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Tumours of Pharynx
Tumours of Nasopharynx
 BENIGN TUMOURS
 Juvenile Nasopharyngeal Angiofibroma (mc)
 Craniopharyngioma
 Rhabdomyoma
 Teratoma, Paraganglioma
 Chondroma, Chordoma
 Hamartoma, Haemangioma
 Pleomorphic adenoma, Warthin’s tumour
Juvenile Nasopharyngeal Angiofibroma
 Histologically benign but locally aggressive vascular tumour occupying nasopharynx seen in
adolescent males causing recurrent unprovoked episodes of epistaxis
 Incidence 0.05 to 0.1% of head & neck cancers
 Etiology
 Age gp – 10 – 25 years of age, adolescents (mc), regresses/ stops growing after 25 yrs of age
 Sex – males (exclusive)
 Nasal erectile vascular tissue(hamartomatous nidus of inf turbinate tissue) mislocated in
nasopharynx -> gets activated when testosterone acts on it -> NPA
 Abnormal growth of nasopharyngeal fibrocartilage/ fibrovascular stroma
 Origin from non chromaffin preganglionic cells of terminal branches of maxillary artery
 Genetic/ Heredity
 Trauma
 Infection
 Allergy
 Pathology
 Contains both vascular and fibrous tissue
 Covered with nasopharyngeal mucosa – deceives vascularity
 Pink grey or purple red colour, sessile or pedunculated
 No capsule – invades locally
 Thin walled vessels just endothelial lined, no muscular coat – bleeding which cant be controlled by
adrenaline
 Extension
 Origin – above sup margin of sphenopalatine foramen in lat wall of nasopharynx,
attached to roof of choana, post part of middle turbinate, post part of nasal septum
 Locally invasive
 Anteriorly – nasal cavity, orbit
 Posteriorly – destroys pterygoid plates, extends to vidian nerve
 Superiorly – sphenoid sinus->cavernous sinus, middle cranial fossa
 Sphenoid sinus -> post ethmoids, ant cranial fossa
 Laterally -> pterygopalatine fossa -> maxillary sinus -> infratemporal fossa -> cheek
 Clinical features
 Nasal
 U/L gradually increasing nasal obstruction, later B/L
 Recurrent painless unprovoked episodes of nasal bleed
 Nasal discharge
 Loss of smell
 Mouth breathing/ snoring
 Rhinolalia clausa
 Ear
 Blockage in ear due to ET blockage leading to serous otitis media and conductive hearing loss,
otalgia, tinnitus
 Eyes
 Pain, proptosis, lacrimation, diplopia, rarely blindness
 Face
 Cheek swelling, broadening of nasal bridge, frog face deformity
 CNS
 II CN – blindness
 III, IV, VI CN – diplopia
 V CN – neuralgic pain
 Increased intracranial pressure – headache, blurring of vision, projectile vomiting
 General – Anaemia, sexual underdevelopment
 NO LYMPH NODE INVOLVEMENT
 Signs
 Post rhinoscopy
 Pink, purple, reddish globular sessile lobulated mass, firm in consistency obstructing
one or both choana, may be visible below nasopharyngeal isthmus
 Ant rhinoscopy
 Globular pinkish mass in post part of nasal cavity, septum deviated to opposite side
 NO PROBE TEST, NO DIGITAL PALPATION
 Oral cavity – soft palate bulge
 D/D – Infected AC polyp, carcinoma, rhinosporodiosis, craniopharyngioma
 Diagnosis
 Clinical
 DNE
 Biopsy – Only excision biopsy
 Radiology
 X ray soft tissue nasopharynx lateral view – soft tissue in NP
 CT Scan with contrast – gold standard
 Vascular dumb bell shaped tumour in nasal cavity, nasopharynx, pterygopalatine foramen
 Anterior bowing of posterior wall of maxillary sinus and post bowing of pterygoids – Holman Miller sign/
Antral sign
 MRI – intracranial/ orbit extension
 Digital Subtraction Angiography (DSA)/ Carotid angiography
 Tumour can be seen
 Also used to embolise feeding vessel on same side – internal maxillary artery
 Materials used – gelfoam, PVA
 Helps to reduce bleeding intraoperatively
 Operate 24- 48 hours after embolization
 Always arrange blood transfusion before surgery
 Other methods to reduce bleeding – estrogen therapy, pre op RT, cryotherapy
 Staging Sessions/ Fisch ()
 I A – limited to nasopharynx and nose (I)
 I B – Extend to PNS (II)
 II A – Minimal extension to pterygomaxillary fossa (II)
 II B – Full occupation of pterygomaxillary fossa with bony erosion of orbit (II)
 III A – Erosion of skull base with minimal intracranial extension (III)
 III B – Extensive intracranial extension with extending to cavernous sinus, optic
