Anatomy and Cancer Flashcards

1
Q

Define tumour, neoplasm and cancer?

A

Tumour = general term for any swelling in any part of body, can be benign or malignant.
Neoplasm = any abnormal mass of cells (due to uncontrolled division).
Cancer = malignant neoplasm.

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2
Q

Differentiate between malignant and benign neoplasm.

A

Benign | Malignant |
| — | — |
| Innocent behaviour | Aggressive behaviour |
| Localised lesion | Can invade local tissues |
| Can affect surrounding tissue by mass effect (compression NOT invasion) | Can spread to other parts of the body (metastasise) |
| Never metastasises | |

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3
Q

What are the 2 basic components of a tumour?

A
  1. Tumour parenchyma = clonal expansion of neoplastic cells.
  2. Supporting stroma = non-neoplastic connective tissue and blood vessels (abundant stroma-desmoplasia).
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4
Q

How are benign tumours classified (broadly)?

A

Benign tumours are broadly classified based on their cell origin:
- From mesenchyme = benign mesenchymal tumour.
- From epithelium = benign epithelial tumours (based on microscopic or macroscopic elements).

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5
Q

Give examples of benign mesenchymal tumours.

A

Fibroma, osteoma, leimyoma, angioma.

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6
Q

Give examples of benign epithelial tumours.

A

Adenoma, cyst adenoma, papiloma, polyp.

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7
Q

How are malignant tumours classified (broadly)?

A

Also based on their cell of origin:
- From epithelial cells = carcinoma.
- From mesenchymal cells = sarcoma.
Some have more than one parenchymal cell type:
- Mixed tumours = derives from a single germ cell layer that differentiates into more than one cell type.
- Teratomas = derived from more than one germ cell layer and hence composed of many parenchymal cell types.

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8
Q

Describe the major tumour classifications.

A

Classification depends on clinical behaviour & morphological evaluation.
Categorised based on:
- Degree of differentiation (how close the cancer cell is to a normal cell - look at size, shape, nuclear content, polarity etc).
- Growth rate (fast vs slow growing tumours).
- Local invasion (benign vs malignant).
- Metastasis (can colonise distal structures).

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9
Q

Describe the relationship between growth rate and rate of differentiation.

A

Degree of differentiation and growth rate are inversely proportional - if growth rate is too fast the cell won’t have time to differentiate and vice versa.

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10
Q

What are the 3 main ways cancer can spread?

A
  1. Direct extension/local spread.
  2. Lymphatic spread.
  3. Haematogenous spread.
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11
Q

Describe direct extension/local spread.

A

Tumour extends directly into surrounding spaces.
Invasion of adjacent structure/organs.
Seeding:
- Detachment of cells from primary tumour, spread to surrounding structures.

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12
Q

Give an example of direct local invasion.

A

Lung cancer → thoracic wall, mediastinum, root of neck.
Bladder cancer → prostate, rectum, uterus, vagina, pelvic side walls.

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13
Q

Give an example of seeding spread.

A

Peritoneal spread.
Common primaries (primary tumour):
- Gastrointestinal cancers = oesophageal, gastric, colorectal, pancreatic.
- Ovarian cancer.

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14
Q

What is lymph?

A

Interstitial fluid or the fluid lost from capillary bed.

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15
Q

Describe the pathway of lymph.

A
  1. Fluid flows into sinusoids = lymphatic capillary plexus.
  2. These capillary plexuses come together to form lymphatic vessels (continuous endothelial lining).
  3. Superficial vessel drain into deep vessels which drain into large lymphatic vessels which drain into lymphatic trunks.
  4. Both drain into the vena cava.
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16
Q

Where do the 2 main lymphatic trunks drain?

A

Right lymphatic trunk → right venous angle.
Thoracic duct → left venous angle.

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17
Q

What part of the body does each trunk drain?

A

Right lymphatic trunk = right upper limb, right part of trunk & head & neck.
Thoracic duct = rest of body.

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18
Q

What makes up the venous angle?

A

Junction of internal jugular vein and subclavian vein.

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19
Q

Describe the lymphatic spread of cancer.

