Screening Children Part 2 - Spitzoid Nevi Flashcards
Dermatopathology spitz nevus
Proliferation of large spindle and epithelioid cells
Junctional, dermal, or compound
Associated with conspicuous epidermal hyperkeratosis or acanthosis
Little or no pigment deposition
Dermatopathology Reed Nevus
Pigmented spindle cell nevus Heavily pigmented Monomorphic Small to medium spindle melanocytes Bandlike dermal infiltration of melanophages
Do we distinguish between pigmented spitz and reed nevi
NO because they are same from clinical point of view
How do non pigmented spitz nevi present
Pigmented lesion
Reddish papules or nodules
Very visible brown to black pigmentation
Spitz nevi, preferential sites
Face
Acral sites
Buttocks
Spitz nevi, dermoscopic patterns
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.
Spitz nevus Ddx
Viral warts - splinter hemorrhages
Xanthogranulma - yellowish appearance clinically and dermoscopically
Pilomatrixoma - nodular, firm, bluish component
Pyogenic granuloma - impossible to distinguish from spitz nevus
Evolution spitz nevi
Starburst
Globular
Starburst
Management Spitz nevi
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
Spitz nevi excluded for conservative follow up
Nodular lesions
Atypical lesions
Multi-component pattern
Follow up is becoming standard of care in …..
Flat symmetrical spitzoid lesions in patients < 12 years
What is atypical spitz tumour
Histopathological features not sufficient for diagnosis of melanoma, capable of nodal metastases, with no further spread
Incidence AST
6-8% of Spitz nevi
Clinical presentation AST
First 2 decades life Medium to large <7 mm Nodular Rarely ulcerated Mostly hypopigmented or amelanotic cutaneous lesion
AST controversies
- AST are biologically benign nevi that have features in common with melanoma
- AST are biological intermediates between nevi and conventional melanoma
- AST represent a subset of melanomas with a better prognosis than conventional melanoma.