chiasma, pituitary fossa (IV)
 Treatment
 Surgical excision – TOC
 Complete excision
 Approaches
 Wilson’s transpalatal approach – Preferred if tumour limited to nose and nasopharynx – U
incision made at the junction of soft and hard palate – separation of hard and soft palate – part
hard palate removed for better exposure, complication – oroantral fistula
 Lateral rhinotomy approach with medial maxillectomy – if extends beyond nasopharynx into
 Sardana’s approach – transpalatine along with sublabial, extension to sublabial area
 Endoscopic approach – endonasal – for small and medium sized tumours
 Mid facial degloving approach – good cosmetic results
 Le fort’s type I osteotomy/ trans maxillary approach - extension to PNS,
pterygopalatine fossa
 Biller’s transmandibular lip splitting approach – infratemporal fossa, pterygoid muscles
 Craniotomy
 Other modalities
 RT – advanced disease, intracranial extension
 Complication – osteoradionecrosis, secondary malignancies, cataract, optic atrophy
 High recurrence with RT
 CT
 Very aggressive tumours
 Doxorubicin, Vincristine
 Prognosis
 Early diagnosis -> good prognosis
Nasopharyngeal Malignancies
 Carcinoma (mc)
 Non Hodgkin’s lymphoma
 Rhabdomyosarcoma
 Plasmocytoma
 Chordoma
 Adenoid cystic carcinoma
Nasopharyngeal Carcinoma
 Incidence – 2% of malignancies of head and neck
 Age group – Bimodal – 10 -20 years (more aggressive), 50 – 70 years
 M:F = 3:1
 MC in Chinese/ mongoloids – south china, Taiwan, Indonesia, Hong kong, Thailand, Malaysia, NE India
mainly Nagaland
 Etiology
 Enviromental factors – Air pollution, wood burning, incense sticks smoke, chemical fumes inhalation,
exposure to nickel, chromium, radioactive material, polycystic hydrocarbons, household smoke and fumes
 Dietary ingestion of nitrosamines in form of salted fish, smoked food, Chinese herbal medicine usage,
alcohol, smoking, tobacco, opium
 Vitamin C deficiency
 Genetic – chromosomal abnormalities
 EB Virus – increased antibody titres – in 90% especially undifferentiated/ poorly differentiated
cancers
 Pathology
 Proliferative type – Nasal obstruction
 Ulcerative type – epistaxis
 Infiltrative type – CN involved, invasive
 Histological classification
 Type I – well differentiated keratinizing scc – 25%
 Type II – differentiated non keratinizing – 12%
 Type III – undifferentiated/ anaplastic non keratinizing – 63%
 Type II and III – transitional cell carcinoma, lymphoepithelioma
 Spread
 MC site of origin – fossa of rosenmuller in lateral wall of nasopharynx
 Superiorly – intracranial cavity by destruction of basisphenoid and basiocciput
 Laterally – parapharyngeal space, infratemporal fossa
 Anteriorly – Nasal cavity, PNS, orbit
 Inferiorly – oropharynx, soft palate
 Lymphatic – early lymphatic spread, B/L involvement common in advance cases,
retropharyngeal and parapharyngeal lymph nodes to upper deep cervical and posterior
group of lymph nodes
 CN – VI (1st nerve involved), V, IX, X, XI, XII
 Haematogenous – Bone (Spine, shoulder, pelvis, skull), liver and lungs
 C/F
 Cervical – Lump in neck – 60-80%, 50% B/L –MC symptom
 Ear – Hearing loss (CHL) U/L due to SOM unresolving associated with otalgia, tinnitus, giddiness
due to ET blockage – 2nd MC symptom
 Nose – Nasal obstruction (u/l or b/l) associated with blood stained nasal discharge and foul smell
– 3rd MC symptom, rhinolalia clausa
 Epistaxis
 Eye – diplopia (VI CN), epiphora, proptosis, loss of corneal reflex, diminished vision
 CNS – headache (V CN), ophthalmoplegia (III,IV and VI CN), Neck and facial pain (V CN), jugular
foramen syndrome (IX, X, XI CN), exophthalmos and blindness (II CN), horner’s syndrome (cervical
sympathetic chain)
 Weight loss, loss of appetite
 L/E
 Pharyngeal – palatal swelling or soft palate bulge
 Post rhinoscopy – diffuse bulge or ulceroproliferative growth in nasopharynx
 Ant rhinoscopy – mass in nose, friable, bleeds on touch, blood stained discharge
 Trotter’s triad
 Conductive hearing loss (ET blockage), I/L temporo parietal/ mandibular pain – V
CN, Soft palate paralysis/ decreased mobility – X CN
 Trismus – pterygoid muscles
 Diagnosis
