Head and neck masses - evaluation and management Flashcards

1
Q

Anatomical considerations

A

Prominent landmarks
Triangles of the neck
Carotid bulb
Lymphatic levels

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2
Q

Common neck masses

A

Neoplastic
Congenital/ developmental
Inflammatory

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3
Q

General considerations: pt age

A
Paediatric (0-15 years): 90% benign
Young adult (16-40 yrs): similar to pediatric
Late adult (>40 years): "rule of 80s"
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4
Q

General considerations: location

A

Congenital masses: consistent in location

Metastatic masses: key to primary lesions

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5
Q

History

A

Developmental time course
Associated symptoms (dysphagia, otalgia, voice)
Personal habits (tobacco, alcohol)
Previous irradiation or surgery

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6
Q

Empirical antibiotics

A

Inflammatory mass suspected
Two week trial of antibiotics
Follow-up for further investigation

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7
Q

Special investigation

A
Fine needle aspiration cytology (FNAC)
Needle Core Biopsy 
-gives best result
Computed tomography (CT)
Magnetic resonance imaging (MRI)
Ultrasonography 
Radionucleotide scanning
PET scan
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8
Q

Fine needle aspiration FNA

A
Standard of diagnosis
Indications
-any neck mass that is not an obvious abscess
-persistence after a 2 week course of antibiotics
Small gauge needle 
-reduces bleeding
-seeding of tumor – not a concern 
No contraindications (vascular ?)
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9
Q

Fine needle aspiration biopsy

A
Proper collection required 
One-stop neck lump clinic
Under USS guidance 
Skilled cytopathologist/ Radiologist essential
On-site review best
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10
Q

Ultrasonography

A

Solid versus cystic masses
Congenital cysts from solid nodes/tumors
Noninvasive (paediatric)

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11
Q

Computed tomography

A

Distinguish cystic from solid
Extent of lesion
Vascularity (with contrast)
PET-CT Detection of unknown primary (metastatic)
Pathologic node (lucent, >1.5cm, loss of shape)
Avoid contrast in thyroid lesions

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12
Q

Magnetic resonance imagine

A

Similar information as CT
Better for upper neck and skull base
Vascular delineation with infusion

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13
Q

Magnetic resonance imagine

A

Similar information as CT
Better for upper neck and skull base
Vascular delineation with infusion

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14
Q

Radionucleotide scanning

A

thyroid and parathyroid masses
Location – glandular versus extra-glandular
Functional information
FNAC now preferred for thyroid nodules
-solitary nodules
-multinodular goiter with new increasing nodule
-Hashimoto’s with new nodule

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15
Q

Nodal mass workup in the adult

A

Any solid asymmetric mass MUST be considered a metastatic neoplastic lesion until proven otherwise
Asymptomatic cervical mass – 12% of cancer
~ 90% of these are SCC
Ipsilateral otalgia with normal otoscopy – direct attention to tonsil, tongue base, supraglottis and hypopharynx
Unilateral serous otitis – direct examination of nasopharynx
Panendoscopy, directed biopsy, synchronous primaries (10 to 20%), open excisional biopsy

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16
Q

Panendoscopy

A

FNA positive with no primary on repeat exam

FNA equivocal/negative in high risk patient

17
Q

Directed biopsy

A

All suspicious mucosal lesions
Areas of concern on CT/MRI
None observed – nasopharynx, tonsil (ipsilateral tonsillectomy for jugulodigastric nodes), base of tongue and piriforms

18
Q

Open excisional biopsy

A

Only if complete workup negative
Occurs in ~5% of patients
Be prepared for a complete neck dissection
Frozen section results (complete node excision)
-inflammatory or granulomatous – culture
-lymphoma or adenocarcinoma – close wound

19
Q

Primary tumours

A
Thyroid mass
Lymphoma
Salivary tumors
Lipoma
Carotid body and glomus tumors
Neurogenic tumors
20
Q

Thyroid masses

A
Leading cause of anterior neck masses
Children
-most common neoplastic condition
-male predominance
-higher incidence of malignancy
Adults
-female predominance
-mostly benign
21
Q

Thyroid masses - lymph node metastasis

A

Initial symptom in 15% of papillary carcinomas
40% with malignant nodules
Histologically (microscopic) in >90%

22
Q

Thyroid masses - FNAB has replaced USG and radionucleotide scanning

A

Decreases # of patients with surgery
Increased # of malignant tumors found at surgery
Doubled the # of cases followed up
Unsatisfactory aspirate – repeat in 1 month

