dermatoscope and its application in dermatology
TRANSCRIPT
Non invasive diagnostic
tool which visualizes subtle
clinical patterns of skin
lesions and subsurface skin
structures not normally
visible to the naked eye
HISTORY
1636- Christophorus Kolhaus
1893- Unna
1920- Johann Saphier “Dermatoscopy”
1950- Goldman “Dermoscopy”
PRINCIPLE
Trans illumination and magnification
Visibility of subsurface structures improved by LINKAGE fluids
Immersion oil
Olive oil
Mineral oil
Water
Antiseptic solution
Glycerin
Liquid paraffin
BASIC DESIGN
Achromatic lens -10
Inbuilt illuminating system-
Halogen lamps
Power supply
Inbuilt photography system
TYPES
Instruments without image capturing facility
Image capturing facility
Analytical capability
Videodermatoscope:
Polarised or non polarised video probe that
transmits images to monitor
STEREOMICROSCOPE
Allows an accurate binocular observation with different magnifications (X6-80). The illumination system includes a halogen lamp (12 V/50W)
TECHNIQUE
Non contact/Contact technique
Noncontact avoid risk of nosocomial
infection
Poor resolution & illumination
Contact plates- Graduated/ non
graduated
WHAT IS DERMOSCOPY IS USED FOR?
EVALUATING PIGMENTED SKIN LESIONSEVALUATING NONPIGMENTED SKIN LESIONSENTODERMOSCOPYTRICHOSCOPYONYCHOSCOPY
COLOUR
• Epidermis appears white
• Melanin
• Upper epidermis- Black
• DEJ- Light to dark brown
• Papillary dermis- Slate blue
• Reticular dermis- Steel blue
• White shades- Regression
melanoma, halo nevus, lichenoid keratosis, scars
• Red shades- Increased vascularisation, bleeding
PRIMARY CRITERIA
• Pigmented network lines and hypo pigmented holes
• Histologically- the length of rete ridges and to
distribution of melanin within keratinocytes of
epidermal rete ridges
• Hypo pigmented holes- supra papillary plates
PIGMENT NETWORK
MELANOCYTIC NAEVUS
• PN slightly pigmented
• Light brown network
• Thin lines and fade gradually at periphery
• Holes are regular and narrow
MELANOMA
• Thickened and
darkened
• Tree like branching at
periphery
• Ends abruptly
• Irregular holes
PSEUDOPIGMENT NETWORK
• Homogenous pigmentation interrupted by
hypopigmented hair follicles and sweat gland openings
• Uniform & symmetric in colour and pattern – Benign
• Nonuniform & asymmetric – Lentigo maligna
RADIAL STREAMING AND PSEUDOPODS
• Histologically- confluent junctional nests of atypical
melanocytes
• Linear extension of pigment at the periphery of
lesion
• Curved finger like projections, dark brown or black
PIGMENTED GLOBULES
• Round or oval, dark brown or black >1 mm
• Histologically -nests of pigmented melanocytes at
the junction in papillary dermis
• Milky red globules- nests of melanoma cells with
increased vascularity
SECONDARY CRITERIA
PIGMENTED DOTS
• Small round or irregularly shaped structures• Black or dark brown• Focal accumulations of free melanin or no. of highly
pigmented melanocytes in cornified layers of epidermis
BLUE- WHITE VEIL
• Ground glass area of pigmentation
• Blue grey to white in colour
• Compact orthokeratosis and hypergranulosis
• Confluent nests of heavily pigmented melanocytes in dermis
• Melanoma and Spitz nevi
BLUE GREY AREAS
• Colouration varying from grey-blue to deep grey
• Melanin/ hemosiderin within melanocytes and melanophages
• Melanoma regression
NEGATIVE PIGMENT NETWORK
• Lighter serpiginous lines making up cords and darker areas resembling elongated tubular or curved globular like structures
• Thin elongated hypo pigmented rete ridges accompanied by the presence of large nests of heavily pigmented melanocytic cells at dermal papillae
• Highly specific for melanoma
CHRYSALIS STRUCTURES
• Thick, short, bright, whitish linear structures
• Orthogonally oriented• Changes in composition
and orientation of collagen• Melanoma, Spitz nevi,
Dermatofibroma ,BCC
RED- BLACK LAGOONS
• Small, well defined, round or oval areas
• Thrombi within the vascular spaces of papillary dermis
• Hemangioma and angiokeratoma
VASCULAR PATTERNS
Kreusch& Koch Thick arborizing vessels- Pigmented BCC Corona vessels- Sebaceous hyperplasia Comma shaped- Dermal nevi
Point vessels- Melanocytic trs, Superficial epithelial trs Hairpin vessels- angiogenesis Linear irregular vessels- Malignant melanoma
PIGMENTED SKIN LESIONS
• MELANOCYTIC LESIONS• Melanoma• Benign naevi• Atypical naevus
