Week 12 Part 2 - Salivary Glands Continued Flashcards

1
Q

Basal Cell Adenoma

A

Peak incidence 6th decade, major salivary gland
Slow growing - well defined margins
Benign behavior: treatment is complete surgical excision

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2
Q

Basal Cell Adenoma Cytology

A

Numerous monotonous small basaloid cells singly, in cohesive clusters with peripheral palisading
Scanty ill-defined cytoplasm
Dispersed naked nuclei - regular round or oval nuclei, may appear dark but v bland, granular chromatin pattern
Small hyaline globules - scanty fibrous stroma
Squamous whorls if present is a good diagnostic clue, frequent
squamous metaplasia

More images from recorded lecture
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3
Q

Mucoepidermoid Carcinoma

A

Most common of all SG tumours
F>M with a mean age at onset in the 5th decade
MEC is most common SG in children
Symptoms included;
- painless, fixed, slow growing swelling of varying duration
- tenderness
- otorrhea
- dysphagia
- trismus
Treatment is radiotherapy +/- adjunctive therapy

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4
Q

Mucoepidermoid Carcinoma Cytology

A

Dirty background of mucus and debris
See lots of cell in cell engulfment
Clumps and sheets of cells are present with small streams of cells within mucus
Variation in cell type - intermediate, squamous, mucus secreting (most with abundant cytoplasm)
‘Regular’ nuclei with prominent nucleoli and mitoses

First image shows cell in cell engulfment at top of sheet
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5
Q

Adenoid Cystic Carcinoma Overview

A

Peak incidence 5th-7th decade (but can occur in young patients) in both major and minor salivary glands
Second most common SG malignancy in the minor salivary gland
Slow growing, ill defined margins, nerve involvement frequent
Malignant behavior - high local recurrence rate, frequent late metastases; rare solid variants are even more aggressive
Treatment is radical excision +/- adjuvant therapy

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6
Q

Adenoid Cystic Cell Carcinoma - Cytology

A

Epithelial cells – cellular smears
- small uniform, round to oval/some angulation
- globular component (not fibrillary/no matrix)
- cell fragments with finger-like or beaded cords or strands of hyaline stroma
- multilayered dense cell clusters of tumour cells
- scanty cytoplasm, high NC ratio, nuclear molding, naked/stripped nuclei, nucleoli
- relatively uniform round to oval hyperchromatic nuclei with coarse chromatin pattern

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7
Q

Adenoid Cystic Carcinoma Ancillary Testing

A

IHC
- cytokeratins
- epithelial membrane antigen (EMA)
- Sox10
- CD117
- smooth muscle actin (SMA)
- P63
Chromosomal translocation t(6;9)(p22-23;q23-24) resulting in MYB-NF1B fusion

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8
Q

Acinic Cell Carcinoma

A

F>M
Peak 5th and 6th decades; uncommon in kids and
Mainly occurs in the parotid; uncommon in submandibular and minor salivary glands
Slow growing, often circumscribed
Malignant behavior, with moderate metastatic potential
Treatment is radical excision +/- adjuvant therapy

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9
Q

Acinic Cell Carcinoma Cytology

A

Nuclei are round to medium size, uniform, bland, nucleoli variable
Abundant delicate/foamy cytoplasm (PAS positive)
Loose sheets/clusters
Many stripped nuclei in the bg
Cystic bg
Lymphoid population

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10
Q

Acinic Cell Carcinoma IHC

A

Positive for CAM5.2, CK7, DOG1 and SOX10
Negative for P63, CK20 and SMA

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11
Q

Acinic Cell Carcinoma - Pitfalls

A

Normal/hyperplastic salivary acini
Lymphoid rich stroma
Oncocytic neoplasms

Watch recorded lecture for photos

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12
Q

Mammory Analogue Secretory Carcinoma

A

Cellular aspirate
Large polygonal cells in crowded clusters, papillary groups, and single cells
- rounded nuclei with distinct nucleoli
- abundant finely vacuolated cytoplasm with occasional intracytoplasmic mucin containing vacuoles
- absence of cytoplasmic granules
Extracellular mucoid material
- described as filamentous, web-like, or “colloid-like”

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13
Q

Mammory Analogue Secretory Carcinoma IHC

A

Mammaglobin +ve
S100 +ve
GCDFP15 +ve
ETV6-NTRK3 fusion
>90% have translocation
t(12;15)(p13;q25)

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14
Q

Acinic Cell Carcinoma vs MASC

A

Asinic has papillary architecture
Asinic tumour cells bland with granules
MASC can mimic pattern of ACC
MASC cells have more delicate cytoplasm than ACC

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15
Q

Salivary Duct Carcinoma

A

Older adults
Overt malignant features – clearly malignant cells, present singly or in clusters
- pleomorphic nuclei
- necrotic debris
- abundant cytoplasm, squamoid, oncocyte features
- no stromal component
- low grade tumours with a cribriform pattern and uniform cells

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16
Q

Diagnostic Considerations for Differentiating SG Tumours

A

Hyaline globules
Mucinous material
Granular debris
Lymphoid rich
Squamoid
Clear cells
Cystic

17
Q

When are Hyaline Globules Seen?

A

Adenoid cystic ca
Pleomorphic adenoma
Basal cell adenoma/carcinoma
Low grade adenocarcinoma

18
Q

When is a Mucinous Aspriate Seen?

A

Chronic obstructive sialadenitis
Mucoepidermoid carcinoma
Pleomorphic adenoma
Warthin’s tumour

19
Q

When is Granular Debris Seen?

A

Warthin’s tumour
Tumour diathesis
Sialadenitis

20
Q

When is Lymphoid Rich Smear Seen?

A

Warthin’s tumour
Acinic cell carcinoma
Metastasis
Normal lymph node
Lymphoma

21
Q

When is Squamous Morphology Seen?

A

Squamous cell carcinoma
Mucoepidermoid carcinoma
Salivary duct carcinoma
Pleomorphic adenoma
Warthin’s tumour

22
Q

When are Clear Cells Seen?

A

Pleomorphic adenoma
Mucoepidermoid carcinoma
Acinic cell carcinoma
Metastatic

23
Q

When is a Cystic Aspirate Seen?

A

Non-neoplastic
- retention cysts
Warthin’s
Low grade mucoepidermoid carcinoma
Acinic cell carcinoma
Pleomorphic adenoma
Metastasis

24
Q

Metastatic Malignancy

A

> 90% are LNd mets to parotid
- submandibular mets uncommon and almost via haematological spread
80% mets are from head and neck sites
- SCC, Melanoma, Merkel cell carcinoma
Less commonly from other visceral organs
- lung, breast, kidney, prostate

25
Q

Lymphoma

A

Primary involvement of SG parenchyma
- MALT lymphoma most common; may be associated with Sjogrens syndrome
Secondary involvement of intraglandular lymph node
- DLBCL, follicular lymphoma
- Hodgkin Lymphoma
- T cell lymphoma