23
Q

Lymphoma

A

More common in children and young adults
Up to 80% of children with Hodgkin’s have a neck mass
Signs and symptoms
-lateral neck mass only (discrete, rubbery, nontender)
-fever
-hepatosplenomegaly
-diffuse adenopathy
open biopsy
Full workup – CT scans of chest, abdomen, head and neck; bone marrow biopsy

24
Q

Salivary gland tumours

A

Enlarging mass anterior/inferior to ear or at the mandible angle is suspect
Benign
-asymptomatic except for mass
Malignant
-rapid growth, skin fixation, cranial nerve palsies
-FNAC: Accuracy >90% (sensitivity: ~90%; specificity: ~80%)
-CT/MRI – deep lobe tumors, intra vs. extra-parotid
Be prepared for total parotidectomy with possible facial nerve sacrifice

25
Carotid body tumour
Rare in children Pulsatile, compressible mass Mobile medial/lateral not superior/inferior Clinical diagnosis, confirmed by angiogram or CT Treatment -irradiation or close observation in the elderly -surgical resection for small tumors in young patients -->hypotensive anesthesia -->preoperative measurement of catecholamines
26
Lipoma
Soft, ill-defined mass Usually >35 years of age Asymptomatic Clinical diagnosis – confirmed by excision
27
Neurogenic tumours
Arise from neural crest derivatives Include schwannoma, neurofibroma, and malignant peripheral nerve sheath tumor Increased incidence in NF syndromes Schwannoma most common in head & neck
28
Schwannoma
``` Sporadic cases mostly 25 to 45% in neck when extracranial Most commonly between 20 and 50 years Usually mid-neck in poststyloid compartment Signs and symptoms -medial tonsillar displacement -hoarseness (vagus nerve) -Horner’s syndrome (sympathetic chain) ```
29
Congenital and developmental mass
Epidermal and sebaceous cysts Branchial cleft cysts Thyroglossal duct cyst Vascular tumors
30
Epidermal and sebaceous cysts
Most common congenital/developmental mass Older age groups Clinical diagnosis -elevation and movement of overlying skin -skin dimple or pore Excisional biopsy confirms
31
Branchial cleft cysts - cause - presentation - epidemiology - treatment
Branchial cleft anomalies 2nd cleft most common (95%) – tract medial to cnXII between internal and external carotids 1st cleft less common – close association with facial nerve possible 3rd and 4th clefts rarely reported Present in older children or young adults often following URI Most common as smooth, fluctuant mass underlying the SCM Skin erythema and tenderness if infected Treatment initial control of infection -surgical excision, including tract May necessitate a total parotidectomy (1st cleft)
32
Thyroglossal duct cyst
Most common congenital neck mass (70%) 50% present before age 20 Midline (75%) or near midline (25%) Usually just inferior to hyoid bone (65%) Elevates on swallowing/protrusion of tongue Treatment is surgical removal (Sis trunk) after resolution of any infection
33
Vascular tumours
Lymphangiomas and hemangiomas Usually within 1st year of life Hemangiomas often resolve spontaneously, while lymphangiomas remain unchanged CT/MRI may help define extent of disease Treatment -lymphangioma – surgical excision for easily accessible or lesions affecting vital functions; recurrence is common -hemangiomas – surgical excision reserved for those with rapid growth involving vital structures or associated thrombocytopenia that fails medical therapy (steroids, interferon)
34
Inflammatory disorders
Lymphadenitis | Granulomatous lymphadenitis
35
Lymphadenitis
Very common, especially within 1st decade Tender node with signs of systemic infection Directed antibiotic therapy with follow-up FNAB indications (pediatric) -actively infectious condition with no response -progressively enlarging -solitary and asymmetric nodal mass -supraclavicular mass (60% malignancy) -persistent nodal mass without active infection
36
Lymphadenopathy
Equivocal or suspicious FNAB in the pediatric nodal mass requires open excisional biopsy to rule out malignant or granulomatous disease
37
Granulomatous lymphadenitis
Infection develops over weeks to months Minimal systemic complaints or findings Common etiologies -TB, atypical TB, cat-scratch fever, actinomycosis, sarcoidosis Firm, relatively fixed node with injection of skin
38
Granulomatous lymphadenitis bacteria
``` Typical M. tuberculosis -more common in adults -posterior triangle nodes -rarely seen in our population -usually responds to anti-TB medications -may require excisional biopsy for further workup Atypical M. tuberculosis -pediatric age groups -anterior triangle nodes -brawny skin, induration and pain -usually responds to complete surgical excision or curettage Cat-scratch fever (Bartonella) -pediatric group -preauricular and submandibular nodes -spontaneous resolution with or without antibiotics ```