1. Neoplasia

2. Nomenclature Benign: -oma (adenoma, fibroma) Malignant:
carcinoma (epithelial origin)
(adenocarcinoma)
sarcoma (mesenchymal origin)
(fibrosarcoma)

3. Adenoma

4. Adenoma

5. Papilloma

6. Polyp

8. Controlled & Reversible
Non-Neoplastic Proliferation:
Controlled & Reversible
Hypertrophy – Size
Hyperplasia – Number
Metaplasia – Change
Dysplasia – Disordered

9. Neoplastic Proliferation:
Uncontrolled & Irreversible
Benign
Localized, non-invasive.
Malignant (Cancer)
Spreading, Invasive.

10. Dysplasia
Loss of architectural organization and orientation and a loss of cell uniformity in tissue.
Dysplasia is a non-neoplastic proliferation.
Dysplasia may or may not progress to cancer.

11. Here, there is normal cervical squamous epithelium at the left, but dysplastic squamous epithelium at the right. Dysplasia is a disordered growth of epithelium, but still confined to the epithelium. Dysplasia is still reversible.

12. At high magnification, the normal cervical squamous epithelium at the left merges into the dysplastic squamous epithelium at the right in which the cells are more disorderly and have darker nuclei with more irregular outlines.

13. Here is a cervical Pap smear in which dysplastic cells are present that have much larger and darker nuclei than the normal squamous cells with small nuclei and large amounts of cytoplasm.

14. When the entire epithelium is dysplastic and no normal epithelial cells are present, then the process has gone beyond dysplasia and is now neoplasia. If the basement membrane is still intact, as shown here, then the process is called "carcinoma in situ" because the carcinoma is still confined to the epithelium.

15. Differentiation
Rate of growth
Invasion
Metastasis

16. Benign Malignant Slow growing, Enapsulated, Non-invasive
Do not metastasize,
well differentiated,
suffix “oma” eg. Fibroma.
Fast growing,
Not capsulated,
Invasive & Infiltrate
Metastasize.
poorly differentiated,
Suffix “Carcinoma” or “Sarcoma”

19. ANAPLASIA

20. Pleomorphism: variation in size and shape

22. Abnormal nuclear morphology: hyperchormatic (abundant DNA), increased N:C ratio (normal 1:5)

24. Mitoses: increased

25. Here are three abnormal mitoses
Here are three abnormal mitoses. Mitoses by themselves are not indicators of malignancy. However, abnormal mitoses are highly indicative of malignancy. The marked pleomorphism and hyperchromatism of surrounding cells also favors malignancy.

26. Tripolar mitotic figure (abnormal)

28. This sarcoma has many mitoses
This sarcoma has many mitoses. A very large abnormal mitotic figure is seen at the right.

29. Loss of polarity

30. Of course, neoplasms can be benign as well as malignant, though it is not always easy to tell how a neoplasm will act. Here is a benign lipoma on the serosal surface of the small intestine. It has the characteristics of a benign neoplasm: it is well circumscribed, slow growing, non-invasive, and closely resembles the tissue of origin (fat).

31. At low power magnification, a lipoma of the stomach is seen to be well demarcated from the mucosa at the lower center-right. This neoplasm is so well-differentiated that, except for its appearance as a localized mass, it is impossible to tell from normal adipose tissue.

32. Here is the lipoma at high magnification
Here is the lipoma at high magnification. This is a good example of how a benign neoplasm mimics the tissue of origin. These neoplastic adipocytes are indistinguishable from normal adipocytes.

33. This large mass lesion is a liposarcoma
This large mass lesion is a liposarcoma. This one is yellowish, like adipose tissue, and is well-differentiated.

34. This liposarcoma has enough differentiation to determine the cell of origin (adipocyte), but there is still significant pleomorphism of these neoplastic cells (lipoblasts).

35. Benign neoplasms can be multiple, as is shown in this uterus opened anteriorly to reveal leiomyomas of varying size, but all benign and well-circumscribed firm white masses.

36. The microscopic appearance of a leiomyoma indicates that the cells do not vary greatly in size and shape and closely resemble normal smooth muscle cells.

37. Here is a small hepatic adenoma, an uncommon benign neoplasm, but one that shows how well-demarcated a benign neoplasm is. It also illustrates how function of the normal tissue can be maintained, because this adenoma is making bile pigment, giving it a green color with formalin fixation.

38. Hepatic Adenoma
Normal Adenoma

39. This is a squamous cell carcinoma
This is a squamous cell carcinoma. Note the disorderly growth of the squamous epithelial cells in these large nests with pink keratin in the centers. Neoplasms may retain characteristics of their cell of origin.

40. This squamous cell carcinoma demonstrates enough differentiation to tell that the cells are of squamous origin. The cells are pink and polygonal in shape with intercellular bridges (seen as desmosomes or "tight junctions" by electron microscopy). However, the neoplastic cells show pleomorphism, with hyperchromatic nuclei. A mitotic figure is present near the center.

41. This neoplasm is so poorly differentiated that it is difficult to tell what the cell of origin is. It is probably a carcinoma because of the polygonal nature of the cells. Note that nucleoli are numerous and large in this neoplasm.

42. INVASION

43. Malignant neoplasms are characterized by their tendency to invade surrounding tissues. Here, the tan tissue of a lung cancer is seen to be spreading along the bronchi into the surrounding lung. The dark round areas are lymph nodes also involved by the neoplasm.

44. This is a squamous cell carcinoma of the lung
This is a squamous cell carcinoma of the lung. It is a bulky mass that extends into surrounding lung parenchyma.