A

Cells detach from primary tumour.
Enter lymph capillaries draining adjacent tissues (no functional lymphatics within actual tumour tissue).
Colonise distant tissues - lymph nodes.

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20
Q

What is the first lymph node/group of lymph nodes which cancer spreads to known as?

A

Sentinel lymph nodes = first lymph node/s draining a tumour.

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21
Q

What are sentinel lymph nodes used for?

A

Used to predict the likelihood of tumour spread (staging).
Identify sentinel node & take a biopsy.

22
Q

Example of sentinel lymph nodes.

A

Commonly used to help stage disease in: breast cancer, colon cancer, melanoma.

23
Q

What is the sentinel lymph node for breast cancer and how is it identified?

A

Primary lymph node drainage for breast cancer = axillary lymph nodes.
Identify sentinel lymph node by:
- Blue dye (methylene blue).
- Radioactive tracer (Tc 99).

24
Q

What is haematogenous spread?

A

Spread through blood vessels.

25
Describe haematogenous spread.
Cells detach from primary tumour. Enter blood vessels draining tissue. Colonise distant tissues e.g. liver, lung, bone, brain.
26
Where is haematogenous spread most commonly deposited?
Liver, lung, bone, brain.
27
Examples of haematogenous spread.
The liver: - Structures drained by portal venous system primarily metastasise to the liver. The lungs: - Structures drained by systemic venous system enter right circulation via SVC/IVC. The bones: - Common cancers that metastasise to bone include breast, lung, thyroid, kidney, prostate.
28
Why should normal anatomy be known/considered when looking at cancer?
Consider normal anatomy first so you can answer the following: - How might the tumour impact on the normal anatomy of the region? - What is the normal histology vs cancer histology? - How might the tumour spread? - How will knowledge of anatomy influence investigation? - How will knowledge of anatomy influence treatment?
29
What is the anatomical impact of a tumour?
Consider anatomical relations, blood supply, lymphatic drainage, nerve supply, and normal histology.
30
Why should normal anatomy be known when looking at cancer?
To understand how the tumour might impact normal anatomy, its histology, and potential spread.
31
How might a tumour spread?
Locally, via lymphatics, or haematogenously.
32
What are the implications of adjacent structures being compromised?
It may indicate local spread of the tumour.
33
How does knowledge of blood supply influence cancer treatment?
It helps predict the pathway for haematogenous spread.
34
What role do sentinel lymph nodes play in cancer?
They help predict the pathway for lymphatic spread.
35
What symptoms can nerve compression or infiltration cause?
Compression can cause pain, while infiltration can cause paraesthesia.
36
What is the investigative pathway for cancer diagnosis?
1. Clinical assessment (history & physical examination) 2. Imaging (endoscopy, cross-sectional imaging) 3. Pathology (biopsy, excision).
37
What are the three types of intervention once cancer is diagnosed?
Chemotherapy, radiotherapy, and surgery.
38
What does treatment for cancer depend on?
It depends on the stage and type of cancer.
39
What is the treatment approach for local cancer?
Surgery and radiotherapy.
40
What is the treatment approach for haematogenous cancer?
Surgery and chemotherapy.
41
What is the treatment approach for lymphatic cancer?
Surgery and radiotherapy.
42
What is the treatment approach for nerve-involved cancer?
Surgery.
43
What does the scan show in the case study?
An abnormal mass spreading into the floor of the orbit, nasal cavity, and maxilla.
44
What is the diagnosis in the case study?
Maxillary sinus tumour.
45
What are the anatomical relations affected by the maxillary sinus tumour?
Eye, nasal cavity, fossae, floor of orbit, wall of nasal cavity, maxillary molars, and pterygopalatine fossa.
46
What is the blood supply involved in the maxillary sinus tumour?
Sphenopalatine vein, pterygoid plexus, posterior superior alveolar artery, and infraorbital artery.
47
What is the lymphatic drainage for the maxillary sinus tumour?
Submandibular lymph nodes.
48
What nerves are involved with the maxillary sinus tumour?
PSA, MSAN, ASAN, ION.
49
What is the normal histology of the maxillary sinus?
Ciliated pseudo stratified columnar epithelium.
50
What is the histology of the tumour in the case study?
SCC adenocarcinoma.