Pre by lect : MR.ZAHID REHMAN
IPMS(KMU)
NEOPLASIA
Definition
Neoplasia means abnormal new growth.
Neo means new and plasia means growth.
Cellular proliferation and growth
Uncontrolled
R.A WILLIS (oncologist) define the neoplasia
Abnormal mass of tissue, the growth of which exceed
and is uncoordinated with that of the normal tissue
and persists in the same excessive manners after the
cessation of the stimuli which evoked the changes.
The study of neoplasm(tumor) is called oncology.
Difference between neoplasia and hyperplasia
Neoplasia hyperplasia
1.Not under normal control normal control
and it.s uncoordinated
2. Don’t stop when the source stop when the
source is
Is removed removed.
3.poor differentiated well differentiated
Nomenclature
Components of neoplasm:
Paranchyma:
It,s Contributes the proliferating part of the
neoplasm. Made of neoplastic cell.
Stroma.
It is made up of connective tissue, blood vessel and
lymphatics.
it provides support for the growth of paranchymal
cells.
Provide blood supply to neoplastic cell and also
give framework.
On the basis of clinical course
2 types of neoplasms
 Benign
 Malignant
Benign tumors
 Well differentiated
 low mitosis
 no necrosis
 Slow growing
 Well demarcated
 Encapsulated
 Do not infiltrate or metastasize
 May not recurrence
 Low dysplasia
Named with suffix –oma
Example:
benign tumor of epithelial origion.
Adenoma : adenoma is a benign tumor of epithelial
origion that resemble a glandular pattern or a
benign tumor of glandular origion that may not
resemble glandular structer.
It.s means any benign tumor derivates from the
glands. Or derivated from the epithelial tissue
that.s not glands but the tumor shows glandular
structer is called adenoma.
 Papillomas-
finger like projections raised from an epithelial
surface.
 Cyst adenoma
 Plyps
A polyp is an abnormal growth of tissue projecting fro
m a mucous membrane
 Polyps are commonly found in the colon,stomach, n
ose, urinary bladder and uterus
Benign tumor arise from the mesenchymal tissue :
 Smooth muscle-leiomyoma (fibroid)
 Benign tumor arising from fibroblast cells is called
fibroma.
 Benign tumor arise from menings is called
meningioma.
 Osteoma:
The benign tumor arise from bones.
 Chrondoma:
Benign tumor arise from the cartilage.
 Lipoma:
Benign tumor arises from fat of cells in
subcutanous tissue arises from cartilages.
Other term which are not a benign tumor bt
sound like a benign tumor
 Heamatoma
 Granuloma
 Choriostoma
Presence of normal tissue in normal ectopic
location. E.g presence of pancreas tissue in the
intestine.
Malignant tumors
Malignent tumor means cancer (crab)
 Well to poorly differentiated
 analplasia
 High mitosis
 Grow rapidly
 bleed
 Infiltrate
 metastasize
 Recur Metastasis
Cytologic features of malignant neoplasms include:
 Increased nuclear size (with increased
nuclear/cytoplasmic ratio--N/C ratio).
 Variation in nuclear or cell size (pleomorphism).
 Lack of differentiation (anaplasia).
 Increased nuclear DNA content with subsequent
dark staining (hyperchromatism).
 Prominent nucleoli or irregular chomatin
distribution within nuclei.
 Mitoses (especially irregular ).
 Spread of Malignant Neoplasms
 By direct extension (invasion) into surrounding
tissues.
 Through lymph channels to lymph nodes
(lymphatic spread)--typical of carcinomas.
 Via the bloodstream (hematogenous spread)--
typical of carcinomas or sarcomas.
 Within body cavities (seeding)--typical of
neoplasms impinging upon body cavities, such as
the peritoneal cavity.
Nomenclature
Types of malignent tumor:
Carcinoma:
The malignent tumor of epithelail cell origion are
called carcinoma. The word carcinoma is
attached to the epithelail tissue e.g. malignent
eipithelail tumor of renal cell is called renal cell
carcinoma.
