8. Neoplasia 1 Flashcards

(56 cards)

1
Q

Neoplasm

A

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

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2
Q

Malignant neoplasm:

A
  • An abnormal growth of cells that persists after the initial stimulus is removed AND invades surrounding tissue with potential to spread to distant sites
    • Spread – metastasis
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3
Q

Hyperplasia

A

• Is a growth in number of cells but this is a physiological condition, due to an increase in demand

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4
Q

Tumour:

A

• Any clinically detectable lump or swelling. A neoplasm is just one type of tumour.

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5
Q

Cancer:

A

• Any malignant neoplasm.

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6
Q

Metastasis:

A

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

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7
Q

Tumours can be

A

• Non neoplastic = not cancer e.g. dysplasia
• Neoplastic = cancer
○ Benign
○ Malignant
▪ Primary or secondary (metastatic that can spread)

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8
Q

Dysplasia

A
  • A pre-neoplastic alteration in which cells show disordered tissue organisation. It is not neoplastic because the change is reversible.
    • Associated with cancer but doesn’t have to lead to cancer
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9
Q

Benign neoplasms

A
• Benign tumours grow in a confined local area and so have a pushing outer margin. This is why they are so are rarely dangerous. They grow in one area and stay there.
		○ Obstructions, can block things 
		○ Loss or gain of function
		○ Pressure on things like nerves
		○ Create stress or anxiety
		○ Can become malignant
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10
Q

Malignant neoplasm

A

• Malignant tumours have an irregular outer margin and shape and may show areas of necrosis and ulceration (if on a surface). Tumour breaks into pieces and spreads (metastasis = death)
○ Block things like intestines
○ Use a lot of nutrients in cancer cells
○ Destroy organs by invading tissues
○ Bleeding – blood loss

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11
Q

Benign Neoplasms under the microscope

A

• Benign neoplasms have cells that closely resemble the parent tissue, i.e. they are well differentiated.
○ Look very similar to how they should look, still have fucntion

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12
Q

Malignant Neoplasms under the microscope

A

• Malignant neoplasms range from well to poorly differentiated. Cells with no resemblance to any tissue are called anaplastic.
○ Poor differentiation is bad as it doesn’t resemble normal tissue so tissue is completely abnoral

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13
Q

Things to look for in tumour cells

A

—> With progressing differentiation individual cells have increasing nuclear size and nuclear to cytoplasmic ratio, increased nucleus staining (hyperchromasia), more mitotic figures and increasing variation in size and shape of cells and nuclei, which is called pleomorphism.

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14
Q

Modified Bloom-Richardson Grading System

A
  • Tubele formation – normally turns into a loss of tubele
    • Nuclear polmorphism - loo at nuclear size
    • Mitotic figures

Increase protein expression to increase proliferation and growth

The term grade is used to indicate differentiation, high grade being poorly differentiated Modified Bloom Richardson grading for breast cancer 
1. Tubules 
2. Mitoses 
3. Nuclear pleomorphism G1, G2, G3
Higher grade = more severe cancer 
Survival of eprson depends on grade
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15
Q

Carcinoma in situ

A

• Carcinoma in situ = still limited by basement membrane and can’t invade tissue and dermis

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16
Q

Invasive carcinoma

A

• Invasive carcinoma = invade past basement membrane

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17
Q

Evolution of a squamous cell carcinoma

A
  1. Normal
    1. Dysplasia
    2. Carcinoma in situ – all cells have changed but basement membrane is still intact
    3. Invasion – erosion of basement membrane tumour accesses vascular channels
    4. Metastasi – can spread to different organs through blood or lymph
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18
Q

Stages in the development of a carcinoma

A
  • Normal tissue
    • Dysplasia and abnormalities
    • Full blow cancer cells invading underneath tissues
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19
Q

Carcinoma

A

Malignant tumour of epithelial cells

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20
Q

Characteristics of benign tumour

A
• Sessile 
	• Pedunculated 
	• Paillary 
These 3 are normally on benign tumours – don't invade, limited 
	• Exophilic growth grow outwards 
Surface in intact
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21
Q

Characteristics of malignant tumours

A
• Exophytic/ fungating 
	• Ulcerated
	• Annular 
These 3 are normally malignant tumours 
	• Invade tissue 
	• Endophytic growth 
	• Invade blood and lymph 
	• Look like a crab 
	•  Necrosis inside
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22
Q

Cancer cells must

A
• Sustaining proliferative signalling 
		○ Signalling is important – cells won't proliferate without signals 
	• Evading growth supressors 
		○ Avoid p53 
	• Ennabling replciative mortality 
		○ Find away to mainatin telomeres – telomerase 
	• Introducing angiogenesis 
	• Resisitng cell death 
		○ Resist apoptosis
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23
Q

Genetic Alterations:

A
  • Mutations,
    • deletions,
    • amplifications,
    • translocations,
    • rearrangements
24
Q

Epigenetic changes:

