Pathology in diagnosis and management Flashcards

1
Q

Why is tumour pathology important?

A

Useful for clinical presentation, classifying neoplasms and determining treatment options.

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2
Q

What are the main gross characteristics of a benign tumour?

A

Well circumscribed
Smooth
Mobile

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3
Q

What the main gross characteristics of a malignant tumour?

A

Irregular
Poorly defined
Fixed to adjacent tissue

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4
Q

What are the two types of breast lumps that can develop?

A

Fibroadenoma - benign glandular neoplasm in women <30. ‘Breast mice’ due to mobility
Breast carcinoma - Malignant neoplasma and commonest cause of female death. >50yrs mainly. Invades local structures

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5
Q

Where do most cases of colon cancer arise and why?

A

Glandular epithelium = adenocarcinoma.
It is the area exposed to the highest concentration of carcinogens and has a high turnover rate, making it susceptible to mutations.

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6
Q

How does cecum or ascending colon cancer present?

A

Often polypoid and rarely causes obstruction.

Weight loss and anaemia from low grdde blood loss

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7
Q

How does sigmoid colon cancer present?

A

Most common site. Stenosing and causes bowel obstruction.

Altered bowel habit, constipation due to hard stool and narrow lumen or diarrhoea as only watery stool passes through.

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8
Q

What specimens can be obtained from a neoplasm and how are they obtained?

A

Biopsy - small piece of tissue from endoscopy or needle / punch biopsy
Cytology specimens - individual or small group of cells from smears, brushing, fluids, FNA
Surgical resection

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9
Q

Why are specimens needed?

A

To confirm diagnosis and identify histology type to plan future treatment.
A surgical resection can be used to see if the resection had good margins.

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10
Q

What is offered to a Pt if metastasis is established?

A

No surgery

Chemo or radiotherapy

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11
Q

What are the limitations of biopsies?

A

Tumours are heterogenous and have varying appearances in different parts so may not select all types.
Targeting the lesion may be difficult do to size or accessibility or near vulnerable/dangerous structures.

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12
Q

Why can pancreatic cancer not be biopsied?

A

Because there is a surrounding stromal reaction occurring at the site, would lead to rapid deterioration and seeding.

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13
Q

What are the advantages and disadvantages of cytology specimens?

A

Obtained via less invasive methods e.g. cystoscopy and FNA uses a thinner needle than biopsy.
Provides access to sites not suitable for biopsy due to thin needle.
Smaller tissue samples but may make interpretation more difficult

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14
Q

Why might a surgical resection be used?

A

With the aim to cure.
Also used in pallative treatment to reduce symptoms.
To determine if further treatment is required and if good margins.

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15
Q

What does a resection confirm?

A

The diagnosis
Aggressiveness and grade of tumour
Extent of spread = staging and node involvement
Resection margins
necrosis or haemorrhage
Micro and macro - shape, size, histology, origin

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16
Q

What does staging show?

A

The extent of spread and therefor determines prognosis.

17
Q

Name three types of staging.

A

TNM
Duke’s system for colorectal
Breast cancer uses T1-T4 for description of invasion into chest wall

18
Q

What increases the stage of cancer if present?

A

Capsular or vascular invasion

19
Q

What data must be included in a histopathology report?

A
Prognostic information
Data for cancer registration
Quality of resection feedback
Adjuvant therapy decision
Evealuate effectiveness of neoadjuvant therapy
20
Q

What is immunohistochemistry?

A

A fluorescently labelled Ig used to identify an Ig bound to an antigen of a cell.

21
Q

How is immunohistochemistry used to estabilish malignancy ?

A

Reactive inflammatory infiltrates will have a mixed population of mostly T and some B cells.
Neoplastic infiltrates with have a PURE population of cells, composed of B cells, showing clonal population

22
Q

How is immunohistochemistry used as a prognostic marker?

A

Show cell turnover

Determines the metastatic potential and grade

23
Q

How is immunohistochemistry used to identify theraputic options?

A

The expression of a specific antigen marker will identify if the tumour is likely to respond to specific targeting therapies that target these antigens.
e.g. HER2 in breast cancer = Herceptin
Oestrogen R in breast = Hormonal Tx

24
Q

What is in-situ hybridisation?

A

A molecular technique that uses probes to recognise specific DNA sequences within tissue sections. Can test for kappa and lamda chains for the presence of plasma cell infiltrates for reactive v neoplastic.
EBV is encoded into RNA

25
Q

What is post-transplant lymphoproliferative disease and what causes it?

A

An abnormal lymphoid proliferation when immunosuppressed. May be due to polyclonal lymphoid hyerplasia or monoclonal malignant lymphoma.

26
Q

Which virus is mostly associated with PTLD?

A

EBV - Virus infects B cells and remains latent under control of T cell response but when imunnosuppressed T cell function is reduced and EBV proliferation within B cells occurs.

27
Q

How does PTLD present?

A

Within 12 months post-transplant with focal masses or diffuse infiltrates.

28
Q

How can extracted RNA or DNA be used in diagnosis?

A

Can identify Ig gene rearrangments ot TCR rearrangement to demonstrate clonality in B and T cell neoplasms. Determines gene mutations and the treatment options.

29
Q

Why is a MDT needed?

A

To make decisions regarding diagnosis, treatment etc using the specialist knowledge from a variety of different HCP.