Epithelial region
More common
Necrosis common
Hemorrhages less frequent
Example :
Adenocarcinoma :
The carcinoma in which neoplastic epithelial cells
grow in gland pattern is called adenocarcinoma.
Adenocarcinoma of renal cell , stomach , colon,
breast , gall bladder, prostate and uterus.
Squamous cell carcinoma :
The carcinoma in which neoplastic cells resemble
stratifeid squamous epitheluim is called
squamous cell carcinoma.the carcinoma arising
from the area either coverd by stratifeid
squamous epithelium(e.g skin, oral cavity,
esophagus)
Sarcoma :
The malignent tumor arsing in mesenchymal tissue
are called sarcoma. e.g malignent tumor of
fibroblastic cells is called fibrosarcoma.
Mesenchyamal origion
Less common
Necrosis less common
Hemorrhages more frequent.
Example
 Fibrosarcoma :
This tumor arises most commonly from facia ,
intermuscular and subcutaneuos tissue.
 Chondrosarcoma
 Osteogenic sarcomas
 Leiomysarcoma
 Liposarcoma.
renal cell carcinoma
Hepatocellular carcinoma
renal cell
carcinoma
Malignent tumor of lungs Ductal carcinoma of breast
osteosarcoma
The sarcoma seen at medium magnification is
composed of pleomorphic cells that vary
markedly in size and shape. The increased
amounts of nuclear DNA, making them
hyperchromatic. The cell of origin of sarcomas is
often difficult to determine because of their
tendency to be poorly differentiated or even
anaplastic.
This sarcoma has many mitoses. A very
large abnormal mitotic figure is seen.
Principle of tumor
1. Non lethal mutation
2. Monoclonolity
3. Protooncogenesis
4. Tumor supressor gene
5. Gene regualating appoptosis
6. Gene regulating DNA repair
1. Non lethal mutation:
Non lethal mutation is a type of mutation in which
there is permanent hereditory changes in the
DNA base sequence however the cell did,nt die.
If the mutation was lethal , the cell would be die , if
the cell deid so there is no way to cancer
developed.
Non lethal mutation result in carcinogenesis when
the mutation will alter protooncogenesis and
tumor supressor gene can result caner
formation.
Gene :
Gene is a unit of DNA , that encoted a particular
protein or RNA molecules or unit of hereditory.
Mutation alter the gene.
Mutation :
Permanent , hereditable changes in the base
sequence of DNA of an organ. Mutation due to
radiation, toxidity etc.
Monoclonality :
Most of the tumor are monoclonol .
The tumor is formed from the clonol expansion of
the single precurssor cell that had encounterd in
non lethal mutation.
4 target gene for genetic damage
Protooncogenesis :
Nomal gene that is found in our cell it.s function is
to encote protein that regulate the cell
proliferation and cell differentiation and it has
some role in signal transdiction, also role in
mitosis and cell cycle.
We need the protooncogenesis for the normal
growth and differentiation of cell. When these
protooncogenesis get mutated so its called
oncogenesis.
Oncogenesis can result cancer developed .
 in non-mutant state called
 proto-oncogenes
 stimulate cell growth and replication
 when turned “on” by mutation cause
uncontrolled growth called
oncogeneses.
Tumor supressor gene :
Opposite to oncogene.
 Inhibit cell proliferate and also inhibit tumor
development.
 negatively regulate proliferation -
antioncogenes
 want these to remain intact
 takes two “hits” to remove both genes
Gene regulating apoptosis :
Apoptosis is a pathway of programe cell death.
Apoptosis is a better alternative when the cell is so
much damaged so then DNA can,t be repair so
there will be a risk of mutation of DNA result in
cancer.
Cause are rediation , some viral infection.
Gene regulating DNA repair :
Target of genetic damaged .
If there is damaged in these gene that will also
result cancer formation indirectly . If the gene
damaged it will decrease the regulate the DNA
repair.
