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Premanagement in Salivary Gland Tumors

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    Premanagement in

    Salivary Gland TumorsDr Sasikumar SambasivamModerator: Dr Nidhi Patni

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    Anatomy

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    Anatomy

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    y

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    External carotid A

    RetromandibularVein

    Facial NerveSuperficialtemporal A

    MaxillaryA

    P.AuricularA

    Superficialtemporal V

    MaxillaryV

    Post auricularVExternal

    jugularCommon FacialV

    FacialNerve

    temporal

    buccal

    mandibular

    cervical

    zygomatic

    Zygomaticotemporal

    Cervicofacial

    Parotid

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    gland

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    gland

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    Ducts

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    Neural Str.Major Gland Cranial Nerve Foramina of base of skull

    ParotidSuperficial

    Deep

    7

    9,10,11,12

    Stylo mastoid foramen

    Jugular foramen andHypoglossal canal

    Sub mandibular V3,7 (mand and cervical br.),12

    Foramen ovaleStylomastoid foramenHypoglossal canal

    Sub lingual V3 Foramen ovale

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    The Saliva

    Serous (Parotid and Von Ebner)

    Viscous (Sublingual & Minor )

    Mixed (Submandibular &Sublingual)

    Parotid-25 % of total saliva secretion Submandibular-60%

    Sublingual-5%

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    unc onsbriefing

    Saliva

    Anti-Bacterial

    Buffering

    Digestion

    Mineral-

    izationLubricat-ion&Visco-elasticity

    TissueCoating

    Anti-Fung

    al

    Anti

    -Viral

    Carbonic

    anhydrases,Histatins

    Amylases,Mucins,

    Lipase

    Cystatins,

    Histatins,Proline-rich proteins,Statherins

    Mucins,Statherins

    Amylases,Cystatins, Mucins,

    Proline-rich proteins,Statherins

    Histati

    ns

    Cystatins,

    Mucins

    Amylases,

    Cystatins,Histatins,Mucins,Peroxidases

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    ymp o es oParotid

    Peri and Intraparotid Level 1B,2,3, RPnodes; C/L nodes if T crosses midline

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    ofSub Mandibular Level IB

    Level2 Level 3

    Sub Lingual Level IA Level

    1B- Level 2

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    p em o ogy

    3-4% of all H & N neoplasms In gen

    -Parotid>SubMandibular>SubLingual

    Parotid: 80% benign, Submandibular: 50% benign

    Sublingual : Most are malignant

    Age factor:

    Benign: 40 M>F; Malignant: 55yrs M=F

    3% of all in Children ,half are malignant.

    i l

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    Aetiology Unknown

    Radiation Induced(Modan et al)

    Nutritional deficiency(A &C)

    Infection EBV UV rays controversial

    Cigarettes ,Alcohol, hair dyes, higher

    educational level ? Ass. With Breast cancer(2.5 fold

    increase)

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    Pathology

    Benign:

    Pleomorphic Adenoma

    Papillary Cystadenoma Lymphomatosum(Warthin Tumor)

    Benign Lymphoepithelial Lesions (GodwinTumor)

    Oncocytoma

    Basal Cell Adenoma

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    -types(WHO)

    Acinic cell carcinomaMucoepidermoidcarcinomaAdenoid cystic carcinomaPolymorphous LG adenocaEpithelial-myoepithelial

    caBasal cell adenoca

    Sebaceous caPapillary cystadeno caMucinous adeno ca

    Oncocytic carcinomaSalivary duct carcinoma

    Adeno caMyoepithelial ca

    Ca in pleomorphicadenomaSquamous cell

    carcinomaSmall cell carcinoma

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    g Low grade

    Acinic cell ca

    Muco epidermoid (LG)

    High grade

    Mucoepidermoid(HG) ca

    Adeno ca / PD/Anaplastic

    Malignant Mixed

    Adenoid Cystic

    Lymphoepithelioma(Eskimoma)

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    .types :TYPE %

    Parotid (n = 1778 cases)

    Mucoepidermoid 32Adenocarcinoma 16

    Malignant mixed 14

    Adenoid cystic 11

    Acinic 11

    Undifferentiated and squamous 16

    Submandibular (n = 383 cases)

    Adenoid cystic 41

    Acinic 17

    Malignant mixed 12

    Mucoepidermoid 10

    Undifferentiated 9

    Squamous 9

    Adenocarcinoma 2

    Data from Memorial Sloan-Kettering Cancer

    en gn P eomorp ic

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    en gn: P eomorp icadenoma

    Parotid > Sub mandibular

    Painless,slow growing ,Ipsilateral andmore in females

    Has a pseudo capsule; Recurrence after

    excision common 5-10% chance for malignant

    transformationPapillary Cystadenoma

    LymphomatosumWarthin tumor, confined to parotid(Tail)B/L in 10% ;more in older men;Recurrence rare after surgery

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    conditions:Mucoepidermoid ca:

    MC malignancy of SG;90% in parotids f/bHard palate and minor SGs.

    Majority are slow growing

    Most frequent SG tumor in children

    Behavoiur WD vs PD

    Adenocarcinoma:

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    Malignant Mixed Tumors

    From benign conditions like Pas

    Pathlogically carcinosarcomas

    Aggressive behaviour with 20% risk oflocal recc.

