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DR.MAMOON AMEEN
Introduction
Classification
Benign
 Pleomorphic adenoma
 Warthin’s tumor
 Oncocytoma
 Lymphangioma
 Haemangioma
 canalicular adenoma,
 basal cell adenoma
 myoepithelioma
Malignant
• Mucoepidermoid carcinoma
• Adenoid cystic carcinoma
• Carinoma ex- pleomorphic adenoma
• Acinic cell ca
• Adenocarcinoma
• Salivary ductal carcinoma
• Squamous cell carcinoma
• Non-hodgkin’s lymphoma
EPIDEMIOLOGY
 2-3%of all head and neck neoplasms.
 Benign tumors account for 63% to 78% of all salivary gland neoplasms.
 (64%-80%), in the parotid glands ,malignancy (15%- 32%).
 7-11% occur in the submandibular glands, malignancy (37% - 45%).
 less than 1% in the sublingual glands, malignancy (70%-90%),
 9%-23% in the minor glands.
Rule of 80’s:
-80% of salivary gland tumors occur in the parotid
80% of parotid tumors are benign
-80% of parotid tumors are Pleomorphic adenomas
-80% of parotid Pleomorphic adenomas occur in the superficial lobe
-80% of untreated Pleomorphic adenomas remain benign
Etiologic Factors
 Radiation exposure
 Genetic predisposition
 Tobacco
 Chemical carcinogens
 Viruses
PLEOMORPHIC ADENOMA
 Most common of all salivary gland neoplasms
 80-90% of parotid tumors
 Of the minor salivary glands most commonly occurs in the
palate ,upper lip
 4th-6th decades
 M:F = 1:3-4
PLEOMORPHIC ADENOMA
 Slow-growing, painless , firm mass
 Encapsulated
 Mixed tumor: contains both epithelial and mesenchymal elements
 It sends pseudopod-like extensions ‘into surrounding tissue
 Malignant transformation is 10% if observed for more than 15 years.
 Because most of the tumors arise from the superficial lobe, a superficial
parotidectomy is often required.
 Recurrent pleomorphic adenoma is an uncommon but challenging problem.
 There are frequently multiple foci of recurrence that may continue to manifest
over several years.
Warthin’s tumor(papillary cystadenoma lymphomatosum )
 2nd most common after pleomorphic adenoma
 Commonly seen 7th decade
 Male: female (7:1)
 Associated with cigarette smoking
 Almost Exclusively in parotid gland Parotid tail
 10% bilateral
 Usually Fluctuant, slow growing
 Encapsulated cystic lesion
 Histologically: epithelial & lymphoid elements
 Never malignant
 Wide local excision
 parotidectomy with facial nerve preservation
Oncocytoma (oxyphil adenoma)
 Rare 1 % of benign salivary tumor
 6th decade
 No gender predilection
 Parotid ,Submandibular gland
 Minor salivary glands: palate, buccal mucosa,
 Slow growing ,painless
 The treatment of choice for is surgical excision.
Malignant neoplasms
 Shorter duration
 Grow rapidly or history of slow growth with sudden rapid activity
 Fixed to surrounding tissues
 Overlying skin or mucous membrane may be ulcerated or inflamed
 Surface telangiectasia
 Nerve involvement
 Regional lymph nodes may be enlarged
Mucoepidermoid Carcinoma
 2nd most common salivary gland tumor
 Most common salivary gland malignancy
 Parotid 80% - 90% of cases
 Age: 5th – 7th decades
 Gender: slight female predilection
 Site: parotid gland, palate
 Etiology: radiation exposure
 It contain two major elements:
 mucin producing cells & epithelial cells of epidermoid variety & according to that classified into
Low grade
Intermediate
High grade
 Low-grade: slow growing, painless mass
 High-grade: rapidly enlarging, +/- pain
Adenoid cystic carcinoma(Cylindroma)
 2nd most common salivary gland malignancy
 Infiltrates widely into the tissue planes & muscles
 Perineural spread
 Commonly in submandibular gland, sublingual or minor salivary glands
 Slow growing but aggressive neoplasm with a remarkable capacity of recurrence.
 Infrequent cervical metastases
 High degree of late distant metastases
 Treatment
 Complete local excision
 Tendency for perineural invasion: facial nerve sacrifice
 Postoperative RT
 Prognosis
 Local recurrence: 42%
 Indolent course: 5-year survival 75%, 20-year survival 13%
ACINIC CELL CARCINOMA
 6% to 8% of all salivary malignancies
 Mostly in parotid
 3% Shows bilateral involvement
 Has a low-grade behavior
 Associated with the best survival rate of any salivary malignancy
ACINIC CELL CARCINOMA
 They seldom metastasize but they have high tendency to recur locally
 Primary treatment is complete surgical resection with neck dissection limited to the therapeutic
setting.