 Pan endoscopy – to rule out 2nd tumour
 DNE, PTA, Tympanogram
 Biopsy under vision
 FNAC
 CT Scan – HRCT Neck and Nasopharynx – toc
 MRI
 CT Lung, Abdomen, Chest X Ray
 USG abdomen
 Bone Scan
 Serology - EBV
 TNM Staging
 T1 – Nasopharynx
 T2a – Oropharynx, Nasal cavity without parapharyngeal spread
 T2b – With parapharyngeal spread
 T3 – Bony structures, PNS
 T4 – Intracranial, CN, infratemporal fossa
 N1 – I/L LN upto 6 cm
 N2 – C/L or B/L LN upto 6 cm
 N3a – Any LN > 6 cm
 N3b – Involves supraclavicular fossa
 Supraclavicular fossa / Ho’s triangle – clavicle medially and laterally, where neck meets the shoulder
 Staging
 I – T1
 II A – T2a
 II B – T2b or N1
 III – T3 or N2
 IV A – T4
 IV B – N3
 IV C – M1
Treatment
 RT - TOC
 External beam RT – 6000 - 7000 rads
 Main treatment
 Stage III and IV – RT and CT
 5 FU and cisplatin
 Residual/ recurrence
 RND
 2nd dose of external RT
 Brachytherapy
 Surgery
 Surgical approaches
 Fisch approach
 Biller’s approach
 Maxillary swing approach
 Nasopharyngectomy
 Prognosis
 Stage III and IV – RT more effective – good prognosis
 Early diagnosis – good prognosis
Tumours of Oropharynx
 Benign tumours
 Mucous retention cyst – Vallecula, yellowish – pedunculated or sessile smooth
cyst
 Most of the patients are asymptomatic with accidental finding on examination
 Few – foreign body sensation in throat
 Treatment
 If pedunculated – excision
 If cystic – marsipulization ( incision and drainage with removal of cyst wall)
 Papilloma – Seen over tonsils, soft palate, faucial pillars – pedunculated
 Asymptomatic or local irritation of throat
 Treatment – excision
 Pleomorphic adenoma – Hard palate, soft palate, treatment – excision
 Haemangioma – Palate, tonsil, post pharyngeal wall, congenital, females,
regresses after age of 2 years
 Dysphagia, bleeding
 If persists after 3 years – surgical resection, cryotherapy, coagulation by LASER,
diathermy
Malignancy of oropharynx
 Etiology
 Common in South Asia, Males, age group 50 – 70 years
 Alcohol
 Smoking
 Betelnut chewing
 Poor orodental hygiene
 Atmospheric pollution
 HPV 16 – SCC Tonsil
 Types
 SCC – 90%
 Lymphoma – 20% (Tonsils) – Non Hodgkin’s lymphoma
 Minor salivary gland tumours – soft palate, hard palate, pillars –
ca, adenoid cystic ca
 Sites
 Lateral wall – MC – Tonsils 50%
 Base of tongue & Vallecula – 2nd MC – 40%
 Post pharyngeal wall – 10%
 C/F
 Associated with lymph node swelling
 Early symptoms
 Neck swelling, throat irritation, burning sensation with acidic food, lump in throat
 Late symptoms
 Dysphagia, odynophagia, dysarthria, hot potato voice, trismus
 Other symptoms
 Unilateral referred otalgia, ulcer in throat, increase salivation, drooling of saliva,
muffled speech, neck pain, oral bleed, hemoptysis
 Signs
 Ulcerative lesion/ endophytic lesion – base of tongue, vallecula
 Exophytic/ Proliferative lesion – tonsillar fossa, soft palate, post pharyngeal wall
 IDL examination – base of tongue, vallecula, tonsillo lingual sulcus
 Digital palpation
 Post rhinoscopy – nasopharyngeal surface of soft palate
 Tongue movements restricted, deviation of tongue
 Lymph node enlargement – I, II, III. IV, V, base of tongue lesions (70%) can be B/L
mainly JD LN, Post pharyngeal wall 60% can be B/L, Tonsils 50% mainly JD, Faucial
– LN Ib, II
 Distant Metastasis
 Bone, liver, lung
 TNM Staging
 T staging
 Tx , Tis
 T1 – upto 2 cm, T2 - > 2 upto 4cm, T3 - > 4 cm
 T4a – involves surrounding structures – muscles of tongue, larynx, hard palate, mandible, medial
pterygoids
 T4b – involves lateral pterygoids, nasopharynx, skull base, carotid
 N
 M
 Stage I – T1, Stage II – T2, Stage III – T3 or N1, Stage IV a – T4a or N2, Stage IV b – T4b or N3,
Stage IV c – M1
 Diagnosis
 Biopsy – punch biopsy , under GA if trismus, hidden areas
 Excisional biopsy – lymphomas (tonsillectomy)
 Pan endoscopy – secondary primary
 FNAC – LN
 USG Neck – LN
 X Ray Mandible/ OPG
 Chest X Ray
 CT Scan with contrast, MRI, PET Scan
 D/D – Tuberculosis ulcer, syphilis, Vincent’s angina. Quinsy
 Treatment
 Surgery – local excision and neck dissection
 RT
 CT
 Combined
 Palliative – advanced tumours – pain relief, tracheostomy, gastrostomy
