Tumour typing grading and staging
What these are mean and what the benefits from its
Typing, grading and staging are important for
Planning of treatment
Type and degree of surgical excision
Consideration of pre-operative radiotherapy or chemotherapy to downsize
To provide accurate prognostic information
For the patient
For the physician
To provide accurate comparison between outcome in different patient
Comparisons between treatments
Comparisons between centres
Comparison of features in benign vs malignant
Benign neoplasms
• Expansile, usually slow growing
• Don not metastasise
• Low mitotic rate, little pleomorphism
• Normal chromosome numbers
• Necrosis and haemorrhage unusual
• More likely to be polypoid or papillary NB not all
Malignant neoplasms
• Infiltrative, irregular or fast growth rate
• May metastasise
• Pleomorphic, frequent mitotic figures
• Abnormal chromosome numbers
• Necrosis and haemorrhage may occur
• May be fungating or ulcerated
Tumour typing
the first piece of relevant information is the type of tumour. Tumours may be identified by similarity of their cells to the tissue of origin, if they remain well differentiated. With a poorly
differentiated metastatic deposit it may be impossible to identify its source. neoplasm are named according to whether they arise from epithelium or stroma
Epithelial neoplasms as .Adenoma: benign epithelial neoplasm forming a glandular pattern or arising from a gland.but not necessarily forming a glandular pattern
Papilloma: benign epithelial neoplasm protruding from a surface which produces
finger-like fronds made up of connective tissue processes covered by epithelial cells
.Cystadenoma: benign epithelial neoplasm arising from duct or gland epithelium with secrtion and distension of the lumen due to lack of drainage
-Carcinoma: a malignant epithelial neoplasm
mesnechymal neoplasms
these are named according to cell type
oma: if benign eg lipoma
sarcoma: if malignant eg osteosarcoma
Tumour grading
This is an assessment of the degree of differentiation of a tumour and corresponds to the
aggressive behaviour of the tumour. Tumours are graded as
• Well differentiated
• Moderately differentiated
• Poorly/undifferentiated/anaplastic
Many different grading systems exist for different tumours that take into consideration growth patterns as well as differentiation status eg Gleason grade for prostate cancer
Differentiation refers to the degree to which neoplastic cells resemble their tissue of origin
Features of poor differentiation are
• Increased nuclear pleomorphism
• Atypical mitoses
• Hyperchromatic nuclei
• Increased nuclear to cytoplasmic size ratio
• Giant cells may be present
Tumour grading is important for prediction of tumour behaviour and prognosis. In general the less differentiated the tumour, the more aggressive its biological behaviour
Tumour staging
This refers to the size and spread of the neoplasm as assessed by clinician, pathologist or sed for decisions on management and prognosis
Examples for tumour staging
Dukes' classification for colorectal carcinoma
Clark's classification for malignant melanoma
TNM tumour, node metastasis system
staging often requires extensive investigations of the sites most likely to be involved in disease and is aimed at assessing degree of tumour spread to regional nodes and distant site
.Blood tests eg LFTs, tumour markers
Cytology or biopsy for histology
Chest X-ray or CT
Abdominalinal USS or CT
MRI isotope bone scanning
Position emission topography PET
Diagnostic or staging laparoscopy
Full staging may not be possible until after surgery to resect the tumour when regional lymph nodes can be inspected histologically for tumour deposits
failure to identify distant metastasis at the time of staging does not necessarily
mean that the patient is free from all tumour cells after resection of the primary. tumour cells continue to be present in the circulation until the primary is removed there may be tiny, as yet undetectable, metastatic deposits in other organs or lymph nods
TNM classification
The TMN classification was first developed by the American Joint Committee on Cancer
staging and Result Reporting and has now been modified for systems for most solid breast, colon, thyroid.
The TNM staging system
Cytology or biopsy for histology
Chest X-ray or CT
Abdominalinal USS or CT
MRI isotope bone scanning
Position emission topography PET
Diagnostic or staging laparoscopy
Full staging may not be possible until after surgery to resect the tumour when regional lymph nodes can be inspected histologically for tumour deposits
failure to identify distant metastasis at the time of staging does not necessarily
mean that the patient is free from all tumour cells after resection of the primary. tumour cells continue to be present in the circulation until the primary is removed there may be tiny, as yet undetectable, metastatic deposits in other organs or lymph nods
TNM classification
The TMN classification was first developed by the American Joint Committee on Cancer
staging and Result Reporting and has now been modified for systems for most solid breast, colon, thyroid.
The TNM staging system
T = primary tumour
.To = no primary tumour
Tis= in situ primary tumour
Tx = unknown primary tumour T1-4 Sizes of primary tumour
N = nodal metastasis
No No nodes
N1 Few node or nodes
N2-3 Relates to number, fixity, or distant lymph node group involvement
M = distant metastasis
Mo No metastasis
M1 Distant metastasis present
tags:tumour,grading,staging,typing
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