 Postoperative radiation is not routinely advised
Carcinoma ex-pleomorphic adenoma
 Malignant degeneration can occur in 3% to 7 % of
pleomorphic adenomas.
 Parotid > submandibular > palate
 Risk of malignant degeneration
 1.5% in first 5 years
 9.5% after 15 years
 Typical history of slowly growing mass demonstrating sudden increase in
the growth.
 Treatment
 Radical excision
 Neck dissection (25% with lymph node involvement at presentation)
 Postoperative XRT
 Polymorphous Low-Grade Adenocarcinoma
 2ND most common malignant intraoral tumor of the salivary glands.
 Palate (60-70%) > buccal mucosa (16%) > upper lip, retromolar area,
base of tongue.
 F:M = 2:1 & common in 5th to 7th decade.
 A painless mass in the palate is the most common presentation.
SALIVARY DUCT CARCINOMA
 High grade aggressive tumor
 from excretory duct cells in major salivary gland mainly
 Microscopic feature remarkably similar to mammary intraductal carcinoma
 35% recurrence
 62% distant metastasis
 Neural invasion and extraglandular extension are commonly seen.
 Most patients die within three years.
SALIVARY DUCT CARCINOMA
ADENOCARCINOMA:
 Ranging from low grade well differentiated to high grade invasive lesions
 Common in major glands
 Originate from excretory or striated ducts
 Cystic or solid, may be papillary or non-papillary in growth pattern
 Prognosis depend on grade
SQUAMOUS CELL CARCINOMA
 Rare to be primary & common to be secondary from intraparotid lymph node or direct
involvement
 Should be differentiated from mucoepidermoid carcinoma by presence of mucin on
electronmicroscope with stain or immunohistochemical test
 Incidence 0.3% -1.5% in major gland 50% nodal metastasis
 M:F = 2:1
 7th-8th decades
 TR: Surgery + Neck dissection + Postop. RT
LYMPHOMA:
 5% of all extranodal lymphoma affect salivary gland
 90% occur in parotid
 85% are N H L
 Its risk in Sjogren’s syndrome is 44 fold higher
SECONDARY TUMORS:
 The majority of metastasis are caused by lymphatic spread from cutaneous
malignancy of the head & neck
 Hematogenous metastasis are rare & majority from lung, kidney & breast
 Contiguous extension of facial sarcomas
 10% of malignant parotid gland tumors
 40% are SCC, & 40% are melanoma
STAGING
STAGING:
Stage I T1N0M0
Stage II T2N0M0
Stage III T3N0M0 or T1-3 N1M0
Stage IVA T4aN0-1M0 or T1-4a N2M0
Stage IVB T4bNxM0 or TxN2-3M0
Stage IVC TxNxM1
Evaluation of patient
History Important points in the history
 Mass (duration, rate of the growth, presence of pain)
 Facial paralysis, B/L
 Cervical lymphadenopathy
 Eyes and joints symptoms
 H/O exposure to radiation
 Ipsilateral weakness or numbness of tongue
Examination:-
 Size of the mass
 Overlying skin, Skin fixation, mobility
 Lymphadenopathies
 Cranial nerves
 Intraoral examination
Investigations
 USG
 X ray chest
 OPG To R/O mandibular involvement.
 CT SCAN
 MRI
USG
 Distinguish intrinsic from extrinsic tumors
 It can be used to differentiate solid from cystic masses in the salivary glands
 USG guided FNAC
CT/MRI
 Anatomical localization
 Local, regional ,distant invasion
MRI IS BETTER ??
 Excellent assessment of margins
 Deep extension and infiltration
 Bone marrow invasion
 Perineural spread
 Intracranial extension
Fine-Needle Aspiration Biopsy
 Accuracy well established
 Sensitivity = 54-95%
 Specificity = 86 - 100%
 Confirms possibility
 Lymphoma/inflammatory masses.
 Allows preoperative assesment of
 Nature of tumour
 Extent of resection (conservative/radical)
 Management of facial nerve (high grade adenoid cystic)
 Likelihood of neck dissection (high grade).