Protooncogenesis and tumor supressor gene when
these
gene getting damaged , lack of repair it will
developed the formation of cancer.
 Genetics and cancer prone families
 to be passed down, mutations must occur in
germ cells
 inherited mutations almost always in tumor
suppressor genes
 Epstein-Barr and Kaposi sarcoma
 both herpes viruses
 Human T cell leukemia-lymphoma virus
 blood transfusions, needles, sex and
breast feeding
 Bacterial causes of Cancer
 Helicobacter pylori infects >1/2 world’s
population
 assoc. with B cell lymphomas of the
Environmental factors
 Tobacco use
 Diet
 Alcohol use
 Sexual and reproductive behavior
 Air pollution
 UV radiation and other radiation
 hormones
Metastasis
Tumor implants discontinue from the primary tumor
is called metastasis.
Spread:
 Spread by lymphatic system
 Hematogenous routs
 Seeding of body cavities
 Malignant neoplasms are capable of
metastasizing. A metastasis represents a
malignant neoplasm that has traveled from its
primary site of origin to a distant site. This is an
example of metastases to the liver.
 A primary neoplasm is more likely to appear
within an organ as a solitary mass. The presence
of metastases is an indication that a neoplasm is
malignant.
The original clone of cells that developed into a
neoplasm may not have had the ability to
metastasize, but continued proliferation of the
neoplastic cells and acquisition of more genetic
mutations within the neoplastic cells can give
them the ability to metastasize.
Seeding of body cavities and surface
This occure when a malignent neoplasim penetrate
into a natural “open field” such as peritoneal
cavity , pleural space, pericardial cavity etc.
Example :
 Ovarian carcinoma
 Appendicle carcinoma
Neoplasms can spread by seeding within body
cavities such as the pleural cavity or peritoneal
cavity. This pattern of spread is more typical for
carcinomas than other neoplasms. Note the
multitude of small tan tumor nodules seen over
the peritoneal surface of the mesentery shown
here.
Lymphatic spread
Most common pathway for dissemination or
spreading of carcinoma ( sarcoma also use this
routs) . The pattern of lymphnode involment
follows the natural routs of drainage.
Hematogenous spread
This pathway is typical of sarcoma . Due to
elasticity arteries are more difficult for tumor to
penetrate then vein. With the venous invasion the
tumor cell follow the venous flow drainage.
Common metastatic sites
Liver
Lung
Bone
Brain
Adrenal; Lung and breast
Gastric carcinoma
Krukenberg tumor: Gastric met to ovary
Staging
 Staging is a way of describing how much a
cancer has grown and spread. A common way of
staging cancer is called the TNM classification:
 T stands for tumour - how far the primary tumour
has grown locally.
 N stands for nodes - if the cancer has spread to
the local lymph glands (nodes).
 M stands for metastases - if the cancer has
spread to other parts of the body.
 Example:
 in stomach cancer:
 T-1 means the primary tumour is still in the stomach
wall. T-3 means the primary tumour has grown right
through the stomach wall and T-4 means it is invading
nearby structures such as the pancreas.
 N-0 means there is no spread to lymph nodes. N-1
means that some local lymph nodes are affected. N-2
means more extensive spread to local lymph nodes.
 M-0 means there are no metastases. M-1 means that
there are metastases to some other area of the body
such as the liver or brain.
Grading
 Some cancers are also graded. A sample of the
cancer (a biopsy) is looked at under the microscope
or tested in other ways. By looking at certain features
of the cells, the cancer can be graded as low,
intermediate or high.
 Low-grade means the cancer cells tend to be slow-
growing, look quite similar to normal cells (are well
differentiated), tend to be less aggressive, and are
less likely to spread quickly.
 Intermediate-grade is a middle grade.
 High-grade means the cancer cells tend to be fast
growing, look very abnormal (are poorly
differentiated), tend to be more aggressive, and are
more likely to spread quickly.