• PIGMENTED BCC• SEBORRHOEIC KERATOSIS• VASCULAR LESIONS• MISCELLANEOUS
• Dermatofibroma • scc insitu
PATTERN ANALYSIS
Step 1: Melanocytic or Non melanocytic
Step 2: Identify the melanocytic lesion by CASH
MELANOCYTIC NAEVI
• Few colours, regular design, symmetrical pattern
MALIGNANT MELANOMA• Several colours, architectural disorder, asymmetry
heterogeneity
MOLE MAPPING
• To monitor atypical melanocytic lesions over time
• 3-6 monthly intervals in multiple atypical lesions
PIGMENTED BCC
Negative feature: Absence of pigment network + At least one Linear and arborizing telangiectasisLeaf-like or structure less areas on the periphery Multiple blue gray nodule Large blue gray ovoid nestsFocal ulcerationSpoke wheel areas
SEBORRHEIC KERATOSIS
• Multiple milia like cysts• Comedo-like openings• Hyperkeratosis/ fissures/
ridges• Light brown finger like
structures• Hairpin blood vessels• Cerebriform apperance
ACTINIC KERATOSIS
• Pink/ red pseudo network& erythema surrounding the hair follicle
• White to yellow surface scales• Linear or wavy vessels surrounding the hair follicle• Hair follicle openings filled with yellowish keratotic
plugs
SEBACEOUS HYPERPLASIA
• Central follicular opening &surrounding yellow nodule
• Vessels may extend to the centre of lesion
• Never arborizing
DERMATOFIBROMA
• Central white scar like patch
• Peripheral delicate network
• Absence of melanocytic features
PYOGENIC GRANULOMA
• Reddish homogenous areas
• White collarette• Ulceration• White rail lines
intersecting the lesion
KAPOSI’S SARCOMA
• Bluish-reddish colouration
• Rainbow pattern- most distinctive feature
• Scaly surface and small brown globules
LEISHMANIASIS
Orange- yellowish globules or areas, linear vessels, erythema, follicular plugging, hyperkeratosis, central ulceration
COMMON WART
• Multiple densely packed papillae with a central dot or loop, surrounded by whitish halo
• Small red to black dots
PLANTAR WART
• Prominent haemorrhage within yellowish papilliform surface
PLANE WART
Regularly distributed red dots, light brown to yellow background
GENITAL WART
Mosaic pattern, finger like or knob like pattern, nonspecific pattern
MOLLUSCUM CONTAGIOSUM
• Central pore or umbilication
• White to yellow amorphous structures
• Peripheral linear or branching vessels (red corona)
RARE SKIN INFECTIONS
TUNGIASIS Nodule with a central targetoid brownish ring, which in turn surrounds a central, black, pore.
CUTANEOUS LARVA MIGRANS Translucent brownish structure less areas in a segmental arrangement, corresponding to the body of the larva
MYCOSES
TINEA NIGRAReticulated pattern , consisting of superficial fine, wispy, light-brown strands or 'pigmented spicules’
ONYCHOMYCISIS White to yellow streaks and homogeneous areas in the distal nail plate.
NORMAL SCALP
• Red loops
• Perifollicular pigment network
• Follicular unit- 2-4 terminal hair
1-2 vellus hair
• Examine the nail plate from above as well as end-on
• Pigment in the top of the nail plate - proximal matrix
• Pigment at the bottom of the nail plate - distal matrix or
nail bed.
Melanocytic naevus of the nail apparatus is characterised by:
Regular parallel lines Brown background Granular inclusions
EPITHELIAL MELANIN
• Homogeneous longitudinal thin grey lines
• Light brown to dark grey background colour.
NAIL MATRIX MELANOMA
• Longitudinal brown to black parallel lines with irregular
colouration, spacing, or thickness
• Disruption of parallelism
• Brown background
• Hutchinson sign: pigmentation of cuticle
• Nail plate fissuring or destruction
Blood spots are well-circumscribed dots, globules or blotchesRed, purple, blue, brown or black
SUBUNGUAL HAEMORRHAGE
Benefits
• Dermoscopy increases the sensitivity for the
diagnosis of melanoma without decreasing the
specificity
• Dermoscopy reduces the number of unnecessary
biopsies.
• Dermoscopy allows digital surveillance and
monitoring of in patients with multiple atypical
nevi.
• Dermoscopy is useful in the diagnosis and
differentiation of nonmelanocytic benign and
malignant tumors
Limitations
• The diagnostic accuracy of dermoscopy- experience in the interpretation of dermoscopy .
• May fail to recognize melanomas that lack specific dermoscopic criteria (featureless melanomas) .
• Dermoscopy alone cannot establish the diagnosis of malignancy; histopathologic examination remains the gold standard.