Open biopsy
 Contraindicated
 Justified in minor salivary gland tumor
 Ulcerated lesion
 where fine needle aspiration cytology suggests lymphoma,
 In cases of diffuse salivary enlargement
Frozen section
 may be useful when
 preoperative FNA is non-diagnostic,
 when the FNA diagnosis is at odds with the clinical and/or intraoperative findings
 The results of frozen section may help in intraoperative decision-making. In cases where frozen
section shows high-grade carcinoma, the surgeon may proceed to perform at least a limited neck
dissection with the parotidectomy
MANAGEMENT
 TREATMENT
 Surgery
 Radiotherapy
 Chemotherapy
 Factors that influence treatment
 Age
 Metastatic spread
 Facial nerve involvement
 Mandibular / Temporal bone involvement
 Skin
 Site of tumor
 Size, Extent, Grade & stage
 Benign salivary gland tumors should be excised completely with an adequate margin to avoid local
recurrences
 Simple enucleation not appropriate treatment recurrence rate 21-45%
 1 cm margin has been shown to be adequate.
 Cutting into the tumour should be absolutely avoided as it can lead to tumor spillage
Surgery
Benign tumors
Surgery
Benign tumors
 Superficial parotidectomy
 partial superficial parotidectomy,
 Deep lobe tumors -Total parotidectomy with facial nerve preservation.
 Parapharyngeal tumors -cervical-parotid approach and with or without a mandibulotomy.
Surgery
Benign tumors
 A tumor of the submandibular gland requires submandibular gland resection
 If the tumor originates from a minor salivary gland, the tumor and a cuff of normal
tissue should be excised.
Surgery
Malignancies
 The mainstay of treatment for salivary carcinomas is surgical resection with or without postoperative
radiotherapy
 The extent of surgery is dependent on the size and site of the tumour
 The goal of surgical treatment is to achieve local control
 As a general rule, every effort should be made to preserve a nerve which was functioning normally
preoperatively
Surgery
Facial nerve sacrifice should be reserved for cases of
 preoperative paralysis,
 cases of recurrent malignancy
 gross encasement and infiltration of the nerve
Surgery
Parotid Gland:
 Size and location determine extent of resection
 Most T1/T2 lesions lateral to the nerve are suitable for a superficial parotidectomy with adequate
margin 1.5cm
 Larger and deep lobe tumours usually require a total conservative parotidectomy with preservation of
the facial nerve
 Patients with high grade and extensive disease (i.e. skin involvement or facial palsy) may require
extended radical parotidectomy
Superficial parotidectomy:
Removal of superficial lobe of the parotid
(superficial to facial nerve)
RADICAL PAROTIDECTOMY
 Removal of
 Both lobes of parotid
 Facial nerve
 Mandibular ramus
 Masseter muscle
 Infratemporal fossa dissection
 Subtotal petrosectomy
Complications of parotid surgery
 Facial nerve injury
 HEMATOMA
 Salivary fistulas
 Infection : Flap necrosis is common
 Frey’s syndrome
 Sialocele
 Numbness over the face and ear
Neck dissection
 Neck dissection should be performed in patients with clinical or radiological evidence of nodal disease
 A prophylactic selective neck dissection should be considered for patients with high-stage or high-
grade
Radiotherapy
 Primary treatment for salivary carcinomas is limited to unresectable tumours
 Postoperative radiotherapy is indicated for:
 Tumours greater than 4 cm,
 Presence of positive surgical margins or
 Facial nerve were preserved despite being adherent to the tumour,
 lymph node metastases
 High grade tumor
 perineural invasion.
 Recurrent pleomorphic adenoma
 Spillage after surgery for pleomorphic adenoma
Radiotherapy
 Preoperative radiotherapy
Given in large tumours to reduce the size and make it better operable, i.e. to down stage the disease
Prognosis
 Advanced stage, higher histologic grade _____poor prognosis
 submandibular location _____________________poorer outcome
 10 yr survival rates for stage I ____82%
II____ 64%
III ____50%
IV ____33%
 Regional lymph node metastases ______poorer prognosis
Prognosis
 Distant metastases _________________ poor prognosis
 Parapharyngeal space extension _____poor prognosis
 Parotid malignancies ________________ better prognosis
 Facial nerve paralysis ________________ poor prognosis
Salivary gland tumor

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Salivary gland tumor

  • 3. Classification Benign  Pleomorphic adenoma  Warthin’s tumor  Oncocytoma  Lymphangioma  Haemangioma  canalicular adenoma,  basal cell adenoma  myoepithelioma Malignant • Mucoepidermoid carcinoma • Adenoid cystic carcinoma • Carinoma ex- pleomorphic adenoma • Acinic cell ca • Adenocarcinoma • Salivary ductal carcinoma • Squamous cell carcinoma • Non-hodgkin’s lymphoma
  • 4. EPIDEMIOLOGY  2-3%of all head and neck neoplasms.  Benign tumors account for 63% to 78% of all salivary gland neoplasms.  (64%-80%), in the parotid glands ,malignancy (15%- 32%).  7-11% occur in the submandibular glands, malignancy (37% - 45%).  less than 1% in the sublingual glands, malignancy (70%-90%),  9%-23% in the minor glands.