 Prognosis – poor as late presentation
 Early stage – RT, organ preservation, laser excision
 If N0 – Selective neck dissection, N1 – RND
 Advanced stage – surgical resection along with mandibulectomy along with RND
(COMMANDO operation) followed by post operative RT
 Concurrent CT RT
 Tonsillar fossa
 B/L Neck dissection may be required
 Lymphomas
 B cell high grade Non Hodgkin’s lymphoma
 M:F 2:1, children and young adults
 Site – tonsil (mc), base of tongue
 EBV associated with it
 Smooth bulky mass, U/L swelling of tonsil
 Treatment – RT, RT and CT
Tumours of Hypopharynx
 Benign tumours
 Lipoma (mc), papilloma, adenoma, fibroma, leiomyoma
 Malignant tumours
 SCC 95%
 Lymphomas – AIDS
 Sarcoma
 Sites – Pyriform sinus (60%)
 Post cricoid (30%)
 Post pharyngeal wall (10%)
 Etiology
 Alcohol (mc)
 Smoking
 Genetic
 Radiation
 Plummer vinson syndrome/ Patterson brown Kelly syndrome/ sideropenic
anaemia – hypochromic microcytic iron deficiency anaemia – POST CRICOID
 Low socio economic status
 Age group > 50 yrs, male – commonest cause of dysphagia in elderly male
 Post cricoid – females, 20 – 40 yrs age
 Pathology
 Proloferative/ exophytic/ cauliflower like – post pharyngeal wall
 Ulcerative/ endophytic
 Ulceroproliferative
 Microscopy
 Well differentiated (mc), moderately differentiated, poorly differentiated, anaplastic
 Spread – lymphatic, direct, hematogenous
 Lymphatic spread
 Pyriform sinus – 75% chance of lymph node spread, 30% B/L, LEVEL II and III
 Post cricoid – 20% chance of lymph node spread, B/L common, paratracheal
lymph node, IV, VI, VII
 Post pharyngeal wall – 40% chance of lymph node spread, RP LN (mc), IV
 Hematogenous – lung, liver, bone
 Direct – paraglottic space leading to fixation of vc, supraglottis, oropharynx,
cricopharyngeal sphincter, laryngeal cartilages, thyroid gland
 C/F
 Progressive dysphagia more to solids for more than 1 month. Dysphagia is a late symptom but early in
post cricoid malignancy
 Neck swelling
 Sticking of food in throat, lump in throat (1st symptom), FB sensation in throat, pricking sensation in
throat
 Hoarseness
 Stridor
 Choking spells, shortness of breath, aspiration
 Referred otalgia
 Spitting of blood
 Odynophagia/ pain in neck – late symptom
 Signs
 IDL
 Ulcerative/ proliferative growth
 Pooling of saliva – post cricoid malignancy
 Fixed VC
 Oedema/ erythema of arytenoids/ post cricoid area – post cricoid malignancy
 Neck – LN metastasis
 Widening and splaying of larynx
 Larynx pushed forwards – post cricoid malignancy
 Laryngeal crepitus absent – post cricoid malignancy
 Diagnosis
 X Ray Neck – AP/Lat – cartilage erosion, pre vertebral widening, airway patency
 Chest X ray – mediastinal widening, aspiration pneumonia, secondaries
 Barium swallow with fluoroscopy – oesophagus, upper esophageal sphincter
 FNAC
 DL Scopy/ hypopharyngoscopy and biopsy
 CECT – primary modality, cartilage invasion
 PET – recurrent, residual disease, distant metastasis
 MRI
 TNM Staging
 T1 – limited to one site of hypopharynx and upto 2 cm
 T2 – Greater than 1 site or > 2 cm without fixation of larynx
 T3 – Greater than 4 cm with fixation of larynx
 T4a – involves thyroid, cricoid cartilage, thyroid gland, oesophagus, supraglottis,
cricopharyngeal sphincter
 T4b – involves prevertebral, carotid, mediastinum
 N
 M
 STAGING
 Treatment
 Early stage – RT
 Advanced stage – Surgery and post op RT
 CT – adjuvant/ palliative
 Surgery –
 Early stage – laser excision, partial pharyngectomy, partial laryngopharyngectomy
 Late stage – total laryngo pharyngo esophagectomy with gastric pull up/ colonic transposition
 Reconstruction – PMMC flap, free flaps – radial forearm, lateral thigh, enteric flaps – jejunal ,
omental
 Neck dissection – selective (N0), RND
 Prognosis
 Early diagnosis – rare - good prognosis – 80% 5 year survival
 Late diagnosis – poor prognosis – 30% 5 year survival
 Post cricoid malignancy – poor prognosis – early B/L LN metastasis, vertebral
column spread

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Tumours of pharynx