    Propensity of LN mets >25%

    Carcinoma Ex Pleomorphic

    Adenoma

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    Adenoid Cystic Carcinoma:

    MC type in Submandibular and Minor SGs

    Solid HP (Undiff)- more malignantbehaviour

    Typical natural history

    LN mets rare(

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    Histology

    Incidence

    AgePredil.(Decade)

    SexPredil.

    Favored Site

    NodeMets

    7thNerveInv.

    Recurr.DistantMets

    Aciniccellcarcinoma

    4 5th F > M Parotid 10 3 10-22 Rare

    Adenoidcystic

    carcinoma

    2-5 5th-6th F = M

    Minor

    salivary15 26 High* 28

    Mucoepidermoidcarcinoma

    Lowgrade

    1st-2nd 8 17

    17-20 4th-5th M > F None 60 33

    Highgrade

    6th High* 75

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    Histology

    Incidence

    AgePredil.(Decade)

    SexPredil.

    Favored Site

    NodeMets

    7thNerveInv.

    RecurrDistantMets

    Malignantmixedtumor

    4 7th M > F

    Parotidandsubmaxillaryglands

    33 14 30-40 31

    Squamous cellcarcinoma

    0.1-3 None None

    Parotidsandsalivaryduct

    High* High* 70 High*

    Adenocarcinoma

    2.8 5th-6th None Parotid 50 9 67 19

    Undifferentiatedcarcinoma

    3 7th-8th F > M None 50 23 High* 30

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    SpreadHistologic Subtypes (%)

    Anaplastic 86

    Epidermoid 21

    Adenocarcinoma 22

    Mucoepidermoid 14

    Malignant mixed 16

    Acinic 2

    Adenoid cystic 2

    Oncocytoma 0

    Data from Armstronget al

    Swellings related

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    Swellings relatedto SGs

    Mucocoele

    Ranula

    Necrotising Sialometaplasia

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    Presentation Painless slow growing mass in most of

    benign.

    1/3rd of parotid ca CN 7 inv. But only10-20 % present with pain

    Multiple CN inv in case of PNI tumors

    Parotid masses mostly in tail.

    Most malignant salivary gland tumors areseen in patients 5060 years old, 2% inchil-dren

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    n ca ors omalignancy

    Facial nerve involvement

    Indurations / ulceration of skin , mucousmembrane

    Lymph node metastasis

    Rapid tumor growth

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    massMetastases to intraparotid nodes/ Lymphoma

    Reactive adenopathy

    Fatty tail of parotid

    Chronic parotitis

    Sarcoidosis

    HIV infection

    Calculus in duct with obstruction

    Neoplasms of mandible

    Cysts (dermoid, bronchial cleft)

    Prominent transverse process of C1 vertebra

    Hemangioma, lipoma, lymphangioma

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    History Local invasion is the initial route

    ,depending on location and histologictype. In Parotid ca -fixation to structuresin 20%.

    Skin invasion is more often seen inparotid tumors (10%), compared withsubmandibular tumors (3%)

    Approximately 25-35% of patients with a

    malignant parotid salivary gland tumorpresent with facial palsy from cranialnerve invasion.

    Lymph node involvement for parotid

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    History LN mets Parotid-18%,SM-28%,

    Tumors from oral cavity presents withcervical node metastases of less than10%.

    Nasopharyngeal SG tumors have a highrisk of occult metastases (50%)

    The risk of + findings in the neck may be

    based on a combination of T-stage andhistology.The highest risk -for SCC, UDC,and salivary duct cancer

    Distant Mets lung>bone >liver.

    k

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    Work up History and clinical examination esp.

    CN,trismus Basic Investigations-CBC , CXR

    FNAC

    CT or *MRI Indications: (1) deep lobeparotid tumors, (2) neurologicallysymptomatic tumors, (3) recurrent

    tumors, and (4) large size (5) Minor SGtumors

    In secondary dep. in SGT -- work up for

    the primary.

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    -Malignancy

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    NX Cannot be assessed

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    N0 No LN mets

    N1 I/L single 3 - 6 cm

    b I/L multiple < = 6 cm

    c B/L, C/L 6 cm

    M0 No Distant Mets

    M1 Distant Mets

    Stage 1 T1 N1 M0

    Stage 2 T2 N0 M0

    Stage 3 T3 N0 MO T1-T3 N1 M0

    Stage 4 A T4a N0/ N1 M0 T1-T4a N2 M0

    Stage 4 B T4b Any N M0 Any T N 3 M0

    Stage 4 C Any T Any N M1

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    Descriptors

    Residual Tumor (R)

    RX: Presence ofresidual tumor

    cannot be assessedR0: No residual

    rognos c

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    rognos cFactors

    Grade , postsurgical residual disease &

    LN status.High grade tumors- 49% LN mets.

    Size of LN

    EC Extn from LN Clinical location of Cervical LN

    ECS -clinical and pathological

    Larger T size & CN inv.--poor prognosis.

    Adenoid cystic, ductal, andundifferentiated carcinoma -highest

    rates of distant mets.

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    on

    Spiro et al. (434 Patients, MSKCC) 90% treated surgically

    Cause specific 5yr cure rate 44%,10y-

    32%,15y-21% Mortality -51% due to original cancer

    Adenoid cystic- poorest prog, about 20%

    surv w/o recurrence Adeno ca- IM outlook, about 35%w/o

    recurrence

    Mucoepidermoid ca-Best control rate, about

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    Thank


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