12 - Neoplasia 1 Flashcards

1
Q

What is a neoplasm?

A

An abnormal growth of cells that persists after the internal stimulus is removed

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2
Q

What is a malignant neoplasm?

A

An abnormal growth of cells that persists after the internal stimulus is removed and invades surrounding tissue with potential to spead to distant sites

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3
Q

What is a tumour?

A

Any detectable lump or swelling, only cancer when it is a malginant neoplasm

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4
Q

What is a metastasis?

A

A malignant neoplasm that has spread from its original site to a new non-contigous site. The original site is the primary site and the place that it spread to is the secondary site

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5
Q

Is dysplasia a neoplasm?

A

No it is a pre-neoplastic alteration with disordered tissue structure, changes are reversible not irreversible like neoplasia

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6
Q

What are the differences between benign and malignant neoplasms macroscopically?

A

Malignant: irregular outer margin and shape, may have areas of necrosis and ulceration, have the potential to metastasise

Benign: grow in a confined local area so have a pushing outer margin, do not metastasise

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7
Q

What is the difference between benign and malignant neoplasms microscopically?

A

Benign: cells are like parent tissue so they are well differentiated

Malignant: can range from well to poorly differentiated, if not resemblance to any tissue they are called anaplastic

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8
Q

What happens to cells microscopically as differentiation worsens? i.e becomes malignant

A

- Increased nuclear size

- Increased nuclear to cytoplasmic ratio

  • Increased nuclear staining (hyperchromasia)

- More mitotic figures

- Pleomorphism (increasing variation in size, shape and staining of cells and nuclei)

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9
Q

What does grading cancer refer to?

A

How differentiated the tumour is, the higher the grade the poorer the differentiation

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10
Q

How are different types of dysplasia classified?

A
  • Dysplasia is reversible altered differentiation
  • Mild, moderate and severe dysplasia, severe meaning worse differentiation and can lead to cancer
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11
Q

What is neoplasia caused by?

A

- Accumulations of mutations in somatic cells = PROGRESSION

- Initiators (mutagens) and Promoters (promote cell proliferation) induce mutations

  • Need single initiator and prolonged promoter exposure to produce a mutant cell population
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12
Q

How do we know that neoplasms are monoclonal?

A
  • In heterozygous females for G6PDH (x-linked) that codes for different isoenzymes
  • In women, one X chromosome undergoes lyonisation, random in each cell
  • In neoplastic tissue all of the cells produce the same isoenzyme, whether heat stable or labile, socome from same cell
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13
Q

Is a persons risk of cancer more down to intrinsic or extrinsic factors?

A

Migrating Japanese

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14
Q

What are some examples of initiators and promoters?

A
  • Chemicals, infections, radiations and inherited mutations are initiators, some can also be promoters
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15
Q

What is progression, in terms of neoplasia?

A

When a neoplasm forms from a monoclonal population due to an accumulation of mutations in critical genes

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16
Q

In neoplasm, what are the two main types of genes that can affect their formation?

A

- Tumour supressor genes: normally supress neoplasm formation so when inactive neoplasm forms. recessive so both need mutating.

- (Proto) Onco-genes: abnormal activation favours neoplasm formation, dominant.

17
Q

What are the general rules of naming neoplasms?

A
  • Neoplasm’s site of origin
  • If malignant or benign
  • Type of tissue tumour forms
  • Gross morphology (e.g cyst or papilloma)
18
Q

What would be the suffix for a benign and malignant neoplasm?

A

Benign: -oma

Malignant: if epithelial -carcinoma (in-situ or invasive depending on basement membrane), if stromal -sarcoma

19
Q

What type of neoplasms are leukaemia and lymphoma?

A

Leukaemia: malignant neoplasm of blood-forming cells arising in the bone marrow

Lymphoma: malignant neoplasms of lymphocyes, mainly in lymph nodes

20
Q

What are germ cell neoplasms and -blastomas?

