10/3 Flashcards

1
Q

Cancer Nomenclature

A

…oma: benign

…carcinoma: malignant epithelial tumor

…sarcoma: malignant mesenchymal tumor

Blastoma: malignant tumor of embryonic cell of origin (mostly in pediatrics)

Polyps-

  1. Sessile polyp: broad base
  2. Pedunculated polyp: has a stalk at the base
  3. Papillary: rose bud appearance around a central core of fibrous/vascular tissue

Exophytic: extend above epithelial surface

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2
Q

Key Features of Squamous Cell Tumors

A

Intercellular bridges: present in normal epithelium, variable to not evident in cancer

Keratinization: variable to non-existent, hyperkeratotic on surface of whorls, keratin pearls

Dyskeratotic cells: keratinized individual malignant cells, dense eosinophilic staining cytoplasm

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3
Q

Key Features of Adenomatous Neoplasms

A

Benign neoplasms arising from glandular tissue

Colonic adenoma is a polyp, thyroid adenoma is enclosed in a fibrous capsule, hepatic adenoma forms a small irregular mass that is not encapsulated

Hypercellularity and dark staining (hyperchromatic), increased N/C ratio, loss of polarity

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4
Q

Key Features of Adenocarcinomas

A
  1. Glandular: acinar, well to moderate differentiation, glands vary in number and size/shape
  2. Nests: poor differentiation, can be linear cords
  3. Sheets of cells: poor differentiation
  4. Trabecular: poor differentiation
  5. Papillary: variable differentiation, fibrovsscular core
  6. Signet ring: poor differentiation, large cytoplasmic mucin vacuole that pushes the nucleus to the periphery
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5
Q

Cancer Grading and Stage

A

Grade: describes potential aggressiveness, well differentiation is low grade, tumor can contain multiple grades but judge by worst

Stage: describes spread/extent, localized to one area is low stage

Staging is better predictor since considers more far reaching factors

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6
Q

Type of Cancers that Heavily Rely on Grading

A

Prostate

Breast

Ovarian

Renal

Astrocytomas and other types of brain cancer

B cell lymphomas

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7
Q

Gleason Grade and Score

A

Take the two most common tumor grades and add scores together, low of 2 and max of 10

Based on gland formation and architecture

1-2: fairly uniform glands with little stroma between, well differentiated

3: moderately differentiated and still see glands, start to spread out more

4-5: glands grow in back to back fashion and appear as large blobs, tumors can also grow as tiny dots

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8
Q

Bloom-Richardson Grading Scale

A

Grades breast carcinoma

Variables: nuclear grade, mitotic count, tubule formation percentage

Graded from 1-3

Low grade: 3-5
Intermediate grade: 6-7
High grade: 8-9

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9
Q

Cancer Stage

A
  1. Size of the primary lesion (T): T1-4 (T0 is no evidence of tumor), size and local extent of primary lesion measured in cm
  2. Extent of spread to lymph nodes (N): increases as more nodes are involved
  3. Presence/absence of blood borne metastasis
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10
Q

Mesenchymal Tumors

A
  1. Lipoma:circumscription at gross examination, can but don’t have to look different from fat, more eosinophilic between fat drops
  2. Liposarcoma: bunch of ground substance with spindle shaped cells, have lipoblasts that are like fetal fat cells
  3. Fibroma: well circumscribed gray-white tumors on gross examination, hypercellular with spindle shaped nuclei, minimal pleomorphism, and few mitotic figures
  4. Fibrosarcoma: hypercellular, pleomorphic, and increased mitotic figures
  5. Leiomyoma: smooth muscle like in myometrium, hypercellular, spindle shaped cells/nuclei, few mitotic figures and pleomorphism
  6. Leiomyosarcoma: pleomorphism and increased mitotic figures
  7. Chondroma: look similar to normal hyaline cartilage, hypercellularity and some pleomorphism, single or small clusters in blue cartilaginous matrix,have Capillaries while normal hyaline cartilage is avascular
  8. Chondrosarcoma: high N/C ratio, pleomorphism nuclei, hypercellularity and can be within same lacunae, bluish white on gross examination
  9. Osteoid Osteoma: discrete oval on X-ray, reddish brown tissue on gross examination, surrounded by Zone of sclerotic bone
  10. Osteosarcoma: cloudy X-ray, extends into adjacent soft tissue, pleomorphism
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11
Q

Glioblastoma Multiforme

A

Highly pleomorphic tumor that arises from astrocytes, has necrosis

Increased vascularity, leaky blood vessels give rise to cerebral edema

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12
Q

Germ Cell tumors

A

Most often in gonads but can be elsewhere

Teratoma: has tissue of all three germ layers, can be squamous epithelium, sebaceous glands, and cartilage

Can have hair and teeth

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13
Q

Case control study

A

Start in present time, look back to find exposure knowing outcomes like case (diseased) and control (not diseased)

Incident cases are preferred over prevalent cases since prevalence has risk factors that may be more related to survival than disease development

Returns in statistical efficiency diminish dramatically by increasing the control:case ratio beyond 4 or 5

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14
Q

Case Control: Matching

A

Makes sure that cases and controls are similar on certain characteristics

Individual and group matching

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15
Q

Case Control: Biases

A
  1. Selection Bias: need well-defined inclusion/exclusion criteria and sound selection methods to ensure that exposure of cases/controls match exposure from source cohort
  2. Information Bias-
    A. Recall Bias: participants may not be able to accurately exposure info, some cases/controls could be misclassified as exposed/unexposed

B. Interviewer Bias: interviewers might not be blinded to participant status during talks

Exposure status should not be known when a case/control is selected for the study

  1. Confounding Bias: association between exposure and outcome is distorted by the presence of another variable, of confounding is in the source cohort then should be in the study sample to be representative
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16
Q

Case Control: Strengths and Weaknesses

A

Strengths: great for rare diseases (prospective cohort for rare exposures), quick and cheap compared to cohort study, can estimate a causal parameter under certain conditions

Weaknesses: hard to select appropriate controls, info bias, not ideal for rare exposures, hard to establish temporality between exposure/disease