THANK YOU

01 NEOPLASIA.pptx

  • 1.
    Pre by lect: MR.ZAHID REHMAN IPMS(KMU) NEOPLASIA
  • 2.
    Definition Neoplasia means abnormalnew growth. Neo means new and plasia means growth. Cellular proliferation and growth Uncontrolled R.A WILLIS (oncologist) define the neoplasia Abnormal mass of tissue, the growth of which exceed and is uncoordinated with that of the normal tissue and persists in the same excessive manners after the cessation of the stimuli which evoked the changes. The study of neoplasm(tumor) is called oncology.
  • 3.
    Difference between neoplasiaand hyperplasia Neoplasia hyperplasia 1.Not under normal control normal control and it.s uncoordinated 2. Don’t stop when the source stop when the source is Is removed removed. 3.poor differentiated well differentiated
  • 4.
    Nomenclature Components of neoplasm: Paranchyma: It,sContributes the proliferating part of the neoplasm. Made of neoplastic cell. Stroma. It is made up of connective tissue, blood vessel and lymphatics. it provides support for the growth of paranchymal cells. Provide blood supply to neoplastic cell and also give framework.
  • 5.
    On the basisof clinical course 2 types of neoplasms  Benign  Malignant Benign tumors  Well differentiated  low mitosis  no necrosis  Slow growing  Well demarcated
  • 6.
     Encapsulated  Donot infiltrate or metastasize  May not recurrence  Low dysplasia
  • 7.
    Named with suffix–oma Example: benign tumor of epithelial origion. Adenoma : adenoma is a benign tumor of epithelial origion that resemble a glandular pattern or a benign tumor of glandular origion that may not resemble glandular structer. It.s means any benign tumor derivates from the glands. Or derivated from the epithelial tissue that.s not glands but the tumor shows glandular structer is called adenoma.
  • 8.
     Papillomas- finger likeprojections raised from an epithelial surface.  Cyst adenoma  Plyps A polyp is an abnormal growth of tissue projecting fro m a mucous membrane  Polyps are commonly found in the colon,stomach, n ose, urinary bladder and uterus Benign tumor arise from the mesenchymal tissue :  Smooth muscle-leiomyoma (fibroid)  Benign tumor arising from fibroblast cells is called fibroma.  Benign tumor arise from menings is called meningioma.
  • 9.
     Osteoma: The benigntumor arise from bones.  Chrondoma: Benign tumor arise from the cartilage.  Lipoma: Benign tumor arises from fat of cells in subcutanous tissue arises from cartilages.
  • 10.
    Other term whichare not a benign tumor bt sound like a benign tumor  Heamatoma  Granuloma  Choriostoma Presence of normal tissue in normal ectopic location. E.g presence of pancreas tissue in the intestine.
  • 14.
    Malignant tumors Malignent tumormeans cancer (crab)  Well to poorly differentiated  analplasia  High mitosis  Grow rapidly  bleed  Infiltrate  metastasize  Recur Metastasis
  • 15.
    Cytologic features ofmalignant neoplasms include:  Increased nuclear size (with increased nuclear/cytoplasmic ratio--N/C ratio).  Variation in nuclear or cell size (pleomorphism).  Lack of differentiation (anaplasia).  Increased nuclear DNA content with subsequent dark staining (hyperchromatism).  Prominent nucleoli or irregular chomatin distribution within nuclei.  Mitoses (especially irregular ).
  • 16.
     Spread ofMalignant Neoplasms  By direct extension (invasion) into surrounding tissues.  Through lymph channels to lymph nodes (lymphatic spread)--typical of carcinomas.  Via the bloodstream (hematogenous spread)-- typical of carcinomas or sarcomas.  Within body cavities (seeding)--typical of neoplasms impinging upon body cavities, such as the peritoneal cavity.
  • 17.
    Nomenclature Types of malignenttumor: Carcinoma: The malignent tumor of epithelail cell origion are called carcinoma. The word carcinoma is attached to the epithelail tissue e.g. malignent eipithelail tumor of renal cell is called renal cell carcinoma. Epithelial region More common Necrosis common Hemorrhages less frequent
  • 18.
