Cancer Pathology Flashcards

1
Q

describe the dysplasia-carcinoma sequence

applies to many common carcinomas eg breast, bowel, oesophageal, cervical

A
  • Gradual accumulation of mutations
  • Progression of tumour phenotype
  • Becomes more aggressive - gains invasive and metastatic potential.

Cell w mutation -> hyperplasia -> dysplasia -> carcinoma in situ -> invasive carcinoma -> metastases

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2
Q

Common histological features of dyplasia?

A
  • Cellular pleiomorphism
  • Nuclear pleomorphism
  • Loss of differentiation
  • Architectural disorder
  • Hyperchromatic nuclei
  • prominent nucleoli
  • high N:C ratio
  • frequent and atypical mitotic figures
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3
Q

Features that help distinguish an invasive carcinoma?

A
  • Breach of BM or muscularis mucosa
  • Desmoplastic stroma (including fibrosis)
  • Necrosis (due to outgrowing blood supply)
  • LN involvement/distant metastases
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4
Q

Name 2 histological features that

might help identify a squamous cell carcinoma and 1 that helps identify an adenocarcinoma

A

Sq cell carcinoma: keratin pearls; intracellular bridges

Adenocarcinoma: gland/acinar formation

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5
Q

Which serovars of HPV confer the greatest risk of cervical cancer?

A

serovars 16 and 18

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6
Q

What does a Pap smear involve?

A

Taking a sample of ecto and endocervical cells and performing a cytological analysis

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7
Q

How are cervical cancers graded - cytological grading?

A
  • HSIL (high-grade squamous intraepithelial invasion)
    = HPV infection, mild dysplasia, CIN I
    -LSIL (low-grade squamous intraepithelial invasion)
    = mild to moderate dysplasia, carcinoma in situ, CIN II/II
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8
Q

How are cervical cancers graded - histological grading?

A
Reqs biopsy (colposcopy) to look at cellular histological architecture
CIN = cervical intraepithelial neoplasia

CIN I: mild dysplasia, atypical cells confined to lower 1/3 of epithelium
CIN II: moderate dysplasia, atypical cells in lower 1/2 of epithelium, upper 1/2 cells flattened
CIN III: severe dysplasia and carcinoma in situ, atypical cells in full thickness of epithelium

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9
Q

Examples of important tumour suppressor genes?

A

p53
APC
BRCA1/2

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10
Q

Examples of important proto-oncogenes?

A
RAS
RAAF
Bcr-Abl 
WNT
MYC
ERK
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11
Q

Myeloid cells are those originating from a common myeloid progenitor.
Which cells are they?

A
Monocytes/macs
Neutrophils
Eosinophils
Basophils
Megakaryocytes/platelets
RBCs
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12
Q

Lymphoid cells are those originating from a common lymphoid progenitor. Which cells are they?

A

B cells
T cells
NK cells

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13
Q

What is a leukaemia?

A
  • typically presents w diffuse bone marrow involvement

- often assoc w peripheral blood involvement

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14
Q

What is a lymphoma?

A

-typically presents as a discrete tissue mass (esp lymph node)

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15
Q

How can lymphoma and leukaemia overlap?

A

Uncommonly in leukaemia, a non-bone marrow collection can be the first presentation

Lymphomas can progress to have bone marrow/peripheral blood involvement like leukaemias

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16
Q

ALL is the most common cancer of children (ave age 3 yrs).

How does it present?

A
Bone pain
Pancytopaenia 
Easy bruising 
Lymphadenopathy
Also freq infections/fever, fatigue dt anemia
17
Q

CLL is the most common leukaemia in adults (ave age 60 yrs). How does it present?

A

Non-specific, indolent presentation
Lymphadenopathy most common feature but often not present
Lymphocytosis of peripheral blood

18
Q

Typical histological features of CLL?

A

Many small atypical lymphocytes

“Smudge cells” - fragile cells collapse during film preparation

19
Q

Features of Hodgkin’s lymphoma?

A
  • typically localised to a single axial group of LNs
  • orderly pattern of contiguous spread, from one LN group to the next
  • rarely involves mesenteric LNs, or Waldeyer’s ring
  • rarely presents extra-nodally
20
Q

Features of non-Hodgkin lymphoma?

A
  • usually involves multiple LNs at presentation, incl peripheral LNs
  • non-contiguous pattern of spread
  • often involves mesenteric LNs and Waldeyer’s ring
  • extra-nodal presentation not uncommon
21
Q

Major histological feature of Hodgkin lymphoma?

A

Reed-Sternberg cells

large cells, multinucleated or mononuclear but multilobed

22
Q

Major histological feature of AML?

A
  • Auer rods (in cytoplasm)

- cells w bilobed nuclei and granular cytoplasm also suggest AML

23
Q

What is the relation between Bcr-Abl and CML?

A

Bcr-Abl is a fusion protein created by a translocation bn chromosomes 9 and 22.
It is an unregulated tyrosine kinase -> incr signal transduction

24
Q

Blood smear findings in CML?

A

Recognisable, mature neutrophils

25
Q

Main parts/features of a lymph node?

A

Cortex - location of B cells
Paracortex - location of T cells
High endothelial venules - deliver
circulating lymphocytes and antigens into
LN
Follicles - site of stimulation, clonal expansion and maturation of B cells
Medulla - consists of a network of lymphatic sinuses which drain into the efferent lymphatics
Medullary cord - an expansion of cortical cells