trans 44 and 45 tumors of the head and neck Flashcards

1
Q

primary etiologic agent in the

pathogenesis of nasopharyngeal carcinoma.

A

EBV

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2
Q

rule of 80s in salivary gland neoplasm

A

Rule of 80’s
o 80% of parotid tumors are benign
o 80% of parotid tumors are Pleomorphic adenomas
o 80%ofsalivaryglandPleomorphicadenomasoccurinthe
parotid
o 80% of Pleomorphic adenomas occur in the superficial
lobe
o 80% of untreated Pleomorphic adenomas remain benign

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3
Q

histology of what?

Mixture of epithelial, myoepithelial and stromal components • Epithelial cells: nests, sheets, ducts, trabeculae
• Stroma: myxoid, chondroid, fibroid, osteoid
• No true capsule
• Solid
• Cystic changes • Myxoid stroma
Figure 1. Pleomorphic Adenoma
II. TUMORS OF THE HEAD AND NECK
A. SALIVARY GLAND NEOPLASMS
• Tumor pseudopods  False feet

A

pleomorphic adenoma

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4
Q
aka Papillary cystadenoma lymphomatosum
• 6-10% of parotid neoplasms
• Older, Caucasian, Males
• 10% bilateral or multicentric
• 3% with associated neoplasms
 The key here is there is a cystic and lymphoid component in
the tumor
A

warthin’s tumor

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5
Q
Most common salivary gland malignancy
• 5-9% of salivary neoplasms
• Parotid 45-70% of cases
• Palate 18%
• 3rd-8th decades, peak in the 5th decade
• F>M
• Caucasians > African American
A

MUCOEPIDERMOID CARCINOMA

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6
Q
Overall 2nd most common malignancy
• Most common in submandibular, sublingual and minor
salivary glands
• M=F
• 5th decade
A

ADENOID CYSTIC CARCINOMA

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7
Q

Cribriform pattern
o Mostcommon
o “swisscheese”appearance

A

ADENOID CYSTIC CARCINOMA

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8
Q

2nd most common parotid and pediatric malignancy
• 5th decade
• F>M
• Bilateral parotid disease in 3%

A

Acinic Cell Carcinoma

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9
Q

sistrunk procedure?

A

The Sistrunk procedure consists of removing a thyroglossal duct cyst and surrounding tissues.

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10
Q

Congenital, remnants of thyroglossal tract
• Mostly infrahyoid
• Can appear at any age (mostly 15-30)
• Painless lump in the midline of the neck
• Pain and redness if infected (fistula)
• Spherical, smooth, mobile cyst in the midline
• Moves with swallowing and tongue protrusion
• Required surgery (Sistrunk procedure)

A

Thyroglossal Duct Cyst

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11
Q
  • Cystic mass behind the anterior margin of the SCM
  • Remnant of 2nd Branchial clefts
  • Appear at any age (mostly 15-25)
  • Painless swelling
  • Hard, smooth, not very mobile
  • Full of yellowish golden material, cholesterol crystals
  • Cannot be reduced or compressed
  • May have small sinus tract into tonsillar fossae
A

Branchial Cleft Cyst

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12
Q

Cyst swelling floor of mouth (ranula = little frog)
• Mucus extravasations from sublingual salivary gland
• May extend through FOM muscles into neck

A

Ranula

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13
Q

Collection of lymphatic sacs which contain clear colorless lymph
• Congenital
• Present at birth or within the first years of life
• Commonly found at the base of the neck, occupying large
space
• Lobulated and flattened cysts
• Smooth and very close to skin and contain clear fluid →
Transillumination

A

CYSTIC HYGROMA (LYMPHANGIOMA)

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14
Q

Purplish mass typical for diagnosis
• Can be found at any place in the body

The most common benign tumor of the body in children • Treatment
o Surgery/laser/Steroids/Beta blockers
 Nowadays, they found out that the most effective
treatment are the Beta blockers

