Histopathology 3- Cytopathology Flashcards

1
Q

Name some examples of Gynaecological Cytopathology

A

NHS CSP smears

Diagnostic (symptomatic) smears and endometrial sampling

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2
Q

Name some examples of Non-Gynaecological Cytopathology

A

Cytopathology

Exfoliative (serous effusion, joint, respiratory, GI, CSF)

Aspiration (lymph node, salivary gland, skin and soft tissue masses, cysts, breast, thyroid…)

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3
Q

What is a serous membrane?

A

Connective tissue lined by mesothelial cells

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4
Q

When is a serous effusion pathological?

A

Always

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5
Q

Give some examples of serous membranes

A

Pericardium, Pleura, Abdominal Cavity, Tunica Vaginalis of testis

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6
Q

Describe how a serous effusion is formed

A

Serous membranes well supplied with capillaries - High fluid turnover (up to 10 litres/day)

Formation

  • Hydrostatic pressure in capillaries
  • Oncotic pressure (albumin)
  • Vascular permeability

Resorption - Via lymphatics, capillaries and venules

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7
Q

Describe transudative effusions

A

Plasma ultrafiltrate

‘Mechanical’ –Increased Hydrostatic and decreased Oncotic

Clear, pale yellow, low protein (<3g/dL), doesn’t clot

Single bland degenerate mesothelial cells and a few macrophages and lymphocytes

Usually Benign

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8
Q

List some causes of transudates

A

Cardiac, Cirrhosis, Nephrotic, Hypoproteinemia

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9
Q

Describe exudative effusions

A
  • Unfiltered plasma
  • Changes in vascular permeability
  • Cloudy, yellow or bloody, high protein (>3g/dL), clots
  • Many cells with proteinaceous background
  • Inflammation (infection, infarction, autoimmune)
  • May be malignant
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10
Q

What are mesothelial cells?

A

Mesothelial cells form a monolayer (mesothelium) lining the serosal cavities (pleural, pericardial and peritoneal) and the organs contained within these cavities.

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11
Q

What cells are found in effusions?

A
Mesothelial
Macrophages
Lymphocytes
Eosinophils
Neutrophils
Plasma Cells
Strangers
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12
Q

Describe mesothelial cells in effusions

A
Mesodermal epithelium
Microvilli
Single and grouped
Clusters, balls, papillae, cell-in-cell, indian files
Vary in size
Lacy edges
Windows
Molding
Variable nuclear number, size, N:C ratio
Perinuclear cytoplasmic density
Peripheral lacy border
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13
Q

Describe macrophages in effusions

A
Usually present
Can be difficult to separate from mesothelial cells (esp. degenerate)
Usually single or in loose aggregates
Foamy pale cytoplasm
Eccentric bean shaped nucleus
Lack molding, windows
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14
Q

Describe lymphocytes in effusions

A

Usually a few present

More frequent in longstanding effusions

May be a range of maturation

Lymphocytic effusions are associated with obstructed circulation through lymph nodes and associated with tuberculosis and lymphoma

-part of chronic inflammatory process

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15
Q

Describe neutrophils in effusions

A

Often find a few

If non-infectious may be well preserved

If infectious then often degenerate

If masses then usually benign

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16
Q

What is an LE cells?

Where are they commonly found?

A

A neutrophil or macrophage with an engulfed/phagocytised nucleus

Seen in lupus and AI conditions

17
Q

Describe the malignant cell nuclei?

A

Enlarged

Increased N:C ratio

Irregular membranes

Inclusions

Coarse Irregular

Chromatin

18
Q

Describe the malignant cell cytoplasm?

A

Various vacuoles

Mucin diagnostic (normal cells do not produce mucin therefore it is diagnositic)

Melanin

Keratinisation

19
Q

Malignant mesothelioma

A

Primary malignancy is the context of serous effusions

Asbestos associated

20
Q

Why is fine needle aspiration good for patients? [5]

A
  • Minimal pain and post procedural discomfort
  • Anaesthesia requirement minimal
  • Outpatient procedure
  • Saves time and hospital admission
  • Rapid result
21
Q

Why is FNA good for clinical management?

A
  • Easily repeated allowing sampling of several areas with minimal trauma
  • Minimal disturbance of tissue planes
    Confirms malignancy leaving lesion intact
  • May be therapeutic for cysts and abscesses
  • Quick feedback enables planning of other
  • investigations
    Monitor therapy by repeated sampling
22
Q

Should you air dry of fix the cytology example?

A

Air dry or alcohol fix them

Formalin destroys all formalin so never [only used in human tissue]

23
Q

Why is FNA good for the pathologist?

A
  • Equipment simple and cheap
  • Excellent cell preservation due to rapid fixation
  • Fresh tissue available eg for microbiology or genetic analysis
24
Q

What is granuloma?

A

collection of activated epitheloid histiocytes

25
Q

What are the limitations of FNA?

A

Focality and sampling error

26
Q

What is required for lung cancer diagnosis?

A

Adequate aspirate
Morphologic diagnosis
Immunophenotypic confirmation
Material to permit molecular genetic evaluation (EGFR/ALK)

Small cell v non small cell carcinoma
Squamous cell carcinoma v adenocarcinoma

27
Q

Name a marker of lung adenocarcinoma

A

Napsin positive p63 negative

highly specific of lung adenocarcinoma

28
Q

Name a marker of squamous cell carcinoma of the lung

A

p63 positive