  • 5. Rule of 80’s: -80% of salivary gland tumors occur in the parotid 80% of parotid tumors are benign -80% of parotid tumors are Pleomorphic adenomas -80% of parotid Pleomorphic adenomas occur in the superficial lobe -80% of untreated Pleomorphic adenomas remain benign
  • 6. Etiologic Factors  Radiation exposure  Genetic predisposition  Tobacco  Chemical carcinogens  Viruses
  • 7. PLEOMORPHIC ADENOMA  Most common of all salivary gland neoplasms  80-90% of parotid tumors  Of the minor salivary glands most commonly occurs in the palate ,upper lip  4th-6th decades  M:F = 1:3-4
  • 8. PLEOMORPHIC ADENOMA  Slow-growing, painless , firm mass  Encapsulated  Mixed tumor: contains both epithelial and mesenchymal elements  It sends pseudopod-like extensions ‘into surrounding tissue  Malignant transformation is 10% if observed for more than 15 years.
  • 9.  Because most of the tumors arise from the superficial lobe, a superficial parotidectomy is often required.  Recurrent pleomorphic adenoma is an uncommon but challenging problem.  There are frequently multiple foci of recurrence that may continue to manifest over several years.
  • 10. Warthin’s tumor(papillary cystadenoma lymphomatosum )  2nd most common after pleomorphic adenoma  Commonly seen 7th decade  Male: female (7:1)  Associated with cigarette smoking  Almost Exclusively in parotid gland Parotid tail  10% bilateral
  • 11.  Usually Fluctuant, slow growing  Encapsulated cystic lesion  Histologically: epithelial & lymphoid elements  Never malignant  Wide local excision  parotidectomy with facial nerve preservation
  • 12. Oncocytoma (oxyphil adenoma)  Rare 1 % of benign salivary tumor  6th decade  No gender predilection  Parotid ,Submandibular gland  Minor salivary glands: palate, buccal mucosa,  Slow growing ,painless  The treatment of choice for is surgical excision.
  • 13. Malignant neoplasms  Shorter duration  Grow rapidly or history of slow growth with sudden rapid activity  Fixed to surrounding tissues  Overlying skin or mucous membrane may be ulcerated or inflamed  Surface telangiectasia  Nerve involvement  Regional lymph nodes may be enlarged
  • 14. Mucoepidermoid Carcinoma  2nd most common salivary gland tumor  Most common salivary gland malignancy  Parotid 80% - 90% of cases  Age: 5th – 7th decades  Gender: slight female predilection  Site: parotid gland, palate  Etiology: radiation exposure
  • 15.  It contain two major elements:  mucin producing cells & epithelial cells of epidermoid variety & according to that classified into Low grade Intermediate High grade  Low-grade: slow growing, painless mass  High-grade: rapidly enlarging, +/- pain
  • 16. Adenoid cystic carcinoma(Cylindroma)  2nd most common salivary gland malignancy  Infiltrates widely into the tissue planes & muscles  Perineural spread  Commonly in submandibular gland, sublingual or minor salivary glands  Slow growing but aggressive neoplasm with a remarkable capacity of recurrence.
  • 17.  Infrequent cervical metastases  High degree of late distant metastases  Treatment  Complete local excision  Tendency for perineural invasion: facial nerve sacrifice  Postoperative RT  Prognosis  Local recurrence: 42%  Indolent course: 5-year survival 75%, 20-year survival 13%
  • 18. ACINIC CELL CARCINOMA  6% to 8% of all salivary malignancies  Mostly in parotid  3% Shows bilateral involvement  Has a low-grade behavior  Associated with the best survival rate of any salivary malignancy
  • 19. ACINIC CELL CARCINOMA  They seldom metastasize but they have high tendency to recur locally  Primary treatment is complete surgical resection with neck dissection limited to the therapeutic setting.  Postoperative radiation is not routinely advised
  • 20. Carcinoma ex-pleomorphic adenoma  Malignant degeneration can occur in 3% to 7 % of pleomorphic adenomas.  Parotid > submandibular > palate  Risk of malignant degeneration  1.5% in first 5 years  9.5% after 15 years  Typical history of slowly growing mass demonstrating sudden increase in the growth.
