Head/neck/soft Tissue Flashcards

1
Q

Describe the lymph node levels in neck? What are radical, modified radical and selective neck dissection?

A

There are 7 levels

  1. submental (1a) and submandibular (1b)
  2. Upper third of IJV (hyoid to base of skull (2a = anterior to XI nv; 2b = posterior to XI nerve)
  3. middle third of IJV (Hyoid to Cricoid)
  4. Lower third of IJV (Hyoid to clavicle)
  5. posterior to SCM (5a= above cricoid; 5b = below cricoid)
  6. Central (between carotids and innominate)
  7. Superior mediastinum

Radical neck dissection = removal of all fibrofatty tissue on levels 1 -5 plus SCM, IJV and XI nerve

Modified radical = all fibrofatty tissue in levels 1-5 but any or all of SCM, IJV and XI preserved

Selective neck dissection = dissection of all fibrofatty structures in a selected compartment, preserving all critical structures

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2
Q

what are the layers of epidermis?

A

Come, let’s go sun bath

C - stratum corneum

L - lucidum

G - granulosum

S - spinosum

B - basale

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3
Q

ABCDE of melanoma

A

A - asymmetry B - border C - colour D - Diameter >6mm E - Evolution

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4
Q

What are the high risk features melanoma

A

LN metastasis

Breslow thickness

Mitosis

Ulceration

Age (more is worse)

Gender (men worse)

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5
Q

What are risk factors for melanoma?

A

M-FRISKx

Moles (multiple, >50) - dysplastic naevus

F Freckles

R - race (whites) and red hair

I - Immunosuppressed

S - Sun damage

K - Kindred (fam history)

Xeroderma pigmentosum

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6
Q

What are the types of melanoma

A

Melanoma LANDS on the skin

L - lentigo maligna (head and face, late vertical phase growth)

A - Acral (subungal, feet, hands)

N - Nodular (early vertical phase, may be amelanocytic)

D - Desmoplastic (with stromal fibrosis, neurotrophic)

S - Superficial spreading (commonest)

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7
Q

What is Breslow thickness?

A

This measures the depth of the tumor cell invasion from stratum granulosum to the deepest point of invasion. It correlates with the prognosis and helps guide treatment. <1mm (thin) 1.1 - 3.9 mm (Intermediate. In MSLT1 - 1.2 -3.5 mm was designated intermediate) >4 mm (thick)

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8
Q

Indications and technique for SNB in melanoma

A

Indications: I use the melanoma institute sentinel node metastasis risk prediction tool to calculate the probability of melanoma having spread to the node. SNB is typically indicated if the risk is >10%; but decision needs to be tailored to individual patients.

In general terms, the results of MSLT1 trail confirms that SNB for intermediate thickness melanoma provides melanoma specific survival advantage. Performing SNB in very thin or thick melanoma is controversial. There is evidence that patients with thin melanoma >0.75mm may only benefit form SNB if they have high risk features. For thick Melanoma, SNB may help prognosticate but does not alter the final outcome.

Technique: Lymphoscintigraphy is performed pre-op to identify which basin to operate. Patent blue or isosulfan blue is injected intradermally around the lesion/scar after anaesthesia. Intraoperatively, hot and or blue node is then removed being careful not to remove more than 2-3 nodes. Frozen sections are usually not sent because of difficulty in diagnosing melanoma on frozen section.

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9
Q

What were the outcomes of MSLT 1 and MSLT 2 trials?

A

MSLT1 - 2001 patients with intermediate (1.2 - 3.5mm) melanoma and thick melanoma (>3.5mm) were randomised them into SNB vs observation for nodes. Results at 10-year show disease free survival advantage in intermediate group but not thick group. For intermediate melanoma 16% had a positive SNB and underwent lymphadenectomy. The melanoma specific survival advantage was only seen in these patients, not for the whole group of SNB.