    Example : Adenocarcinoma : Thecarcinoma in which neoplastic epithelial cells grow in gland pattern is called adenocarcinoma. Adenocarcinoma of renal cell , stomach , colon, breast , gall bladder, prostate and uterus. Squamous cell carcinoma : The carcinoma in which neoplastic cells resemble stratifeid squamous epitheluim is called squamous cell carcinoma.the carcinoma arising from the area either coverd by stratifeid squamous epithelium(e.g skin, oral cavity, esophagus)
  • 19.
    Sarcoma : The malignenttumor arsing in mesenchymal tissue are called sarcoma. e.g malignent tumor of fibroblastic cells is called fibrosarcoma. Mesenchyamal origion Less common Necrosis less common Hemorrhages more frequent.
  • 20.
    Example  Fibrosarcoma : Thistumor arises most commonly from facia , intermuscular and subcutaneuos tissue.  Chondrosarcoma  Osteogenic sarcomas  Leiomysarcoma  Liposarcoma.
  • 21.
    renal cell carcinoma Hepatocellularcarcinoma renal cell carcinoma
  • 22.
    Malignent tumor oflungs Ductal carcinoma of breast
  • 23.
  • 24.
    The sarcoma seenat medium magnification is composed of pleomorphic cells that vary markedly in size and shape. The increased amounts of nuclear DNA, making them hyperchromatic. The cell of origin of sarcomas is often difficult to determine because of their tendency to be poorly differentiated or even anaplastic. This sarcoma has many mitoses. A very large abnormal mitotic figure is seen.
  • 25.
    Principle of tumor 1.Non lethal mutation 2. Monoclonolity 3. Protooncogenesis 4. Tumor supressor gene 5. Gene regualating appoptosis 6. Gene regulating DNA repair
  • 26.
    1. Non lethalmutation: Non lethal mutation is a type of mutation in which there is permanent hereditory changes in the DNA base sequence however the cell did,nt die. If the mutation was lethal , the cell would be die , if the cell deid so there is no way to cancer developed. Non lethal mutation result in carcinogenesis when the mutation will alter protooncogenesis and tumor supressor gene can result caner formation.
  • 27.
    Gene : Gene isa unit of DNA , that encoted a particular protein or RNA molecules or unit of hereditory. Mutation alter the gene. Mutation : Permanent , hereditable changes in the base sequence of DNA of an organ. Mutation due to radiation, toxidity etc.
  • 28.
    Monoclonality : Most ofthe tumor are monoclonol . The tumor is formed from the clonol expansion of the single precurssor cell that had encounterd in non lethal mutation.
  • 29.
    4 target genefor genetic damage Protooncogenesis : Nomal gene that is found in our cell it.s function is to encote protein that regulate the cell proliferation and cell differentiation and it has some role in signal transdiction, also role in mitosis and cell cycle. We need the protooncogenesis for the normal growth and differentiation of cell. When these protooncogenesis get mutated so its called oncogenesis. Oncogenesis can result cancer developed .
  • 30.
     in non-mutantstate called  proto-oncogenes  stimulate cell growth and replication  when turned “on” by mutation cause uncontrolled growth called oncogeneses.
  • 31.
    Tumor supressor gene: Opposite to oncogene.  Inhibit cell proliferate and also inhibit tumor development.  negatively regulate proliferation - antioncogenes  want these to remain intact  takes two “hits” to remove both genes
  • 32.
    Gene regulating apoptosis: Apoptosis is a pathway of programe cell death. Apoptosis is a better alternative when the cell is so much damaged so then DNA can,t be repair so there will be a risk of mutation of DNA result in cancer. Cause are rediation , some viral infection.
  • 33.