  • 21.  Treatment  Radical excision  Neck dissection (25% with lymph node involvement at presentation)  Postoperative XRT
  • 22.  Polymorphous Low-Grade Adenocarcinoma  2ND most common malignant intraoral tumor of the salivary glands.  Palate (60-70%) > buccal mucosa (16%) > upper lip, retromolar area, base of tongue.  F:M = 2:1 & common in 5th to 7th decade.  A painless mass in the palate is the most common presentation.
  • 23. SALIVARY DUCT CARCINOMA  High grade aggressive tumor  from excretory duct cells in major salivary gland mainly  Microscopic feature remarkably similar to mammary intraductal carcinoma  35% recurrence  62% distant metastasis  Neural invasion and extraglandular extension are commonly seen.  Most patients die within three years.
  • 25. ADENOCARCINOMA:  Ranging from low grade well differentiated to high grade invasive lesions  Common in major glands  Originate from excretory or striated ducts  Cystic or solid, may be papillary or non-papillary in growth pattern  Prognosis depend on grade
  • 26. SQUAMOUS CELL CARCINOMA  Rare to be primary & common to be secondary from intraparotid lymph node or direct involvement  Should be differentiated from mucoepidermoid carcinoma by presence of mucin on electronmicroscope with stain or immunohistochemical test  Incidence 0.3% -1.5% in major gland 50% nodal metastasis  M:F = 2:1  7th-8th decades  TR: Surgery + Neck dissection + Postop. RT
  • 27. LYMPHOMA:  5% of all extranodal lymphoma affect salivary gland  90% occur in parotid  85% are N H L  Its risk in Sjogren’s syndrome is 44 fold higher
  • 28. SECONDARY TUMORS:  The majority of metastasis are caused by lymphatic spread from cutaneous malignancy of the head & neck  Hematogenous metastasis are rare & majority from lung, kidney & breast  Contiguous extension of facial sarcomas  10% of malignant parotid gland tumors  40% are SCC, & 40% are melanoma
  • 30. STAGING: Stage I T1N0M0 Stage II T2N0M0 Stage III T3N0M0 or T1-3 N1M0 Stage IVA T4aN0-1M0 or T1-4a N2M0 Stage IVB T4bNxM0 or TxN2-3M0 Stage IVC TxNxM1
  • 31. Evaluation of patient History Important points in the history  Mass (duration, rate of the growth, presence of pain)  Facial paralysis, B/L  Cervical lymphadenopathy  Eyes and joints symptoms  H/O exposure to radiation  Ipsilateral weakness or numbness of tongue
  • 32. Examination:-  Size of the mass  Overlying skin, Skin fixation, mobility  Lymphadenopathies  Cranial nerves  Intraoral examination
  • 33. Investigations  USG  X ray chest  OPG To R/O mandibular involvement.  CT SCAN  MRI
  • 34. USG  Distinguish intrinsic from extrinsic tumors  It can be used to differentiate solid from cystic masses in the salivary glands  USG guided FNAC
  • 35. CT/MRI  Anatomical localization  Local, regional ,distant invasion MRI IS BETTER ??  Excellent assessment of margins  Deep extension and infiltration  Bone marrow invasion  Perineural spread  Intracranial extension
  • 36.
  • 37.
  • 38.
  • 39.
  • 40. Fine-Needle Aspiration Biopsy  Accuracy well established  Sensitivity = 54-95%  Specificity = 86 - 100%  Confirms possibility  Lymphoma/inflammatory masses.  Allows preoperative assesment of  Nature of tumour  Extent of resection (conservative/radical)  Management of facial nerve (high grade adenoid cystic)  Likelihood of neck dissection (high grade).