MSLTII - 1934 patients with melanoma >1.2mm or Clark level 3-5 or ulceration and +SNB randomized to elective node dissection vs no further surgery. Interim results at 4.3yrs show melanoma specific survival to be same, disease-free survival better in node dissection group but also significant comorbidities (lymphedema 24% vs 6 %) in the same group. It has not been possible to isolate a specific group of patients who would benefit from CLND. For the observation group, surveillance was performed with US scans 4 monthly for 2 years, 6 monthly for 3-5 yrs and then annually. most patients had <1mm mets in the lymph node.

Findings of the MSLT II trial is echoed by the De-COG-SLT trial in which 483 patients with melanoma were randomised to receive CLND vs observation. There was no difference in the overall survival or metastasis free survival.

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10
Q

What structures are at risk during submandibular gland surgery?

A

Superficial to the gland

  • Marginal mandibular nv
  • cervical branch of VII nv

Superficial lobe

  • Facial artery
  • Facial V

Deep lobe

  • Lingual nerve
  • XII nerve
  • Ranine vein
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11
Q

Describe the staging for cutaneous melanoma

A

All T stages subclassified a= no ulcer, b = ulceration

T1 - <1mm deep

T2 - 1-2 mm

T3 - 2-4

T4 >4

N1 - 1 (node or intransit met or satellite melanoma)

N2 - 2-3

N3 - 4 or more

Stage 1 (early local) = T1, t2a

Stage 2 (advanced local) = T2b - T4b, N0, MO

Stage 3 - Node positive (or intransit or satellite mets)

Stage 4 - metastatic

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12
Q

What are the adjuvant therapy options for melanoma

A

Depends on local protocols/ availability/ tumour characters.

Adjuvant therapy is indicated in stage 3 - 4 disease (nodes or mets)

Surgery

  • Oligometastatic disease that is resectable (best outcome)

Targeted therapy

  • **MAPK pathway - _(_BRAF+MEK - inhibitors if mutation present)
  • KIT - inhibitors (If mutated)

Immune therapy

Immune checkpoint therapy - blocks natural checkpoint for T-cell productions thereby unleashes massive number of T cells. Combination of CTLA4 + PD1 is recommended.

  • ​CTLA4 blockers - Ipilimumab (Yervoy)
  • PD-1 blocker - Pembrozulimab (keytruda), Nivolumab (Opdivo)

Isolated limb infusion using Melphalan

  • Papaverine used as vasodilator and heparin used as anticoagulant before melphalan infusion.

limited availability, no survival benefit but improves local control.

Radiotherapy

  • Palliative control of local disease

Chemotherapy

  • Limited role due to poor outcomes
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13
Q

What is hidradenitis suppurativa

A

It is a chronic inflammatory condition of the folliculo-pilo-sebaceous unit of the skin and is characterised by painful, nodular pustules with scarring and fistulation in the intertriginous areas of the body

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14
Q

What % of patients with Melanoma have positive SNB?

A

Intermediate thickness (1.2mm - 3.5mm)

  • approx 20% will have lymph node mets
  • SNB will identify approx 16-17 % patients
  • 3-4% will have a false negative SNB

Thick melanoma (>3.5mm)

  • approx 40 % will have a LN met

The risk can be predicted using the melanoma institute sentinel node metastasis risk prediction tool.

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15
Q

Factors affecting prognosis in metastatic melanoma

A
  1. LDH
  2. performance status
  3. < 3 sites with metastatic disease
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16
Q

Investigations for evaluation of metastatic melanoma

A

CT CAP

MRI Brain

LDH

Driver mutations

  • BRAF for all cutaneous melanomas
  • KIT for mucosal and acral melanomas
17
Q

satellite vs in transit mets for melanoma - what is the distinction. How does treatment differ from primary melanoma?

A

Both represent intralymphatic spread.

Satellite is within 2 cm of the primary melanoma and in transit is beyond 2 cm but not beyond the nodal basin

Treatment of these differs from the primary in several ways:

  1. margin - only a clear margin is needed
  2. multiple surgical excisions may be needed
  3. Effect of immunotherapy is not known and trials are on way
  4. treatment = surgery -> isolated limp perfusion or infusion (melphalan) vs systemic therapy (checkpoint inhibitors, targeted therapy and BRAF inhibitors)-> radiation
  5. systemic therapy results in sustained but less predictable response rate than ILP/ILI