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By: Nityanand Upadhyay
Associate Professor
Department of MLT
Integral University, Lucknow
 The term ‘neoplasia’ means new growth.
 The new growth produced is called
‘neoplasm’ or ‘tumour’.
 However, all ‘new growths’ are not
neoplasms.
 examples of new growth of tissues and cells:
processes of embryogenesis, regeneration and
repair, hyperplasia and hormonal stimulation.
 The proliferation and maturation of cells in
normal adults is controlled, Coordinated and
having purpose.
 While neoplastic cells lose control and
regulation of replication and form an
abnormal mass of tissue.
Neoplasm or Tumour is
“Mass of tissue formed as a result
of abnormal, excessive,
uncoordinated, autonomous and
purposeless proliferation of cells
even after cessation of stimulus for
growth which caused it”
 The branch of science dealing with the study
of neoplasms or tumours is called oncology.
 (oncos=tumour, logos=study).
 The word ‘cancer’ means crab
 Hippocrates (460-377 BC) coined the term
karkinos for cancer of the breast.
 1. Benign: When they are slow-growing
and localised without causing much difficulty
to the host.
 2. Malignant: When they proliferate rapidly,
spread throughout the body and may
eventually cause death of the host.
 All tumours, benign as well as malignant,
have 2 basic components:
1. Parenchyma’ comprised by proliferating
tumour cells.
2. ‘Supportive stroma’ composed of fibrous
connective tissue and blood vessels.
1. Mixed tumours: When two types of tumours
are combined in the same tumour.
2. Teratomas:
3. Blastomas (Embryomas):
4. Hamartoma:
5. Choristoma:
 Classification of tumours is
based on the histogenesis.
 i.e. cell of origin
 Usually on basis of cell/tissue
of origin Main groups are:
 •Epithelial
 •Connective tissue
(mesenchymal)
 •Lymphoid/haematological
 •Mixture of all (teratomas)
Nomenclature
Tissue of origin
Epithelial:
Cell of origin Benign Malignant
•Squamous cell Papilloma Sq C carcinoma
•Glandular Adenoma Adenocarcinoma
•Transitional TC Papilloma T C carcinoma
•Basal Cell BC Papilloma B C carcinoma
Non-epithelial (Mesenchymal) Tumour :
Cell of origin Benign Malignant
. Adipose tissue Lipoma Liposarcoma
. Adult fibrous Fibroma Fibrosarcoma
tissue
. Embryonic Myxoma Myxosarcoma
Fibrous tissue
. Cartilage Chondroma Chondrosarcoma
Cell of origin Benign Malignant
. Bone Osteoma Osteosarcoma
. Smooth muscle Leiomyoma Leiomyosarcoma
. Skeletal muscle Rhabdomyoma Rhabdomyosarcom
. Mesothelium — Mesothelioma
. Blood vessels Haemangioma Angiosarcoma
. Lymphoid tissue Pseudolymphoma Malignant
lymphomas
MIXED TUMOURS:
Cell of origin Benign Malignant
. Salivary Pleomorphic - Malignant -
Glands adenoma mixed salivary -
tumour
TUMOURS OF MORE THAN ONE GERM CELL
LAYER:
.Totipotent cells Mature Immature
in gonads or teratoma teratoma
in embryonal rests
 I. Rate of growth
 II. Cancer phenotype and stem cells
 III. Clinical and gross features
 IV. Microscopic features
 V. Local invasion (Direct spread)
 VI. Metastasis (Distant spread).
Feature Benign Malignant
I. CLINICAL AND GROSS FEATURES:
1. Boundaries Encapsulated Irregular
2. Surrounding compressed Invaded
3. Size Small Larger
4. Secondary less often more often
changes
Feature Benign Malignant
II. MICROSCOPIC FEATURES:
1. Pattern : Resembles Poorly-
Resemblance
2. Pleomorphism: Not present Present
3. N:C ratio Normal Increase
4. Anisonucleosis Absent Present
Feature Benign Malignant
III. GROWTH RATE: Slow Rapid
IV. LOCAL INVASION:
 Benign: Often compresses the surrounding
tissues without invading or infiltrating them
 Malignant: Usually infiltrates and invades the
adjacent tissues.
Feature Benign Malignant
V. METASTASIS: Absent Present
VI. PROGNOSIS:
Benign: Local complications.
Malignant: Death by local and metastatic
complications.
 Grade I: Well-differentiated (less than 25%
anaplastic cells).
 Grade II: Moderately-differentiated (25-50%
anaplastic cells).
 Grade III: Moderately-differentiated (50-75%
anaplastic cells).
 Grade IV: Poorly-differentiated or anaplastic
(more than 75% anaplastic cells).
Men Women Children
1. Lung Breast Acute leukaemia
(oral cavity- (cervix in India)
in India)
2. Prostate Lung CNS tumour
3. Colorectal Colorectal Bone sarcoma
4. Urinary Endometrial Endocrine
bladder
 5. Lymphoma Lymphoma Soft tissue sarcoma
1. FAMILIAL AND GENETIC FACTORS.
. Multiple endocrine neoplasia (MEN).