  • 2. Tumours of Nasopharynx  BENIGN TUMOURS  Juvenile Nasopharyngeal Angiofibroma (mc)  Craniopharyngioma  Rhabdomyoma  Teratoma, Paraganglioma  Chondroma, Chordoma  Hamartoma, Haemangioma  Pleomorphic adenoma, Warthin’s tumour
  • 3. Juvenile Nasopharyngeal Angiofibroma  Histologically benign but locally aggressive vascular tumour occupying nasopharynx seen in adolescent males causing recurrent unprovoked episodes of epistaxis  Incidence 0.05 to 0.1% of head & neck cancers  Etiology  Age gp – 10 – 25 years of age, adolescents (mc), regresses/ stops growing after 25 yrs of age  Sex – males (exclusive)  Nasal erectile vascular tissue(hamartomatous nidus of inf turbinate tissue) mislocated in nasopharynx -> gets activated when testosterone acts on it -> NPA  Abnormal growth of nasopharyngeal fibrocartilage/ fibrovascular stroma  Origin from non chromaffin preganglionic cells of terminal branches of maxillary artery
  • 4.  Genetic/ Heredity  Trauma  Infection  Allergy  Pathology  Contains both vascular and fibrous tissue  Covered with nasopharyngeal mucosa – deceives vascularity  Pink grey or purple red colour, sessile or pedunculated  No capsule – invades locally  Thin walled vessels just endothelial lined, no muscular coat – bleeding which cant be controlled by adrenaline
  • 5.  Extension  Origin – above sup margin of sphenopalatine foramen in lat wall of nasopharynx, attached to roof of choana, post part of middle turbinate, post part of nasal septum  Locally invasive  Anteriorly – nasal cavity, orbit  Posteriorly – destroys pterygoid plates, extends to vidian nerve  Superiorly – sphenoid sinus->cavernous sinus, middle cranial fossa  Sphenoid sinus -> post ethmoids, ant cranial fossa  Laterally -> pterygopalatine fossa -> maxillary sinus -> infratemporal fossa -> cheek
  • 6.  Clinical features  Nasal  U/L gradually increasing nasal obstruction, later B/L  Recurrent painless unprovoked episodes of nasal bleed  Nasal discharge  Loss of smell  Mouth breathing/ snoring  Rhinolalia clausa  Ear  Blockage in ear due to ET blockage leading to serous otitis media and conductive hearing loss, otalgia, tinnitus
  • 7.  Eyes  Pain, proptosis, lacrimation, diplopia, rarely blindness  Face  Cheek swelling, broadening of nasal bridge, frog face deformity  CNS  II CN – blindness  III, IV, VI CN – diplopia  V CN – neuralgic pain  Increased intracranial pressure – headache, blurring of vision, projectile vomiting  General – Anaemia, sexual underdevelopment  NO LYMPH NODE INVOLVEMENT
  • 8.  Signs  Post rhinoscopy  Pink, purple, reddish globular sessile lobulated mass, firm in consistency obstructing one or both choana, may be visible below nasopharyngeal isthmus  Ant rhinoscopy  Globular pinkish mass in post part of nasal cavity, septum deviated to opposite side  NO PROBE TEST, NO DIGITAL PALPATION  Oral cavity – soft palate bulge  D/D – Infected AC polyp, carcinoma, rhinosporodiosis, craniopharyngioma
  • 9.  Diagnosis  Clinical  DNE  Biopsy – Only excision biopsy  Radiology  X ray soft tissue nasopharynx lateral view – soft tissue in NP  CT Scan with contrast – gold standard  Vascular dumb bell shaped tumour in nasal cavity, nasopharynx, pterygopalatine foramen  Anterior bowing of posterior wall of maxillary sinus and post bowing of pterygoids – Holman Miller sign/ Antral sign  MRI – intracranial/ orbit extension
  • 10.  Digital Subtraction Angiography (DSA)/ Carotid angiography  Tumour can be seen  Also used to embolise feeding vessel on same side – internal maxillary artery  Materials used – gelfoam, PVA  Helps to reduce bleeding intraoperatively  Operate 24- 48 hours after embolization  Always arrange blood transfusion before surgery  Other methods to reduce bleeding – estrogen therapy, pre op RT, cryotherapy
  • 11.  Staging Sessions/ Fisch ()  I A – limited to nasopharynx and nose (I)  I B – Extend to PNS (II)  II A – Minimal extension to pterygomaxillary fossa (II)  II B – Full occupation of pterygomaxillary fossa with bony erosion of orbit (II)  III A – Erosion of skull base with minimal intracranial extension (III)  III B – Extensive intracranial extension with extending to cavernous sinus, optic chiasma, pituitary fossa (IV)