A

HEMANGIOMA

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15
Q

Rare tumor of the chemoreceptor tissue of the carotid body (Chemodectoma)
• 40-60 years of age
• Painless slowly growing pulsating lump
• Upper part of the ant triangle
• Solid, hard, pulsating spherical or irregular mass
• Can move from side to side but not up and down

A

Carotid Body Tumor

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16
Q

Most common is lymphoma (Hodgkin’s and non-Hodgkin’s) • Common in children and young adults
• Symptoms:
o Painless slowly growing neck lump, malaise, weight loss, pallor, pruritus, fever, night sweat

A

PRIMARY LYMPH NODE NEOPLASM

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17
Q

Enlarged lymph node

Asymmetric
• Adults
• Fixed “immobile”
• Hard
• Non-tender initially
• Look for primary tumor
A

METASTATIC LYMPH NODES

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18
Q

Benign lesion derived from follicular epithelium
• Usually single, well encapsulated
• Discrete lesions with grandular/acinar follicular pattern
• Papillary change is not typical but if + suggest Papillary Ca

A

THYROID ADENOMA

19
Q

Most common type of thyroid ca – 60 to 80%
• Female: Male: 2:1
• Mean age at presentation – 35 yrs
• More common in persons exposed to radiation
• Macroscopic – Hard, whitish, calcified, unencapsulated • Microscopic features:

  1. Cuboidal cells with abundant cytoplasm
  2. Intranuclear cytoplasmic inclusions
  3. Orphan Annie cell
  4. Fibrovascular stroma with calcium
    “psammona bodies
A

PAPILLARY THYROID CARCINOMA

20
Q

PAPILLARY THYROID CARCINOMA – 7PS

A
  • Popular – most common thyroid CA
  • Psammoma bodies
  • Palpable lymph nodes (seen in 33% of patients)
  • Positive 131 I(iodine) uptake
  • Positive prognosis
  • Postoperative 131 I(iodine) scan to diagnose/treat metastasis
  • Pulmonary metastases
21
Q
  • Female: Male: 3:1
  • Accounts for 30 to 50% of all thyroid Ca
  • Mean age at presentation – 50 yrs
  • More frequent in iodine deficient areas
  • History of long standing goiter
A
  1. FOLLICULAR THYROID CARCINOMA
22
Q

FOLLICULAR THYROID CARCINOMA 4FS

A

Far-away metastasis – hematogenous spread
• Female (3:1)
• FNA…. Can’t diagnose this CA
• Favorable prognosis

23
Q

• Type of follicular cell carcinoma
• Derived from “Oxyphil cell” of thyroid.
• Function of these cells is not known
• Cells are stuffed with mitochondria & possess the TSH
receptors and produce thyroglobulin
• Compared to follicular type -usually multifocal & bilateral and
more likely to metastasize to lymph nodes  25%

A

HURTHLE CELL TUMOR

24
Q

• Female: Male: 1.5: 1
• Accounts for 1 to 2 % of all thyroid cancers
• Mean age at presentation – 50 to 60 yrs
• Sporadic -  75% cases, usually unilateral
• Familial -  25% cases, usually bilateral
o MutationinRETproto-oncogeneinchromosome10 o AspartofmultipleendocrineneoplasiatypeIIa
o As part of multiple endocrine neoplasia type IIb

A

medullary thyroid carcinoma

25
Q

Usually occurs in upper poles
• Originates from Parafollicular/ C cells
• Microscopic – why called Medullary
• Sheets of spindle shaped neoplastic cells with AMYLOID
(Altered Calcitonin) in between
• Cells stains for Calcitonin, CEA, Serotonin, VIP
• Spreads via lymphatics to cervical nodes

A

Medullary Thyroid Carcinoma

26
Q

Accounts for 2% of all thyroid cancers
• Female: Male: 1.5:1
• Mean age at presentation - 70 to 80 yrs
• Most Aggressive thyroid malignancy, with median survival
only  3 months
• Iodine deficiency goiter is precursor
• All patients are considered to have stage IV disease