. Neurofibromatosis
. Cancer of the breast: Female relatives of breast
cancer patients have 2 to 6 times higher risk of
developing breast cancer.
.
2. RACIAL AND GEOGRAPHIC FACTORS.
i) White Europeans and Americans develop
most commonly malignancies of the lung, breast,
and colon.
ii) Black Africans, on the other hand, have more
commonly cancers of the skin, penis, cervix and
liver.
iii) Japanese have five times higher incidence of
carcinoma of the stomach than the Americans.
3. ENVIRONMENTAL AND CULTURAL FACTORS.
i) Cigarette smoking : cancer of the oral cavity,
pharynx, larynx, oesophagus, lungs, pancreas
and urinary bladder.
ii) Alcohol: cancer of oropharynx, larynx,
oesophagus and liver.
iii) Alcohol and tobacco: cancer of the upper
aerodigestive tract.
iv) Paan in a particular place in mouth for a long
time.
vii) A large number of industrial and environmental
substances are carcinogenic: like arsenic,
asbestos, benzene, vinyl chloride, naphthylamine
etc.
iii) Certain constituents of diet: Overweight
individuals, deficiency of vitamin A and people
consuming diet rich in animal fats and low in
fibre content.
IV Pathogens:
Human papillomavirus (HPV),
EBV or Epstein-Barr virus,
hepatitis viruses B and C,
Kaposi's sarcoma-associated herpes virus
(KSHV), Merkel cell polyomavirus,
Schistosoma spp.,
and Helicobacter pylori; other bacteria are
being researched as possible agents.
 Fatigue
 Lump or area of thickening that can be felt under
the skin
 Weight changes, including unintended loss or gain
 Skin changes, such as yellowing, darkening or
redness of the skin, sores that won't heal, or
changes to existing moles
 Changes in bowel or bladder habits
 Persistent cough or trouble breathing
 Difficulty swallowing
 Hoarseness
 Persistent indigestion or discomfort after eating
 Persistent, unexplained muscle or joint pain
 Persistent, unexplained fevers or night sweats
 Unexplained bleeding or bruising
 Histopathological
 Cytopathological
 Haematological
 Tumour Marker
 Immunohistochemistry(IHC)
 Radiological : CT, MRI, PET CT.
Thanks…………..

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Neoplasia

  • 1. By: Nityanand Upadhyay Associate Professor Department of MLT Integral University, Lucknow
  • 2.  The term ‘neoplasia’ means new growth.  The new growth produced is called ‘neoplasm’ or ‘tumour’.  However, all ‘new growths’ are not neoplasms.  examples of new growth of tissues and cells: processes of embryogenesis, regeneration and repair, hyperplasia and hormonal stimulation.
  • 3.  The proliferation and maturation of cells in normal adults is controlled, Coordinated and having purpose.  While neoplastic cells lose control and regulation of replication and form an abnormal mass of tissue.
  • 4. Neoplasm or Tumour is “Mass of tissue formed as a result of abnormal, excessive, uncoordinated, autonomous and purposeless proliferation of cells even after cessation of stimulus for growth which caused it”
  • 5.  The branch of science dealing with the study of neoplasms or tumours is called oncology.  (oncos=tumour, logos=study).  The word ‘cancer’ means crab  Hippocrates (460-377 BC) coined the term karkinos for cancer of the breast.
  • 6.  1. Benign: When they are slow-growing and localised without causing much difficulty to the host.  2. Malignant: When they proliferate rapidly, spread throughout the body and may eventually cause death of the host.
  • 7.  All tumours, benign as well as malignant, have 2 basic components: 1. Parenchyma’ comprised by proliferating tumour cells. 2. ‘Supportive stroma’ composed of fibrous connective tissue and blood vessels.
