Category Archives: Cytology

Bethesda System

Bethesda System

Bethesda System in Cervical Vaginal Cytology

Criteria defining specimen adequacy

•    Glass slides must be whole (ie. not broken and unable to be repaired)
•    Clinical information on the patient must be available
•    Slides must have an appropriate label/reference number that is referable to a patient’s identifiers
•    Squamous cells (intermediate squamous cells/metaplastic squamous cells) must be well-preserved and visible—less than 75% of these cells can be obscured by blood, inflammation, air drying, thick areas, poor fixation, contaminants
•    Conventional smears from a cervical sample must contain between 8000-12000 intermediate/metaplastic squamous cells
•    Slides from Thinprep/liquid-based preparations must contain more than 5000 intermediate/metaplastic squamous cells
•    At least 10 columnar/metaplastic cells (from the cervical transitional zone) should be seen—if not, then this must be mentioned in the report
•    Should an epithelial abnormality be seen, it should be reported regardless of specimen adequacy

Bethesda System categories included as squamous epithelial cell abnormalities

•    Atypical squamous cells (of uncertain significance, cannot rule out HSIL—ASC-US, ASC-H)
•    Low grade squamous intraepithelial lesion (LSIL)
•    High grade squmous intraepithelial lesion (HSIL)
•    Invasive squamous cell carcinoma

Terminology

•    Approach to management differs between each of these lesions

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Thyroid Fine Needle Aspiration

Thyroid Fine Needle Aspiration

FNA Thyroid

Criteria for adequacy

•    At least 10 groups/clusters of 10 follicular cells, easily visible (ie. not obscured by blood)

FNA Thyroid Indications

•    Solitary thyroid nodule

•    Dominant nodule in multinodular goitre

Cytologic differences between medullary and papillary thyroid carcinoma

•    Medullary carcinoma usually demonstrates numerous single cells, loose clusters (papillary carcinoma found in sheets, follicles or papillae)

•    Medullary carcinoma shows epithelioid, plasmacytoid, and/or spindle-shaped cells (papillary carcinoma cells are similar to follicular cells)

•    Red cytoplasmic granules (70% of cases) (not seen in papillary carcinoma)

•    Amyloid (not seen in papillary carcinoma)

•    Medullary carcinoma nuclei:

-    round, elongated

-    finely/coarsely granular chromatin (“salt and pepper” nuclei)

-    inconspicuous nucleoli

-    pseudoinclusions (50% of cases) (similar to papillary carcinoma)

-    binucleated or multinucleated

Causes of false positive diagnosis of malignancy

•    Radiation therapy (radioactive iodine: I-131)

•    Follicular adenoma

•    Hyperplastic multinodular goitre

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Urine Cytology

Urine Cytology

Indications for Urine Cytology

Hematuria

Previous positive bladder cytology/history of transitional cell carcinoma (TCC)

High risk of TCC

Cytological findings of Transitional Cell Carcinoma in urine

Large, hyperchromatic, pleomorphic cells with chromatin clumping/coarse, granular chromatin, irregular nuclear membranes, prominent nucleoli

High N:C ratio (>50%)

Dyscohesive clusters, single cells

Dirty, necrotic background

False positive diagnoses causes

Polyoma virus

Instrumentation effect

Lithiasis

Treatment effect (eg. post radiation)

Normal upper tract washings/brushings

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Cytology Histology Discorrelation

Cytology Histology Discorrelation

1.    Wrong patient

2.    False positive on cytology (eg. radiation atypia in biopsy, called HSIL on cytology)

3.    False negative on cytology

4.    Sampling error (cytology and histology are both correct, but neoplastic lesion on histology was missed in sampling for cytology specimen)

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HSIL Mimickers

HSIL Mimickers

1.    Reactive endocervical cells

2.    Radiation atypia

3.    Endometrial cells

4.    Herpes infection

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