A

ANAPLASTIC THYROID CARCINOMA

27
Q

• Accounts for  1 % of all thyroid Ca
• Women >70 yrs are usually affected
• In 70 to 80%, it arises in preexisting chronic lymphocytic
thyroiditis with subclinical or overt hypothyroidism, in
association with Hashimoto’s thyroiditis
• Almost always Non-Hodgkin B-cell Lymphoma
• Usually presents as rapidly growing mass, with obstructive
symptoms as dyspnea and dysphagia

A

THYROID LYMPHOMA

28
Q

• It is a benigh tumor of nasopharynx
• Exact etiology is not known
• It is a rare tumor
• Most commonly patient present with recurrent epistaxis or
profuse epistaxis
• Seen in adolescent males in 2nd decade of life (most
commonly at age 14 year with range 7-19 years)
• Its growth is thought to be testosterone dependent
o Origin of tumor: it is believed to arise from the posterior part of nasal cavity close to the superior margin of sphenopalatine foramen

A

JUVENILE NASOPHARYNGEAL ANGIOFIBROMA (JNA)

29
Q
  • Common in China particularly in southern states and Taiwan • Incidence of NPCA in China is 30-50/100,000 population
  • Sex: male: female = 2-3:1
  • Age: in Chinese risk start by 15-19 years of age
  • Average age group is 25-64 yrs
A

NASOPHARYNGEAL CARCINOMA (NPCA)

30
Q

Difference in gross appearance of proliferative, ulcerative, infiltrative nasopharyngeal carcinoma

A

Proliferative – When a polypoid tumour fills the nasopharynx, it causes obstructive nasal symptoms
Ulcerative – Epistaxis is the common symptom

Infiltrative – Growth infiltrate submucosally

31
Q

Treatment of choice for nasophangraeal carcinoma

A

Radiotherapy:
o treatment of choice, megavoltage radiation of 6000-
7000 rads

32
Q

Represent less than 5 % of all sinonasal tumors.
• Affects most commonly 5th -8th decade and rare before 40
years
• Usually unilateral.
• Association with HPV 6 & 11
• Symptoms: airway obstruction, epistaxis, asymptomatic
mass and pain

A

SCHNEIDERIAN PAPILLOMA (SINONASAL PAPILLOMA)

33
Q

• •
Arise in inflammatory conditions of nasal mucosa (Rhinosinusitis), disorders of ciliary motility or abnormal composition of nasal mucus

what polyp?

A

BILATERAL ETHMOIDAL POLYPS

34
Q

sampter’s triad?

A

nasal polyps, asthma and aspirin intolerance.

35
Q

kartagener syndrome

A

Bronchiectasis sinusitis, situs

inversus and ciliary dyskinesis.

36
Q

young syndrome

A

Sinopulmonary disease and

azoospermia.

37
Q

Churg-Strauss syndrome

A

Asthma, fever, eosinophilia, vasculitis and granuloma.

38
Q

This polyp arises from the mucosa of maxillary antrum near its accessory ostium, comes out of it and grows in the choana and nasal cavity.

A

D. ANTROCHOANAL POLYP (KILLIAN’S POLYP)

39
Q

Malignant neuroectodermal neoplasm arising from olfactory membrane of sinonasal tract.
• Olfactory placode tumor, esthesioneuroblastoma, esthesioneuroepithelioma.
 Another name
• Uncommon -2% SNT tumors
• Wide age ranges from 3 years to 9th decade
• Radiographically opacification of SNT with calcification
(speckled pattern)

A

D. OLFACTORY NEUROBLASTOMA

40
Q

site of olfactory neuroblatoma?

what are the clinical signs?

A

cribriform plate;

clinical signs:
anosmia
headache
nasal obstruction

41
Q

location of benign nodules in the larynx is where?

A

anterior 1/3

42
Q

Wart-like lesions in respiratory tract, causing recurrent obstruction.
• Young patients with stridor

A

recurrent papillomatosis

43
Q

• Mostly affects male above
• 40 years of age
• Growth is either exophytic, ulcerative and deeply infiltrative
• Because of large size of pyriform sinus growth of this region
remain asymptomatic for long time
• Metastatic neck nodes is the most common presenting
symptom

A

CARCINOMA PYRIFORM SINUS