  • 12.  Treatment  Surgical excision – TOC  Complete excision  Approaches  Wilson’s transpalatal approach – Preferred if tumour limited to nose and nasopharynx – U incision made at the junction of soft and hard palate – separation of hard and soft palate – part hard palate removed for better exposure, complication – oroantral fistula  Lateral rhinotomy approach with medial maxillectomy – if extends beyond nasopharynx into  Sardana’s approach – transpalatine along with sublabial, extension to sublabial area  Endoscopic approach – endonasal – for small and medium sized tumours
  • 13.  Mid facial degloving approach – good cosmetic results  Le fort’s type I osteotomy/ trans maxillary approach - extension to PNS, pterygopalatine fossa  Biller’s transmandibular lip splitting approach – infratemporal fossa, pterygoid muscles  Craniotomy  Other modalities  RT – advanced disease, intracranial extension  Complication – osteoradionecrosis, secondary malignancies, cataract, optic atrophy  High recurrence with RT
  • 14.  CT  Very aggressive tumours  Doxorubicin, Vincristine  Prognosis  Early diagnosis -> good prognosis
  • 15. Nasopharyngeal Malignancies  Carcinoma (mc)  Non Hodgkin’s lymphoma  Rhabdomyosarcoma  Plasmocytoma  Chordoma  Adenoid cystic carcinoma
  • 16. Nasopharyngeal Carcinoma  Incidence – 2% of malignancies of head and neck  Age group – Bimodal – 10 -20 years (more aggressive), 50 – 70 years  M:F = 3:1  MC in Chinese/ mongoloids – south china, Taiwan, Indonesia, Hong kong, Thailand, Malaysia, NE India mainly Nagaland  Etiology  Enviromental factors – Air pollution, wood burning, incense sticks smoke, chemical fumes inhalation, exposure to nickel, chromium, radioactive material, polycystic hydrocarbons, household smoke and fumes  Dietary ingestion of nitrosamines in form of salted fish, smoked food, Chinese herbal medicine usage, alcohol, smoking, tobacco, opium  Vitamin C deficiency  Genetic – chromosomal abnormalities
  • 17.  EB Virus – increased antibody titres – in 90% especially undifferentiated/ poorly differentiated cancers  Pathology  Proliferative type – Nasal obstruction  Ulcerative type – epistaxis  Infiltrative type – CN involved, invasive  Histological classification  Type I – well differentiated keratinizing scc – 25%  Type II – differentiated non keratinizing – 12%  Type III – undifferentiated/ anaplastic non keratinizing – 63%  Type II and III – transitional cell carcinoma, lymphoepithelioma
  • 18.  Spread  MC site of origin – fossa of rosenmuller in lateral wall of nasopharynx  Superiorly – intracranial cavity by destruction of basisphenoid and basiocciput  Laterally – parapharyngeal space, infratemporal fossa  Anteriorly – Nasal cavity, PNS, orbit  Inferiorly – oropharynx, soft palate  Lymphatic – early lymphatic spread, B/L involvement common in advance cases, retropharyngeal and parapharyngeal lymph nodes to upper deep cervical and posterior group of lymph nodes  CN – VI (1st nerve involved), V, IX, X, XI, XII  Haematogenous – Bone (Spine, shoulder, pelvis, skull), liver and lungs
  • 19.  C/F  Cervical – Lump in neck – 60-80%, 50% B/L –MC symptom  Ear – Hearing loss (CHL) U/L due to SOM unresolving associated with otalgia, tinnitus, giddiness due to ET blockage – 2nd MC symptom  Nose – Nasal obstruction (u/l or b/l) associated with blood stained nasal discharge and foul smell – 3rd MC symptom, rhinolalia clausa  Epistaxis  Eye – diplopia (VI CN), epiphora, proptosis, loss of corneal reflex, diminished vision  CNS – headache (V CN), ophthalmoplegia (III,IV and VI CN), Neck and facial pain (V CN), jugular foramen syndrome (IX, X, XI CN), exophthalmos and blindness (II CN), horner’s syndrome (cervical sympathetic chain)  Weight loss, loss of appetite
  • 20.  L/E  Pharyngeal – palatal swelling or soft palate bulge  Post rhinoscopy – diffuse bulge or ulceroproliferative growth in nasopharynx  Ant rhinoscopy – mass in nose, friable, bleeds on touch, blood stained discharge  Trotter’s triad  Conductive hearing loss (ET blockage), I/L temporo parietal/ mandibular pain – V CN, Soft palate paralysis/ decreased mobility – X CN  Trismus – pterygoid muscles