  • 8. 1. Mixed tumours: When two types of tumours are combined in the same tumour. 2. Teratomas: 3. Blastomas (Embryomas): 4. Hamartoma: 5. Choristoma:
  • 9.  Classification of tumours is based on the histogenesis.  i.e. cell of origin
  • 10.  Usually on basis of cell/tissue of origin Main groups are:  •Epithelial  •Connective tissue (mesenchymal)  •Lymphoid/haematological  •Mixture of all (teratomas)
  • 11. Nomenclature Tissue of origin Epithelial: Cell of origin Benign Malignant •Squamous cell Papilloma Sq C carcinoma •Glandular Adenoma Adenocarcinoma •Transitional TC Papilloma T C carcinoma •Basal Cell BC Papilloma B C carcinoma
  • 12. Non-epithelial (Mesenchymal) Tumour : Cell of origin Benign Malignant . Adipose tissue Lipoma Liposarcoma . Adult fibrous Fibroma Fibrosarcoma tissue . Embryonic Myxoma Myxosarcoma Fibrous tissue . Cartilage Chondroma Chondrosarcoma
  • 13. Cell of origin Benign Malignant . Bone Osteoma Osteosarcoma . Smooth muscle Leiomyoma Leiomyosarcoma . Skeletal muscle Rhabdomyoma Rhabdomyosarcom . Mesothelium — Mesothelioma . Blood vessels Haemangioma Angiosarcoma . Lymphoid tissue Pseudolymphoma Malignant lymphomas
  • 14. MIXED TUMOURS: Cell of origin Benign Malignant . Salivary Pleomorphic - Malignant - Glands adenoma mixed salivary - tumour TUMOURS OF MORE THAN ONE GERM CELL LAYER: .Totipotent cells Mature Immature in gonads or teratoma teratoma in embryonal rests
  • 15.  I. Rate of growth  II. Cancer phenotype and stem cells  III. Clinical and gross features  IV. Microscopic features  V. Local invasion (Direct spread)  VI. Metastasis (Distant spread).
  • 16. Feature Benign Malignant I. CLINICAL AND GROSS FEATURES: 1. Boundaries Encapsulated Irregular 2. Surrounding compressed Invaded 3. Size Small Larger 4. Secondary less often more often changes
  • 17. Feature Benign Malignant II. MICROSCOPIC FEATURES: 1. Pattern : Resembles Poorly- Resemblance 2. Pleomorphism: Not present Present 3. N:C ratio Normal Increase 4. Anisonucleosis Absent Present
  • 18. Feature Benign Malignant III. GROWTH RATE: Slow Rapid IV. LOCAL INVASION:  Benign: Often compresses the surrounding tissues without invading or infiltrating them  Malignant: Usually infiltrates and invades the adjacent tissues.
  • 19. Feature Benign Malignant V. METASTASIS: Absent Present VI. PROGNOSIS: Benign: Local complications. Malignant: Death by local and metastatic complications.
  • 20.  Grade I: Well-differentiated (less than 25% anaplastic cells).  Grade II: Moderately-differentiated (25-50% anaplastic cells).  Grade III: Moderately-differentiated (50-75% anaplastic cells).  Grade IV: Poorly-differentiated or anaplastic (more than 75% anaplastic cells).
  • 21. Men Women Children 1. Lung Breast Acute leukaemia (oral cavity- (cervix in India) in India) 2. Prostate Lung CNS tumour 3. Colorectal Colorectal Bone sarcoma 4. Urinary Endometrial Endocrine bladder  5. Lymphoma Lymphoma Soft tissue sarcoma
  • 22. 1. FAMILIAL AND GENETIC FACTORS. . Multiple endocrine neoplasia (MEN). . Neurofibromatosis . Cancer of the breast: Female relatives of breast cancer patients have 2 to 6 times higher risk of developing breast cancer. .
  • 23. 2. RACIAL AND GEOGRAPHIC FACTORS. i) White Europeans and Americans develop most commonly malignancies of the lung, breast, and colon. ii) Black Africans, on the other hand, have more commonly cancers of the skin, penis, cervix and liver. iii) Japanese have five times higher incidence of carcinoma of the stomach than the Americans.
  • 24. 3. ENVIRONMENTAL AND CULTURAL FACTORS. i) Cigarette smoking : cancer of the oral cavity, pharynx, larynx, oesophagus, lungs, pancreas and urinary bladder. ii) Alcohol: cancer of oropharynx, larynx, oesophagus and liver. iii) Alcohol and tobacco: cancer of the upper aerodigestive tract. iv) Paan in a particular place in mouth for a long time.
  • 25. vii) A large number of industrial and environmental substances are carcinogenic: like arsenic, asbestos, benzene, vinyl chloride, naphthylamine etc. iii) Certain constituents of diet: Overweight individuals, deficiency of vitamin A and people consuming diet rich in animal fats and low in fibre content.
  • 26. IV Pathogens: Human papillomavirus (HPV), EBV or Epstein-Barr virus, hepatitis viruses B and C, Kaposi's sarcoma-associated herpes virus (KSHV), Merkel cell polyomavirus, Schistosoma spp., and Helicobacter pylori; other bacteria are being researched as possible agents.
  • 27.  Fatigue  Lump or area of thickening that can be felt under the skin  Weight changes, including unintended loss or gain  Skin changes, such as yellowing, darkening or redness of the skin, sores that won't heal, or changes to existing moles  Changes in bowel or bladder habits
  • 28.  Persistent cough or trouble breathing  Difficulty swallowing  Hoarseness  Persistent indigestion or discomfort after eating  Persistent, unexplained muscle or joint pain  Persistent, unexplained fevers or night sweats  Unexplained bleeding or bruising
  • 29.  Histopathological  Cytopathological  Haematological  Tumour Marker  Immunohistochemistry(IHC)  Radiological : CT, MRI, PET CT.
  • 30.