A

Germ cell: arise from pluripotent cells in the ovary or testis

Blastoma: occur mainly in children from immature precursor cells, e.g nephroblastoma

21
Q

What is a papilloma?

A
  • A papilloma is a benign epithelial tumor growing exophytically (outwardly projecting) in finger like projections
  • Wart like growth on mucous membranes and skin
22
Q

What are some of the different types of polyps?

A
23
Q

Which type of cancer is most likely to form in the following organs:

  • Bladder
  • Bowel
  • Skin
  • Lung
  • Breast
A

- Bladder: transitional cell carcinoma

- Bowel: adenocarcinoma

- Skin: squamous cell carcinoma, malignant melanoma, basal cell carcinoma

- Lung: adenocarcinoma, squamous cell carcinoma, small cell carcinoma

- Breast: adenocarcinoma

24
Q

Which type of cancer is most likely to occur in the following organs:

  • Prostate
  • Brain
  • Pancreas
  • Uterus
  • Oesophagus
  • Stomach
  • Thyroid
  • Cervix
A

- Adenocarcinoma: prostate, pancreas, uterus, oesophagus, stomach, thyroid, cervix

- Squamous cell carcinoma: cervix, oesophagus

- Astrocytoma: brain

25
Q

What are the names of benign neoplasms in the following tissues?

A
26
Q

What are the names of malignant neoplasms in the following tissues?

A
27
Q

What are some benign mesenchymal tumours?

A
  • Lipoma, Leiomyoma
28
Q

What is Hodgkin’s lymphoma and how can it be recognised microscopically?

A

Abnormal B-lymphocytes

29
Q

What is teratoma and how can you recognise it microscopically?

A
  • They typically form in the ovaries and testicles and they are tumours made of several different types of tissue, such as hair, muscle, or bone.
  • Have lots of different cell types and may appear lobulated, with cysts of mucinous or serous material
30
Q

What are some examples of germ cell tumours?

A
31
Q

What is malignant melanoma and how can it be microscopically recognised?

A
  • Malignant neoplasm of melanocytes
  • Same features as normal malignant cells
32
Q

How can squamous carcinoma and adenocarcinoma appear microscopically?

A

SCC: keratin pearlys, hyperchromatic nucleus, angular nuclei and cell shape, pleomorphism

Adenocarcinoma: Unlike squamous cell carcinoma, adenocarcinoma usually does not form a cavitary lesion.

Adenocarcinoma may present as a diffuse pleural thickening resembling malignant mesothelioma.

33
Q

What is different about neuroendocrine tumours and where do they normally affect?

A
  • Always malignant
  • Mainly in GI and respiratory
34
Q

What are some syndromes that neuroendocrine tumours can cause and why?

A

Secrete excess secretory products

- Zollinger Ellison Syndrome: pancreatic and gastric tumours producing too much gastrin

- Cushing Syndrome: excess corticotrophin secretion

- Carcinoid Syndrome - collection of symptoms some people get when a neuroendocrine tumour, usually one that has spread to the live

35
Q

What is carcinoid syndrome and what symptoms does it cause?

A
  • Neuroendocrine tumour mainly seen with liver metastases
  • Excess secretion of serotonin as well as other products like histamine, prostaglandin, bradykinin

- Symptoms: flushing, products in urine and blood, ab pain, diarrhoea, nausea and vomiting

36
Q

How are GI endocrine tumours graded?

A

Grade 1 and 2: well differentiation neuroendocrine

Grade 3: poorly differentiated neuroendocrine

37
Q

How are neuroendocrine tumours in the respiratory system graded?

A
  • Lower grade malignant tumours (typical and atypical carcinoids) to high grade carcinomas
  • Presences of necrosis and mitotic activity is key
38
Q

What markers may neuroendocrine tumours have on their surface?

A
  • Synaptophysin
  • Chromogranin
  • CD56

Graded by TNM system