Neoplasia and Lung Cancer Flashcards
Distinguish the features of benign and malignant tumours - 4 key differences
1.) Degree of differentiation: How closely do the cell resemble a mature cell? The more differentiated the slower the rate of growth. Well differentiated = closely resemble tissue of origin. Extend determines how easily the location of the primary tumour can be identified.
2.) Rate of growth: > rate of growth = > accumulation of mutations = more difficult to treat
3.) Local Invasion
4.) Metastasis
Benign neoplasms (tumours)
Much better prognosis. Can be removed. Well differentiated, morphologically and functionally, closely resemble the origin tissue. Few mitoses. Grow slowly generally but can grow quickly under hormonal influence.
Malignant neoplasms (tumours)
Cancerous. Spread throughout the body - invade local tissues and then migrate to distant sites. The only type of tumour able to invade and metastasise. Generally grow quickly. Can be well differentiated or undifferentiated (anaplasm). This is due to dedifferentiation of mature cells or growth of stem cells. % of malignant cells = Tumour cellularity
Describe tumour differentiation
The process by which immature cells become mature cells with specialised functions. Well-differentiated tumours closely resemble their origin tissue. Also, normal cell receptors are present. They tend to grow at a slower rate.
Describe tumour invasion
Benign rarely invasive, often delineated by a fibrous capsule from host response and tumour. Malignant invade into blood vessels and local tissues. This is achieved by breaching the basement membrane. These pre-invasive tumours may be called intraepithelial neoplasm. Sees the breakdown of intercellular junctions (E-cadherin) –> BM and ECM degraded –> Attachment to novel ECM components –> Migration
Describe tumour angiogenesis
Excessive growth of neoplastic cells will cause development of a necrotic core, due to ischaemia. Necrotic cells in the centre of the tumour evoke inflammation which stimulate angiogenesis - creates nutrient supply for the tumour. Tumour cells and cells within the microenvironment also secrete factors to stimulate angiogenesis e.g. VEGF Antiangiogenic factors e.g. thalidomide
Describe tumour metastasis
Benign tumours compress adjacent tissues or release hormones, they cannot metastasise. Malignant tumours invade local tissues and then travel via the bloodstream or lymphatic system to new tissues. Tend to migrate to highly vascularised areas, such as the lungs, brain, adrenal glands, liver and bone.
Describe tumour progression
Initially the tumour is formed from a group of monoclonal cells. As division occurs and mutations arise a heterogeneous group of cells develops. Different divisions of cell are seen. Tumours change throughout growth. Personalised medicine aims to create the most suitable treatment as each tumour is so individual.
Describe tumour grading
Grade is found using a microscope, usually via a biopsy. Involves looking at the cells, looking at the number of cells (mitotic index), look how differentiated and pleomorphic they are, perform immune labelling. Allows the characteristics of the cells to be defined.
Describe tumour staging
Staging is decided using a scan. The TNM system is used: Tumour: Size, local invasion Nodes: Local of distal node involvement Metastasis: Can any be detected? A score in generated which helps direct treatment.
Understand the terminology relating to neoplasm
Neoplasm: New and permanent alteration of cell growth which persists upon removal of the stimulus.
Nomenclature: Benign epithelial neoplasms
~oma e.g. adenoma, papilloma Prefixed with tissue of origin e.g. renal adenoma
Nomenclature: Malignant epithelial neoplasms
Carcinoma, prefixed with cell type e.g. adenocarcinoma
Nomenclature: Benign parenchymal neoplasms (CN/muscle)
~oma e.g. chondroma, fibroma, lipoma, leiomyoma, rhabdomyoma, osteoma
Nomenclature: Malignant parenchymal neoplasms (CN/muscle
~sarcoma e.g. osteosarcoma