Cytopathology Flashcards

1
Q

What is cytopathology?

A

The study of cell morphology to establish underlying disease processes

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2
Q

Name some different cytology samples

A
  • Cervical Cytology: NHS Cervical Screening Programme
  • Non-gynaecological samples : Exfoliative samples (brushes, washes, scrapes, fluids) and Fine Needle Aspirates
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3
Q

What happens in the NHS cervical screening programme?

A
  • Women between the ages of 25 – 65 years are invited for screening
  • Repeated every 3-5 years
  • Cervical sample collected into fluid filled bottle, Liquid Based Cytology (LBC)
  • Sample viewed microscopically looking for precancer and cancer cells
  • HR-HPV triage and test of cure testing
  • Future will be primary HR-HPV testing
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4
Q

What is Squamous Dyskaryosis/CIN?

A

Squamous Dyskyosis is defined as abnormal cytologic changes of squamous epithelial cells characterized by hyperchromatic nuclei and/or irregular nuclear chromatin

  • Look for dyskaryosis, pre-cancerous changes in the outermost squamous cells of the cervix
  • Called cervical intraepithelial neoplasia, CIN
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5
Q

What are the different grades of squamous dyskaryosis and their links to cancer?

A
  • There are different grades of CIN according to how severe the changes are, CIN1, CIN2 & CIN3
  • The risk of developing cancer is related to the grade of CIN. Most cases of CIN1 will go back to normal without any treatment.
  • CIN2 and CIN3 may develop into cancer in some cases, if left untreated
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6
Q

Describe Cervical Glandular Intraepithelial Neoplasia (CGIN) as a precursor of cervical adenocarcinoma

A
  • There is a rare abnormality called ‘Cervical Glandular Intraepithelial Neoplasia’ or cGIN
  • This is the pre-cancerous change involving the inner glandular cells of the cervix.
  • Treatment of cGIN is usually the same as CIN.
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7
Q

Describe the NHS cervical screening programme triage when abnormal cells are abnormal?

A
  • Low grade and borderline abnormalities have a HR-HPV test.
  • If HR-HPV positive – refer to colposcopy
  • If HR-HPV negative – routine recall
  • High grade abnormalities refer to colposcopy – no HR-HPV test
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8
Q

What causes CIN? (Cervical intraepithelial neoplasia)

A
  • Human papillomavirus (HPV), family of over 150 viruses
  • Usually don’t cause any problems. When they do, most frequent effect is the common wart, found on the hands and feet
  • About 30 HPV types are spread through genital contact
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9
Q

Describe and identify the low risk type HPV

A
  • About 12 types are called “low risk“
  • They cannot cause cervical cancer. They cause genital warts or very minor cell changes on the cervix.
  • Low-risk types are 6, 11, 40, 42, 43, 44, 53, 54, 61, 72, 73 and 81.
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10
Q

Which types of HPV cause 90% of genital warts?

A

•Types 6 and 11 – cause about 90 percent of genital warts

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11
Q

Describe and identigy high risk type HPV

A
  • Over dozen types of “high-risk” HPV
  • cause abnormal cells to form on the cervix that may develop into cervical cancer if not removed.
  • Of most concern 16, 18, 31, 33, 35, 39, 45, 51, 52, 56, 58, 59 and 68.
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12
Q

Which types of HPV cause 70% of cervical cancers?

A

•Types 16 and 18 cause about 70% of cervical cancers.

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13
Q

Why does some HPV infection lead to cervical cancer? (environmental factors)

A
  • HPV only causes cervical smear abnormalities if it is not cleared from the body over a period of years
  • Smoking can make clearing HPV from the body less effective and can make clearance of minor smear abnormalities slower and less efficient

**About 4 out of 5 adult men and women have had HPV infection at some time in their lives, but only a small minority of women with an HPV infection ultimately have an abnormal smear and a tiny fraction of these get cervical cancer

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14
Q

When is the HPV vaccination given?

A

•Immunisation against HPV started in September 2008 for girls aged 12 to 13 with a catch up for girls up to 18 in the following 3 years

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15
Q

What are two diagnostic/non-gynaecological samples?

A
  • Exfoliative
  • Fine needle aspirations
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16
Q

What is exfoliative cytology and some examples?

A

•This is when cells are dislodged or spontaneously shed from a surface ie.

  • Bronchial washings and brushings, serous cavity effusions such as pleural effusions, ascitic fluid, peritoneal fluid, urine …etc
17
Q

How are fine needle aspirations done?

A
  • If palpable – by hand
  • Radiologist guided – ultrasound, CT
  • Endoscopist – EUS, TBNA, EBUS TBNA
18
Q

What are some common sites for Fine needle aspirations?

A
  • Breast lesions
  • Lung
  • Thyroid
  • Lymph nodes
  • Head and neck lesions
  • Pancreas
  • Deep seated lymph nodes
19
Q

What can fine needle aspirations be used for?

A
  • Immediate on site evaluation
  • Primary diagnosis
  • Rules out other diagnoses
  • Staging
  • Post adjuvant therapy staging
  • Differentiate a new primary from recurrence
20
Q

What are the current applications of Fine needle aspirations?

A
  • Morphologic diagnosis
  • Material for ancillary tests

–Microbiology

–Immunophenotyping

–Flow cytometry

–Molecular studies, mutation analysis

21
Q

Molecular mutation analysis

Match the following genes, which can become mutated, to the cancer

  1. EGFR, ALK-1
  2. BRAF
  3. BRAC1/2, CERB-B2
  4. APC, KRAS
A
  1. EGFR, ALK-1 for lung adenocarcinoma
  2. BRAF for melanoma
  3. BRAC1/2, CERB-B2 for breast cancer
  4. APC, KRAS for colon cancer
22
Q

What are the side effects of fine needle aspiration?

A
  • Typically nothing
  • Bruising
  • Fainting
  • (Pneumothorax – site dependent!)
  • (Infarction of lesion)
23
Q

What are the advantages of cytology fine needle aspiration?

A
  • Accurate
  • Quick
  • Acceptable to patient
  • Rapid turnaround time
  • Organised into fast access clinics run by cytopathologists for aspiration of palpable swellings
  • Cheap
  • Triage material for ancillary tests
  • On-site diagnosis allows immediate patient management