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Salivary gland tumours

From Surgopaedia

Epidemiology

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  • F>M
  • Mostly 45-65yo
  • 80% in parotid, 15% submandibular, others in minor salivary glands

Risk factors

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  • Pleomorphic adenoma - radiation
  • Smoking - strong association with Warthin's
  • Viral infections - HIV, EBV, HPV
  • Environmental carcinogens

Aetiology

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  • Benign
    • Pleomorphic adenoma (50% overall, and 80% of parotid)
      • Slow-growing, painless mass, classically in tail of parotid
      • Epithelial, myoepithelial (spindle cell) and stromal cell components
      • Surrounded by fibrous capsule
      • Can transform to malignancy, 10% risk in 15 years
    • Warthin's tumour
      • Papillary cystadenoma lymphomatosum
      • Extremely low incidence of malignant transformation
      • Soft cystic lump
      • Can be either observed or resected
    • Oncocytoma
      • Similar to Warthin's
      • Can excise
    • Cystadenoma
    • Basal cell adenoma
    • Canalicular adenoma
  • Malignant
    • SCC
      • Metastatic SCC is most common in Australia
    • Mucoepidermoid carcinoma
      • Common
      • Invades locally and can recur
      • Variable grade
    • Adenoid cystic carcinoma
    • Acinic cell carcinoma
    • Polymorphous low-grade adenocarcinoma
    • Carcinoma ex pleomorphic adenoma
    • Metastases

Presentation

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  • Usually painless mass
  • Facial nerve paralysis suggests malignancy
  • Cervical lymphadenopathy
    • Parotid usually level II-IV
    • Submandibular usually I-III

Examination

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  • Mass features
  • Trismus
  • Oral cavity
  • Facial nerve examination
  • Cervical LNs
  • Skin or scalp lesions suggestive of primary malignancy

Investigation

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  • USS initially - should also do FNA
    • Milan criteria 1-6 (same as Bethesda system)
  • CNB is more accurate than FNA
  • MRI if soft tissue invasion or nerve involvement suspected
  • CT head/neck/chest
  • PET often done

Staging

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  • TNM
Primary tumor (T)
T category T criteria
TX Primary tumor cannot be assessed
T0 No evidence of primary tumor
Tis Carcinoma in situ
T1 Tumor 2 cm or smaller in greatest dimension without extraparenchymal extension*
T2 Tumor larger than 2 cm but not larger than 4 cm in greatest dimension without extraparenchymal extension*
T3 Tumor larger than 4 cm and/or tumor having extraparenchymal extension*
T4 Moderately advanced or very advanced disease
T4a Moderately advanced disease.

Tumor invades skin, mandible, ear canal, and/or facial nerve.

T4b Very advanced disease.

Tumor invades skull base and/or pterygoid plates and/or encases carotid artery.

* Extraparenchymal extension is clinical or macroscopic evidence of invasion of soft tissues. Microscopic evidence alone does not constitute extraparenchymal extension for classification purposes.
Regional lymph nodes (N)
Pathological N (pN)
N category N criteria
NX Regional lymph nodes cannot be assessed
N0 No regional lymph node metastasis
N1 Metastasis in a single ipsilateral lymph node, 3 cm or smaller in greatest dimension and ENE(–)
N2 Metastasis in a single ipsilateral lymph node, 3 cm or smaller in greatest dimension and ENE(+); or

Larger than 3 cm but not larger than 6 cm in greatest dimension and ENE(–); or

Metastases in multiple ipsilateral lymph node(s), none larger than 6 cm in greatest dimension and ENE(–); or

In bilateral or contralateral lymph nodes, none larger than 6 cm in greatest dimension and ENE(–)

N2a Metastasis in single ipsilateral node 3 cm or smaller in greatest dimension and ENE(+); or

A single ipsilateral node larger than 3 cm but not larger than 6 cm in greatest dimension and ENE(–)

N2b Metastases in multiple ipsilateral nodes, none larger than 6 cm in greatest dimension and ENE(–)
N2c Metastases in bilateral or contralateral lymph node(s), none larger than 6 cm in greatest dimension and ENE(–)
N3 Metastasis in a lymph node larger than 6 cm in greatest dimension and ENE(–); or

In a single ipsilateral node larger than 3 cm in greatest dimension and ENE(+); or

Multiple ipsilateral, contralateral, or bilateral nodes any with ENE(+); or

A single contralateral node of any size and ENE(+)

N3a Metastasis in a lymph node larger than 6 cm in greatest dimension and ENE(–)
N3b Metastasis in a single ipsilateral node larger than 3 cm in greatest dimension and ENE(+); or

Multiple ipsilateral, contralateral, or bilateral nodes any with ENE(+); or

A single contralateral node of any size and ENE(+)

NOTE: A designation of "U" or "L" may be used for any N category to indicate metastasis above the lower border of the cricoid (U) or below the lower border of the cricoid (L).

Similarly, clinical and pathological ENE should be recorded as ENE(–) or ENE(+).

Distant metastasis (M)
M category M criteria
M0 No distant metastasis
M1 Distant metastasis
Prognostic stage groups
When T is... And N is... And M is... Then the stage group is...
Tis N0 M0 0
T1 N0 M0 I
T2 N0 M0 II
T3 N0 M0 III
T0, T1, T2, T3 N1 M0 III
T4a N0, N1 M0 IVA
T0, T1, T2, T3, T4a N2 M0 IVA
Any T N3 M0 IVB
T4b Any N M0 IVB
Any T Any N M1 IVC


Management

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  • Benign
    • Mostly superficial parotidectomy
    • Conservative parotidectomy for small tumours, especially in inferior portion
  • Malignant
    • Resection, including nerve sacrifice if invasion
    • High-grade:
      • Total parotidectomy
      • Adjuvant radiotherapy for high-risk cancers
      • Neck dissection: prophylactic if high-risk factors, or therapeutic if confirmed nodal invasion
    • Low-grade:
      • Superficial parotidectomy
    • Adjuvant chemotherapy role not defined
    • Recurrence:
      • Salvage resection vs radiotherapy vs palliation
      • Palliative systemic therapy has a low response rate