Screening Children Part 2 - Spitzoid Nevi Flashcards

1
Q

Dermatopathology spitz nevus

A

Proliferation of large spindle and epithelioid cells
Junctional, dermal, or compound
Associated with conspicuous epidermal hyperkeratosis or acanthosis
Little or no pigment deposition

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2
Q

Dermatopathology Reed Nevus

A
Pigmented spindle cell nevus
Heavily pigmented
Monomorphic
Small to medium spindle melanocytes
Bandlike dermal infiltration of melanophages
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3
Q

Do we distinguish between pigmented spitz and reed nevi

A

NO because they are same from clinical point of view

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4
Q

How do non pigmented spitz nevi present

Pigmented lesion

A

Reddish papules or nodules

Very visible brown to black pigmentation

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5
Q

Spitz nevi, preferential sites

A

Face
Acral sites
Buttocks

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6
Q

Spitz nevi, dermoscopic patterns

A

Reticular pigmentation with dotted vessels
Dotted vessels in pink background in non pigmented lesion
Pigmented lesion usually present with starburst pattern - peripheral symmetrical streaks around lesion
Or globular pattern with big brown to black globules
Or the so called superficial black network in heavily pigmented lesions area of hyperkeratosis with superficial black network visible on surface of lesion
Atypical or multi-component pattern which resembles a melanoma.

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7
Q

Spitz nevus Ddx

A

Viral warts - splinter hemorrhages
Xanthogranulma - yellowish appearance clinically and dermoscopically
Pilomatrixoma - nodular, firm, bluish component
Pyogenic granuloma - impossible to distinguish from spitz nevus

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8
Q

Evolution spitz nevi

A

Starburst
Globular
Starburst

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9
Q

Management Spitz nevi

A

Children < 12:Dermoscopy follow up every 6-12 months for 2-3 years and then once a year until stabilization or involution.
In children 12 and older follow every year for lesions with typical clinical and dermoscopic features and surgical removal of all Spitz nevi with atypical features

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10
Q

Spitz nevi excluded for conservative follow up

A

Nodular lesions
Atypical lesions
Multi-component pattern

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11
Q

Follow up is becoming standard of care in …..

A

Flat symmetrical spitzoid lesions in patients < 12 years

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12
Q

What is atypical spitz tumour

A

Histopathological features not sufficient for diagnosis of melanoma, capable of nodal metastases, with no further spread

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13
Q

Incidence AST

A

6-8% of Spitz nevi

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14
Q

Clinical presentation AST

A
First 2 decades life
Medium to large <7 mm
Nodular
Rarely ulcerated
Mostly hypopigmented or amelanotic cutaneous lesion
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15
Q

AST controversies

A
  1. AST are biologically benign nevi that have features in common with melanoma
  2. AST are biological intermediates between nevi and conventional melanoma
  3. AST represent a subset of melanomas with a better prognosis than conventional melanoma.
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16
Q

Clinical features that increase the risk of AST

A

Nodular
Non pigmented
Ulcerated

17
Q

Does typical non pigmented spitzoid pattern r/o AST

A

No

18
Q

Pink nodule with dotted vessels or atypical vessels with milky red colour has the following Ddx

A

Spitz nevus
AST
Melanoma

19
Q

Management AST

A

Review histopathological

Wide excision

20
Q

FISH probes are used to

A

Categorize risk of metastases

21
Q

AST and sentinel lymph node diagnostic

A

No prognostic value

Not performed

22
Q

What % AST have positive sentinel node bx

A

39%

23
Q

AST prognosis

A

99% survival at 5 years.