Salivary gland tumours

From Ganfyd

(Redirected from Warthin's tumour)
Jump to: navigation, search

Neoplastic lesions of the salivary glands are divided into benign or malignant. Malignant lesions are further divided into primary and secondary.

Contents

Classification

Benign

  • Pleomorphic adenoma
  • Warthin's tumour
  • Monomorphic adenoma
  • Oncocytoma

Malignant

  • Adenoid cystic carcinoma
  • Adenocarcinoma
  • Squamous cell carcinoma
  • Undifferentiated carcinoma
  • Carcinoma expleomorphic adenoma

Variable

  • Mucoepidermoid carcinoma
  • Acinic cell carcinoma

Non epithelial

  • Haemangioma
  • Lymphangioma
  • Neurofibroma
  • Lymphoma

About 80% of salivary gland tumours arise in the parotid gland. 80% of these are benign, 80% are pleomorphic adenoma. One in three tumours in the submandibular gland and one in two in the minor salivary glands are malignant.

Clinical assessment

  • Inspect the mass
  • Inspect the rest of the ears, nose, throat, head and neck
  • Check the cranial nerves (if facial nerve palsy, probably malignant tumour)
  • Fine needle aspiration is 95% sensitive, and is safe
  • Imaging with CT or MRI

Benign tumours

Pleomorphic adenoma

Aetiology

  • Commonest benign salivary tumour
  • Equal sex distribution
  • Peak age of incidence is 50

Pathology

  • Most commonly found in the superficial lobe of the parotid
  • Has a pseudocapsule formed of compressed parotid
  • Arises from several cell types, from intercalated duct cells to myoepithelial cells
  • Has characteristic mixed staining pattern
  • Unknown if they become malignant. Carcinoma expleomorpha adeonoma may or may not arise from a pleomorphic adenoma.

Surgery

  • Aim to preserve the facial nerve using nerve monitoring
  • Pseudocapsule rupture can result in seeding of the tumour
  • Typically, tumour is removed with a surrounding cuff of normal tissue
  • Recurrence is a problem, up to 10% can recurr

Warthin's tumour

Also known as a papillary cystadenoma lymphomatosum or an adenolymphoma.

Aetiology

  • Seven times more frequently in men
  • Peak age of incidence is 70
  • Up to 10% are bilateral

Pathology

  • Arise from heterotropic tissue in lymph nodes within the parotid gland
  • Cystic appearence

Surgery

Same technique as for pleomorphic ademona

  • Much less likely to recurr

Monomorphic adenoma

  • Arise from ductal epithelium
  • Excised with cuff of tissue

Oncocytoma

  • Also known as an Oxyphil adenoma
  • Arises from intralobular ducts
  • Has potential for malignant change
  • Excised with cuff of tissue

Malignant tumours

Malignant tumours of the salivary glands are described using the UICC system.

Tumour
T0 No evidence of primary tumour
T1 Tumour <2 cm, without parenchymal extension
T2 Tumour >2 cm but <4 cm, without parenchymal extension
T3 Tumour 4-6cm or with parenchymal extension, but without facial nerve invovlement
T4 Tumour >6 cm, or invades skull base, or invades facial nerve
T4a No local extension
T4b Local extension involving skin, soft tissue, bone or nerve
Nodes
N0 No regional lymph node metastasis
N1 Metastasis in single ipsilateral node, <3 cm in greatest diameter
N2a Single ispilateral node involvement, 3-6 cm
N2b Multiple ipsilateral node involvement, all <6 cm
N2c Contrlateral or bilateral node involvement, <6 cm
N3 Node involvement >6 cm
Metastasis
M0 No distant metastasis
M1 Distant metastasis

Adenoid cystic carcinoma

Aetiology

  • Commonest malignant salivary tumour
  • Equal sex incidence
  • Peak age of incidence is 60

Pathology

  • More likely to occur in minor salivary glands
  • Slow growning and spreads along nerve sheaths

Surgery

  • Radical excision of tumour and parotid gland
  • Facial nerve may be left behind if unaffected
  • Adjuvant radiotherapy

Adenocarcinoma

  • 3% of parotid tumours
  • 10% of minor salivary gland tumours

Squamous cell carcinoma

  • Rare

Variable tumours

Mucoepidermoid carcinoma

  • Commonest type of salivary tumour to occur in children (but 97% occur in adults)
  • Most ocmmon in parotid gland
  • Low grade tumours behave like benign tumours
  • High grade tumours metastatise early and carry poor prognosis

Acinic cell carcinoma

  • Difficult to classify
  • More benign than mucoepidermoid tumours

Complications of parotid surgery

  • Haemotoma
  • Nerve damage
  • Frey's syndrome
  • Salivary fistula

Temporary nerve paralysis of the facial nerve occurs in 10% of patients. Permenent dysfunction is rare (less than 2%). Frey's syndrome is gustatory sweating.

Salivary tumours in children

Salivary tumours are rare in children, and occur mainly in the parotid. Only 3% of parotid neoplasms occur in patients under 16 years old.

Benign tumours

Mixed tumours are the most common tumours by far. The peak incidence occurs at 10 years old. The behaviour of the tumours is similar to those in adults. Haemangiomas are the next most common tumour.

Malignant tumours

These are very rare. Well differentiated / high grade mucoepidermoid carcinoma is the most common malignant parotid tumour in children.

Personal tools