45. METASTASIS

46. LYMPHATIC Carcinomas Lung – bronchial – tracheobronchial – hilar nodes
UOQ breast – axillary – supra, infraclavicular nodes
Medial breast – internal mammary – supra, infraclavicular nodes

47. HEMATOGENOUS Sarcomas Arteries < veins Portal – liver Caval – lungs
Prostate, thyroid – paravertebral plexus – vertebral column
Renal cell carcinoma – renal vein
Hepatocellular carcinoma – portal vein

48. TRANSCELOMIC
Colon, ovary – peritoneal
Lung – pleural
Brain – CSF

49. Metastatic Adenocarcinoma

50. This is an example of metastases to the liver
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 are the best 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.

51. Microscopically, metastatic adenocarcinoma is seen in a lymph node here. It is common for carcinomas to metastasize to lymph nodes. The first nodes involved are those receiving lymphatic drainage from the site of the primary neoplasm.

52. 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.

53. Epidemiology

54. Pediatric Malignancies
Location
Childhood Malignancy
Blood, marrow, lymph nodes
Leukemia / lymphoma
Adrenal, extra-adrenal ganglia
Neuroblastoma
Cerebellum
Medulloblastoma
Eye
Retinoblastoma
Kidney
Wilms tumor
Bone
Ewing sarcoma

55. Retinoblastoma (white pupil reflex “Leukocoria “)

56. Retinblastoma

57. Multiple adenomatous polyps (tubulovillous adenomas) of the cecum are seen here in a case of familial adenomatous polyposis, a genetic syndrome in which an abnormal genetic mutation leads to development of multiple neoplasms in the colon. The genetic abnormalities present in neoplasms can be inherited or acquired.

58. Carcinogens
Chemical
Radiation
Viral
Bacterial

59. Many chemical carcinogens are related to lifestyle
Chemical agents
Many chemical carcinogens are related to lifestyle
Polycyclic Hydrocarbons
Aromatic amines
Nitroseamines
Aflatoxin B1

60. Radiation
Nuclear radiation
Neck radiation
UV light

61. Viruses Human T-Cell Leukemia Virus Type 1 Human papillomavirus (HPV)
Eptein-Barr virus (EBV)
Human Herpes Virus 8
Hepatitis B,C virus (HBV,HCV)

62. Bacteria
Helicobacter pylori

63. Clinical Manifestations
Paraneoplastic Syndromes
Disruption of tissue integrity
Compression of adjacent structures
Pain
Wasting (Cachexia)
Fatigue
Anemia
Infection

64. Clinical Features of Malignancy
Paraneoplastic Syndromes
10-15% of cancer patients
Symptoms that can’t be explained by spread of the tumor or by indigenous hormones
Endocrinopathies (SIADH, Hypercalcemia)
Vascular and hematologic changes (thrombosis)

65. A paraneoplastic syndrome occurs when a neoplasm elaborates a substance that results in an effect that is not directly related to growth, invasion, or metastasis of the tumor itself.
Sometimes the appearance of the paraneoplastic syndrome may precede diagnosis of the neoplasm and may give a clue to its presence.

66. Paraneoplastic syndromes
Example
Mechanism
Syndrome
Lung (oat cell) carcinoma
ACTH-like substance
Cushing's Syndrome
Lung (squamous cell) carcinoma
Parathormone-like substance
Hypercalcemia
Inappropriate ADH secretion
Hyponatremia
Renal cell carcinoma
Erythropoietin-like substance
Polycythemia
Various carcinomas
Hypercoagulable state
Trousseau's Syndrome
Various carcinomas and sarcomas
Insulin-like substance
Hypoglycemia
Metastatic malignant carcinoid tumors
5-hydroxy-indoleacetic acid (5-HIAA)
Carcinoid Syndrome

67. CACHEXIA Loss of fat and muscle, weakness, anemia, anorexia
Anorexia due to altered sense of taste, central control of appetite
Increased basal metabolic rate
TNF- and IL-1

68. Screening and Diagnosis
Radiographic exams
Lab tests
Biopsy
Grading and staging

69. Here is an example of c-erb-B2 (HER2) positivity of the neoplastic cells in a breast carcinoma. This oncogene acts via reduplication of the normal proto-oncogene hundreds of times, leading to production of a protein product that drives unregulated cell growth. This is detected here by immunohistochemical staining, with the brown reaction product concentrated in a perimembranous pattern around the neoplastic cells.

70. Staging
The most common systems for staging employs the TNM classification. A "T" score is based upon the size and/or extent of invasion. The "N" score indicates the extent of lymph node involvement. The "M" score indicates whether distant metastases are present. Staging forms have been devised for each organ or site that a malignant neoplasm can occur, and the criteria are listed on the form. The forms are filled out using clinical and pathologic criteria and aid in determination of therapy, estimating the prognosis, and developing statistics useful for determining outcomes.

71. Grading
Grading schema are based upon the microscopic appearance of a neoplasm with H&E staining. In general, a higher grade means that there is a lesser degree of differentiation and the worse the biologic behavior of a malignant neoplasm will be. A well-differentiated neoplasm is composed of cells that closely resemble the cell of origin, while poorly differentiated neoplasms have cells that are difficult to recognize as to their cell of origin. Grading schema have been devised for many types of neoplasms, mainly carcinomas. Most grading systems have three or four grades (designated with numbers or roman numerals).

72. Grading and Staging Grade – Microscopic (degree of differentiation)
Stage – Pathologic and clinical findings describing the extend of disease
AJCC Stage – I-IV
Based on T – size and invasiveness of tumor, N – presence or absence of nodal metastases, M – presence or absence of distant metastases
Stage is a stronger predictor of prognosis than grade

73. Moderately differentiated
Grading of Malignant Neoplasms
Definition
Grade
Well differentiated I
Moderately differentiated II
Poorly differentiated
III
Nearly anaplastic IV