    Gene regulating DNArepair : Target of genetic damaged . If there is damaged in these gene that will also result cancer formation indirectly . If the gene damaged it will decrease the regulate the DNA repair. Protooncogenesis and tumor supressor gene when these gene getting damaged , lack of repair it will developed the formation of cancer.
  • 34.
     Genetics andcancer prone families  to be passed down, mutations must occur in germ cells  inherited mutations almost always in tumor suppressor genes
  • 35.
     Epstein-Barr andKaposi sarcoma  both herpes viruses  Human T cell leukemia-lymphoma virus  blood transfusions, needles, sex and breast feeding  Bacterial causes of Cancer  Helicobacter pylori infects >1/2 world’s population  assoc. with B cell lymphomas of the
  • 36.
    Environmental factors  Tobaccouse  Diet  Alcohol use  Sexual and reproductive behavior  Air pollution  UV radiation and other radiation  hormones
  • 37.
    Metastasis Tumor implants discontinuefrom the primary tumor is called metastasis. Spread:  Spread by lymphatic system  Hematogenous routs  Seeding of body cavities
  • 38.
     Malignant neoplasmsare capable of metastasizing. A metastasis represents a malignant neoplasm that has traveled from its primary site of origin to a distant site. This is an example of metastases to the liver.  A primary neoplasm is more likely to appear within an organ as a solitary mass. The presence of metastases is an indication that a neoplasm is malignant.
  • 39.
    The original cloneof cells that developed into a neoplasm may not have had the ability to metastasize, but continued proliferation of the neoplastic cells and acquisition of more genetic mutations within the neoplastic cells can give them the ability to metastasize.
  • 40.
    Seeding of bodycavities and surface This occure when a malignent neoplasim penetrate into a natural “open field” such as peritoneal cavity , pleural space, pericardial cavity etc. Example :  Ovarian carcinoma  Appendicle carcinoma
  • 41.
    Neoplasms can spreadby seeding within body cavities such as the pleural cavity or peritoneal cavity. This pattern of spread is more typical for carcinomas than other neoplasms. Note the multitude of small tan tumor nodules seen over the peritoneal surface of the mesentery shown here.
  • 42.
    Lymphatic spread Most commonpathway for dissemination or spreading of carcinoma ( sarcoma also use this routs) . The pattern of lymphnode involment follows the natural routs of drainage. Hematogenous spread This pathway is typical of sarcoma . Due to elasticity arteries are more difficult for tumor to penetrate then vein. With the venous invasion the tumor cell follow the venous flow drainage.
  • 43.
    Common metastatic sites Liver Lung Bone Brain Adrenal;Lung and breast Gastric carcinoma Krukenberg tumor: Gastric met to ovary
  • 44.
    Staging  Staging isa way of describing how much a cancer has grown and spread. A common way of staging cancer is called the TNM classification:  T stands for tumour - how far the primary tumour has grown locally.  N stands for nodes - if the cancer has spread to the local lymph glands (nodes).  M stands for metastases - if the cancer has spread to other parts of the body.
  • 45.
     Example:  instomach cancer:  T-1 means the primary tumour is still in the stomach wall. T-3 means the primary tumour has grown right through the stomach wall and T-4 means it is invading nearby structures such as the pancreas.  N-0 means there is no spread to lymph nodes. N-1 means that some local lymph nodes are affected. N-2 means more extensive spread to local lymph nodes.  M-0 means there are no metastases. M-1 means that there are metastases to some other area of the body such as the liver or brain.
  • 46.
    Grading  Some cancersare also graded. A sample of the cancer (a biopsy) is looked at under the microscope or tested in other ways. By looking at certain features of the cells, the cancer can be graded as low, intermediate or high.  Low-grade means the cancer cells tend to be slow- growing, look quite similar to normal cells (are well differentiated), tend to be less aggressive, and are less likely to spread quickly.  Intermediate-grade is a middle grade.  High-grade means the cancer cells tend to be fast growing, look very abnormal (are poorly differentiated), tend to be more aggressive, and are more likely to spread quickly.
  • 47.