  • 41. Open biopsy  Contraindicated  Justified in minor salivary gland tumor  Ulcerated lesion  where fine needle aspiration cytology suggests lymphoma,  In cases of diffuse salivary enlargement
  • 42. Frozen section  may be useful when  preoperative FNA is non-diagnostic,  when the FNA diagnosis is at odds with the clinical and/or intraoperative findings  The results of frozen section may help in intraoperative decision-making. In cases where frozen section shows high-grade carcinoma, the surgeon may proceed to perform at least a limited neck dissection with the parotidectomy
  • 43. MANAGEMENT  TREATMENT  Surgery  Radiotherapy  Chemotherapy  Factors that influence treatment  Age  Metastatic spread  Facial nerve involvement  Mandibular / Temporal bone involvement  Skin  Site of tumor  Size, Extent, Grade & stage
  • 44.  Benign salivary gland tumors should be excised completely with an adequate margin to avoid local recurrences  Simple enucleation not appropriate treatment recurrence rate 21-45%  1 cm margin has been shown to be adequate.  Cutting into the tumour should be absolutely avoided as it can lead to tumor spillage Surgery Benign tumors
  • 45. Surgery Benign tumors  Superficial parotidectomy  partial superficial parotidectomy,  Deep lobe tumors -Total parotidectomy with facial nerve preservation.  Parapharyngeal tumors -cervical-parotid approach and with or without a mandibulotomy.
  • 46. Surgery Benign tumors  A tumor of the submandibular gland requires submandibular gland resection  If the tumor originates from a minor salivary gland, the tumor and a cuff of normal tissue should be excised.
  • 47. Surgery Malignancies  The mainstay of treatment for salivary carcinomas is surgical resection with or without postoperative radiotherapy  The extent of surgery is dependent on the size and site of the tumour  The goal of surgical treatment is to achieve local control  As a general rule, every effort should be made to preserve a nerve which was functioning normally preoperatively
  • 48. Surgery Facial nerve sacrifice should be reserved for cases of  preoperative paralysis,  cases of recurrent malignancy  gross encasement and infiltration of the nerve
  • 49. Surgery Parotid Gland:  Size and location determine extent of resection  Most T1/T2 lesions lateral to the nerve are suitable for a superficial parotidectomy with adequate margin 1.5cm  Larger and deep lobe tumours usually require a total conservative parotidectomy with preservation of the facial nerve  Patients with high grade and extensive disease (i.e. skin involvement or facial palsy) may require extended radical parotidectomy
  • 50. Superficial parotidectomy: Removal of superficial lobe of the parotid (superficial to facial nerve)
  • 51.
  • 52.
  • 53.
  • 54.
  • 55. RADICAL PAROTIDECTOMY  Removal of  Both lobes of parotid  Facial nerve  Mandibular ramus  Masseter muscle  Infratemporal fossa dissection  Subtotal petrosectomy
  • 56. Complications of parotid surgery  Facial nerve injury  HEMATOMA  Salivary fistulas  Infection : Flap necrosis is common  Frey’s syndrome  Sialocele  Numbness over the face and ear
  • 57. Neck dissection  Neck dissection should be performed in patients with clinical or radiological evidence of nodal disease  A prophylactic selective neck dissection should be considered for patients with high-stage or high- grade
  • 58. Radiotherapy  Primary treatment for salivary carcinomas is limited to unresectable tumours  Postoperative radiotherapy is indicated for:  Tumours greater than 4 cm,  Presence of positive surgical margins or  Facial nerve were preserved despite being adherent to the tumour,  lymph node metastases  High grade tumor  perineural invasion.  Recurrent pleomorphic adenoma  Spillage after surgery for pleomorphic adenoma
  • 59. Radiotherapy  Preoperative radiotherapy Given in large tumours to reduce the size and make it better operable, i.e. to down stage the disease
  • 60. Prognosis  Advanced stage, higher histologic grade _____poor prognosis  submandibular location _____________________poorer outcome  10 yr survival rates for stage I ____82% II____ 64% III ____50% IV ____33%  Regional lymph node metastases ______poorer prognosis
  • 61. Prognosis  Distant metastases _________________ poor prognosis  Parapharyngeal space extension _____poor prognosis  Parotid malignancies ________________ better prognosis  Facial nerve paralysis ________________ poor prognosis

Editor's Notes

  1. Haemangioma: Most common benign tumors of the parotid in children
  2. Parotid: usually arises from its tail, deep lobe
  3. associated with cigarette smoking, which may be due to irritation of the ductal epithelium by tobacco smoke that initiates tumorigenesis
  4. Pleomorphic adenoma
  5. Warthins tumor
  6. Mucoepidermoid ca
  7. Adenoid cystic ca Perineural spread mandibular nerve
  8. Strip the superfacial lobe off the branches of the facial nerve
  9. Completed superfacial parotidectomy