  • 21.  Diagnosis  Pan endoscopy – to rule out 2nd tumour  DNE, PTA, Tympanogram  Biopsy under vision  FNAC  CT Scan – HRCT Neck and Nasopharynx – toc  MRI  CT Lung, Abdomen, Chest X Ray  USG abdomen  Bone Scan  Serology - EBV
  • 22.  TNM Staging  T1 – Nasopharynx  T2a – Oropharynx, Nasal cavity without parapharyngeal spread  T2b – With parapharyngeal spread  T3 – Bony structures, PNS  T4 – Intracranial, CN, infratemporal fossa  N1 – I/L LN upto 6 cm  N2 – C/L or B/L LN upto 6 cm  N3a – Any LN > 6 cm  N3b – Involves supraclavicular fossa  Supraclavicular fossa / Ho’s triangle – clavicle medially and laterally, where neck meets the shoulder
  • 23.  Staging  I – T1  II A – T2a  II B – T2b or N1  III – T3 or N2  IV A – T4  IV B – N3  IV C – M1
  • 24. Treatment  RT - TOC  External beam RT – 6000 - 7000 rads  Main treatment  Stage III and IV – RT and CT  5 FU and cisplatin  Residual/ recurrence  RND  2nd dose of external RT  Brachytherapy  Surgery
  • 25.  Surgical approaches  Fisch approach  Biller’s approach  Maxillary swing approach  Nasopharyngectomy  Prognosis  Stage III and IV – RT more effective – good prognosis  Early diagnosis – good prognosis
  • 26. Tumours of Oropharynx  Benign tumours  Mucous retention cyst – Vallecula, yellowish – pedunculated or sessile smooth cyst  Most of the patients are asymptomatic with accidental finding on examination  Few – foreign body sensation in throat  Treatment  If pedunculated – excision  If cystic – marsipulization ( incision and drainage with removal of cyst wall)
  • 27.  Papilloma – Seen over tonsils, soft palate, faucial pillars – pedunculated  Asymptomatic or local irritation of throat  Treatment – excision  Pleomorphic adenoma – Hard palate, soft palate, treatment – excision  Haemangioma – Palate, tonsil, post pharyngeal wall, congenital, females, regresses after age of 2 years  Dysphagia, bleeding  If persists after 3 years – surgical resection, cryotherapy, coagulation by LASER, diathermy
  • 28. Malignancy of oropharynx  Etiology  Common in South Asia, Males, age group 50 – 70 years  Alcohol  Smoking  Betelnut chewing  Poor orodental hygiene  Atmospheric pollution  HPV 16 – SCC Tonsil
  • 29.  Types  SCC – 90%  Lymphoma – 20% (Tonsils) – Non Hodgkin’s lymphoma  Minor salivary gland tumours – soft palate, hard palate, pillars – ca, adenoid cystic ca  Sites  Lateral wall – MC – Tonsils 50%  Base of tongue & Vallecula – 2nd MC – 40%  Post pharyngeal wall – 10%
  • 30.  C/F  Associated with lymph node swelling  Early symptoms  Neck swelling, throat irritation, burning sensation with acidic food, lump in throat  Late symptoms  Dysphagia, odynophagia, dysarthria, hot potato voice, trismus  Other symptoms  Unilateral referred otalgia, ulcer in throat, increase salivation, drooling of saliva, muffled speech, neck pain, oral bleed, hemoptysis
  • 31.  Signs  Ulcerative lesion/ endophytic lesion – base of tongue, vallecula  Exophytic/ Proliferative lesion – tonsillar fossa, soft palate, post pharyngeal wall  IDL examination – base of tongue, vallecula, tonsillo lingual sulcus  Digital palpation  Post rhinoscopy – nasopharyngeal surface of soft palate  Tongue movements restricted, deviation of tongue  Lymph node enlargement – I, II, III. IV, V, base of tongue lesions (70%) can be B/L mainly JD LN, Post pharyngeal wall 60% can be B/L, Tonsils 50% mainly JD, Faucial – LN Ib, II
  • 32.  Distant Metastasis  Bone, liver, lung  TNM Staging  T staging  Tx , Tis  T1 – upto 2 cm, T2 - > 2 upto 4cm, T3 - > 4 cm  T4a – involves surrounding structures – muscles of tongue, larynx, hard palate, mandible, medial pterygoids  T4b – involves lateral pterygoids, nasopharynx, skull base, carotid  N  M
  • 33.  Stage I – T1, Stage II – T2, Stage III – T3 or N1, Stage IV a – T4a or N2, Stage IV b – T4b or N3, Stage IV c – M1  Diagnosis  Biopsy – punch biopsy , under GA if trismus, hidden areas  Excisional biopsy – lymphomas (tonsillectomy)  Pan endoscopy – secondary primary  FNAC – LN  USG Neck – LN  X Ray Mandible/ OPG  Chest X Ray  CT Scan with contrast, MRI, PET Scan
  • 34.  D/D – Tuberculosis ulcer, syphilis, Vincent’s angina. Quinsy  Treatment  Surgery – local excision and neck dissection  RT  CT  Combined  Palliative – advanced tumours – pain relief, tracheostomy, gastrostomy  Prognosis – poor as late presentation