A
  • DNA methylation,

* chromatin modifications

25
Tumour supressor – in cancer
e.g. p53 or APC • Genes that control important pathways • Are mutated and destroyed
26
Oncogenes
* Normal genes that have been changed to cause uncontrolled growth * Are made more active though mutations * Loose repressive control of it so it is expressed a lot
27
Cancer cells aim to
Inhibit tumour suppressor | Activate oncogenes
28
Monoclonal
A collection of cells is monoclonal if they all originated from a single founding cell. • Tumours are monoclonal = start from one cell
29
Intratumoural Heterogeneity: non-clonal and clonal
---> same cells in one tumour can have different subclones with different genetic properties
30
Oma
• Benign neoplasms ends in –oma.
31
Sarcoma
–sarcoma if it is a stromal malignant neoplasm. Malignant tumour of connective tissue
32
Naming neoplasms
• Takes into account a neoplasm’s site of origin, whether it is benign or malignant, the type of tissue the tumour forms and sometimes the gross morphology (e.g. cyst or papilloma).
33
Carcinoma - features
``` • Epitehlieum origin • Malignant • Common • Lymph metastasis • In sity phase Usually over 50 years ```
34
Sarcoma - features
* Connective tisues (mesenchyme) * Malignant ]relatively rare * Blood metastasis * No in situ phase * Usually below 50 years
35
Epithelial neoplasms - benign
Papilloma | Adenomas
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Papilloma
Benign! • Squamous cell papilloma (any tumour with finger-like projections) – e.g. skin, buccal mucosa • Transitional cell papilloma – e.g. Bladder mucosa
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Adenoma
Benign! Glandular adenoma • Adenoma – e.g. adenomatous polyp of the colon Cystadenoma – e.g. ovary
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Epithelial neoplasms - malignant
' Carcinoma
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carcinoma - examples
• Squamous cell carcinoma: skin, larynx, oesophagus, lung, others • Transitional cell carcinoma: bladder, ureters • Adenocarcinoma: stomach, colon, lung, prostate, breast, pancreas, oesophagus, others Other Basal cell carcinoma: skin
40
Haematopoietic neoplasm
Malignant Haematopoietic = acute and chronic leukaemia • Occurs in bone marrow and abnormal cells then enter blood
41
Lymphoid neoplasm
Malignant Lymphoid = lymphoma (B and T) • Occurs in lymphoid tissue, usually in lymph nodes • Hodgkins & Non Hodgkins lymphomas
42
Myeloma
Malignant Myeloma (Multiple myeloma) • Occurs in the bone marrow plasma cells • Can affect several areas of the body
43
Testis - neoplasms
* Seminoma (malignant neoplasm) | * Non-seminomas (malignant teratoma)
44
Ovary - neoplasms
• Benign teratoma = dermoid cyst • Malignant germ cell ovarian tumours Can produce skin tissue, hair, teeth
45
Embryonal tumours: blastomas
``` Retinoblastoma: Rb – eye Nephroblastoma: Wilm’s tumour - kidney Neuroblastoma - kidney Medulloblastoma - cerebellum Hepatoblastoma – liver ```
46
Neuroendocrine tumours
Carcinoid tumours (various organs) Phaeochromocytoma (adrenal) Small cell carcinoma of bronchus
47
Hamartomas
• Benign • usually consist of two or more mature cell types normally found in the organ in which the lesion arises. E.g. adenochondroma: cartilage and bronchial-type epithelium • may be mistaken for malignant neoplasms on a chest X-ray • hamartomas are sometimes associated with clinical syndromes, e.g. in tuberous sclerosis
48
Cysts
* a fluid-filled space lined by epithelium * Some could be neoplastic, but many are not * neoplastic (e.g. cystadenoma, cystadenocarcinoma, cystic teratoma) * congenital (e.g. branchial and thyroglossal cysts due to embryological defects * parasitic (e.g. hydatid cysts due to Echinococcus granulosus) * retention (e.g. epidermoid and pilar cysts of the skin) * implantation (e.g. a result of surgical or accidental implantation of epidermis
49
Lobar pneumonia
* Neutrophils within an alveolus * Neutrophils within a blood vessel (red blood cells in lumen) – neutrophils are showing margination (blood fill begins to slow move closer to vessel wall) * Inflammatory exudate
50
Granuloma
* Granuloma outlined in red * Langhans type giant cell shown with black arrow = horeshow appearance nuclei in cell * Epitheliod histiocytes – activated macrophages Non caseating granuloma – no necrosis in the middle
51
Calcium soaps in acute pancreatitis
* Calcium soaps (white spots) on pancreas– lipases released from damaged pancreas * break down fatty tissue causing fat necrosis. * Released free fatty acids react with calcium to form chalky deposits (calcium soaps)
52
Fibrous adhesions in small intestines
* Fibrous bands forms between 2 parts of intestine after surgery – becoem connected * Cause complications
53
Struma ovarrii
Rare ovarian tumour defined by presence of thyroid tissue comprising more than half of the overall mass
54
Leukaemia
Haemopioetic malignant neoplasm of bone marrow
55
Lymphoma
Malignant neoplasm of lymphoid tissue
56
Polyp
Projecting growth of tissue from a surface in the body usually mucous membrane