Test 2 - pathology Flashcards

(35 cards)

1
Q

Define grade and what it means to be low, intermediate, and high grade.

A

grade tells you how much the cancer looks like the original cell; differentiation

Low = resembles normal tissue (well differentiated)

intermediate = somewhat resembles normal tissue

High = does not resemble the normal tissue (poorly differentiated)

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2
Q

Is an in-situ carcinoma cancer?

A

No! To be cancer, it must invade the basement membrane

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3
Q

What is TNM staging?

A

Tumor, Node (lymph), Metastasis

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4
Q

What is an in-situ neoplasia?

A

Clonal overgowth of cells which have the potential to invade but have not yet done so

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5
Q

What is a carcinoma?

A

malignant neoplasm derived from epithelial cells

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6
Q

What should trigger you to think someone has a familial cancer syndrome?

A

Young age

rare/uncommon cancer

more than one type of cancer in one person

family history of rare/uncommon cancers

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7
Q

In Von Hippel Lindau disease, what chromosome is mutated? What does the vHL gene regulate?

A

chromosome 3

Hypoxia Inducible Factor

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8
Q

In Von Hippel Lindau disease, what do patients develop? Where?

A

Hemangioblastomas

Medulla, retina, and cerebellum

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9
Q

In Von Hippel Lindau disease, what are patients at increased risk for?

A

cysts in the pancreas, liver, and kidneys

bilateral renal carcinoma

pheochromocytoma

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10
Q

What is the major issue with retinoblastoma?

A

mutation in Rb allows for cell cycle to progress forward

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11
Q

How can retinoblastima be diagnosed with physical examination?

A

leukocoria

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12
Q

What is the major issue with lynch syndrome?

A

defective DNA mismatch repair gene

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13
Q

How is lynch syndrome inherited?

A

autosomal dominant

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14
Q

What are patients with lynch syndrome at high risk for developing (types of cancer)?

A

colon cancer

skin cancer

ovarian cancer

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15
Q

What is the major issue with Li Fraumeni?

A

Mutation in P53

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16
Q

How is Li Fraumeni inherited?

A

autosomal dominant

17
Q

What types of cancer are patients with Li Fraumini at risk for?

A

Breast

Brain

Sarcomas

Leukemias

Adrenalcortical carcinoma

18
Q

What type of cells make embryonic tumors?

19
Q

What do blastomas have a tendancy to do depending on its environment?

A

Blastomas like try and differentiate towards the surrounding cell types (they like to try and look like its surrounding tissue)

20
Q

What is a neuroblastoma? What gene is typically mutated?

A

embryonic cancer of the adrenal glands

N-myc is typically mutated

21
Q

Can you tell what type of cancer this is just by looking at it?

A

No! Although this is a neuroblastoma, all blastomas look the same under the microscope

22
Q

What are the 3 main good prognostic features in neuroblastoma?

A

age < 1 year old

N-myc is not expressed/amplified

clinical stage 1, 2, 4s

23
Q

What embryonic malignancy is this?

(normal image is on the right)

A

Wilm’s/nephroblastoma

24
Q

This slide is triphasic. What is the embryonic maligancy?

A

Wilm’s tumor/nephroblastoma

The blast cells in the middle are trying to look like their surrounding

25
Is Wilm's tumor associate with congenital malformations?
Yes
26
What is WAGR syndrome?
WAGR syndrome is a congenital malformation: **W**ilm's **A**niridia **G**enital anomalies **R**etardation
27
What is medulloblastoma?
embryonic malignancy that typically arises in the cerebellum
28
How does medulloblastoma spread?
Through the CSF
29
What is the term for this clinical finding? What embryonic malignancy causes this?
sunburst pattern osteosarcoma
30
What is this cancer?
osteosarcoma malignant osteoblasts lay down malignant osteoid
31
Where in the bone does osteosarcoma tyically present (epiphysis/metaphysis/diaphysis)
metaphysis
32
Are sunburst patterns seen here?
no
33
What is Ewing's sarcoma mutation?
t(11;22) in primitive neural cells
34
What CD marker do Ewing's sarcoma cells express?
CD99
35
Where do Ewing's sarcoma tumors typically present? (epiphysis/metaphysis/diaphysis)
diaphysis