  • 35.  Early stage – RT, organ preservation, laser excision  If N0 – Selective neck dissection, N1 – RND  Advanced stage – surgical resection along with mandibulectomy along with RND (COMMANDO operation) followed by post operative RT  Concurrent CT RT  Tonsillar fossa  B/L Neck dissection may be required
  • 36.  Lymphomas  B cell high grade Non Hodgkin’s lymphoma  M:F 2:1, children and young adults  Site – tonsil (mc), base of tongue  EBV associated with it  Smooth bulky mass, U/L swelling of tonsil  Treatment – RT, RT and CT
  • 37. Tumours of Hypopharynx  Benign tumours  Lipoma (mc), papilloma, adenoma, fibroma, leiomyoma  Malignant tumours  SCC 95%  Lymphomas – AIDS  Sarcoma  Sites – Pyriform sinus (60%)  Post cricoid (30%)  Post pharyngeal wall (10%)
  • 38.  Etiology  Alcohol (mc)  Smoking  Genetic  Radiation  Plummer vinson syndrome/ Patterson brown Kelly syndrome/ sideropenic anaemia – hypochromic microcytic iron deficiency anaemia – POST CRICOID  Low socio economic status
  • 39.  Age group > 50 yrs, male – commonest cause of dysphagia in elderly male  Post cricoid – females, 20 – 40 yrs age  Pathology  Proloferative/ exophytic/ cauliflower like – post pharyngeal wall  Ulcerative/ endophytic  Ulceroproliferative  Microscopy  Well differentiated (mc), moderately differentiated, poorly differentiated, anaplastic  Spread – lymphatic, direct, hematogenous
  • 40.  Lymphatic spread  Pyriform sinus – 75% chance of lymph node spread, 30% B/L, LEVEL II and III  Post cricoid – 20% chance of lymph node spread, B/L common, paratracheal lymph node, IV, VI, VII  Post pharyngeal wall – 40% chance of lymph node spread, RP LN (mc), IV  Hematogenous – lung, liver, bone  Direct – paraglottic space leading to fixation of vc, supraglottis, oropharynx, cricopharyngeal sphincter, laryngeal cartilages, thyroid gland
  • 41.  C/F  Progressive dysphagia more to solids for more than 1 month. Dysphagia is a late symptom but early in post cricoid malignancy  Neck swelling  Sticking of food in throat, lump in throat (1st symptom), FB sensation in throat, pricking sensation in throat  Hoarseness  Stridor  Choking spells, shortness of breath, aspiration  Referred otalgia  Spitting of blood  Odynophagia/ pain in neck – late symptom
  • 42.  Signs  IDL  Ulcerative/ proliferative growth  Pooling of saliva – post cricoid malignancy  Fixed VC  Oedema/ erythema of arytenoids/ post cricoid area – post cricoid malignancy  Neck – LN metastasis  Widening and splaying of larynx  Larynx pushed forwards – post cricoid malignancy  Laryngeal crepitus absent – post cricoid malignancy
  • 43.  Diagnosis  X Ray Neck – AP/Lat – cartilage erosion, pre vertebral widening, airway patency  Chest X ray – mediastinal widening, aspiration pneumonia, secondaries  Barium swallow with fluoroscopy – oesophagus, upper esophageal sphincter  FNAC  DL Scopy/ hypopharyngoscopy and biopsy  CECT – primary modality, cartilage invasion  PET – recurrent, residual disease, distant metastasis  MRI
  • 44.  TNM Staging  T1 – limited to one site of hypopharynx and upto 2 cm  T2 – Greater than 1 site or > 2 cm without fixation of larynx  T3 – Greater than 4 cm with fixation of larynx  T4a – involves thyroid, cricoid cartilage, thyroid gland, oesophagus, supraglottis, cricopharyngeal sphincter  T4b – involves prevertebral, carotid, mediastinum  N  M  STAGING
  • 45.  Treatment  Early stage – RT  Advanced stage – Surgery and post op RT  CT – adjuvant/ palliative  Surgery –  Early stage – laser excision, partial pharyngectomy, partial laryngopharyngectomy  Late stage – total laryngo pharyngo esophagectomy with gastric pull up/ colonic transposition  Reconstruction – PMMC flap, free flaps – radial forearm, lateral thigh, enteric flaps – jejunal , omental  Neck dissection – selective (N0), RND
  • 46.  Prognosis  Early diagnosis – rare - good prognosis – 80% 5 year survival  Late diagnosis – poor prognosis – 30% 5 year survival  Post cricoid malignancy – poor prognosis – early B/L LN metastasis, vertebral column spread