypertension, hyoercoagulable, vertigo, itchy after hot shower - mast cell degranulation causes pruritis
Polycythemia Vera
57
How to treat polycythemia Vera?
Phlebotomy
58
All cell lines depleted
Aplastic anemia
59
Drugs that cause aplastic anemia
Chloramphenicol, AZT, benzene, vinbkastine
60
Destruction and subsequent scarring of the bone marrow
Myelofibrosis
61
Citrate, found in blood in transfusion, binds to —— in the blood and causes ——
Calcium, hypocalcemia
62
Mephalam
Treats multiple myeloma Alkylation agents
63
PSA
Cancer antigen, prostate
64
CEA antigen
Colon, liver
65
AFP antigen
Yolk sac cancers
66
S-100
Melanoma