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AlexanderSalava
VivianLindholm

Dermatoscopy

Essentials

  • Dermatoscopy is used for assessing skin lesions.
  • It can improve the diagnostic accuracy of assessing pigmented lesions (early detection of melanoma).
  • Dermatoscopy will show typical structures in many benign skin lesions. Seborrhoeic keratosis and haemangioma, for instance, are usually easy to distinguish from pigmented lesions.
  • A dermatoscope is a dermatologist's routine tool. Learning to use a dermatoscope is also recommended for primary health care providers.
  • This article deals with the most typical indications for and basics of dermatoscopy that are important for general practitioners.

General remarks

  • Synonyms: dermoscopy, epiluminescence microscopy
  • The clinical picture, patient history and experience in using a dermatoscope are important. If the diagnosis is uncertain, a biopsy specimen should be taken (histological confirmation).
  • Dermatoscopy is based on microscopic examination (usually 10-fold magnification) of the skin surface.
  • Equipment: lighting system and loupe
  • Either a contact (with fluid between the dermatoscope and skin) or noncontact method can be used.
  • Dermatoscopy is always just an assistive tool. If there is a discrepancy between the clinical picture and the dermatoscopy finding, histological confirmation is recommended.
  • Dermatoscopy requires practice and experience of the correlation between the dermatoscopic picture and the histological finding (removal and histological assessment of the skin lesion).
  • The lesion should be removed in any case if malignancy is suspected based on the clinical picture, patient history and/or risk factors Naevi (Moles).

Structures seen on dermatoscopy

  • Symmetry or asymmetry (in the shape, colour or pigment structures of skin lesions)
  • Homogeneity/heterogeneity of the lesion
  • Distribution of pigment and pigment structures: brown streaks, dots, globules, unstructured areas
  • Superficial keratin structures: small white cysts, crypts, fissures
  • Appearance and distribution of blood vessels (even/uneven, atypical vessels)
  • Structures at the lesion margin (unclearly/clearly demarcated, radial streaks or digitate prominences)
  • Ulceration, blue-white veil-like structure

The biphasic algorithm of melanoma diagnosis

  • A biphasic algorithm can be used to diagnose melanoma. In the first phase, it should be clarified whether the lesion is melanocytic or of some other type (such as seborrhoeic keratosis, dermatofibroma, basal cell carcinoma, haemangioma).
    • 1st phase: typical features of melanocytic lesions
      • Pigment network (Image F1)
      • Aggregated brown or black globules (Image F2)
      • Special features: parallel pattern on palms and soles, asymmetrically pigmented follicular openings on facial skin, homogeneous steel-blue colour of blue naevus
    • 2nd phase: assessment of the malignancy of the pigmented lesion
    • The 3-stage checklist below has proved to be the most sensitive and simplest method.
      • Asymmetry (asymmetry of colour or structure in one or two axes)
      • Atypical network: pigment network with irregular holes and thick streaks
      • Blue-white structures: blue-white veil or white, cicatricial areas of regression
    • The aim of the checklist is to identify melanoma.
    • If 2 or more of the listed items are checked, melanoma is highly probable and the lesion should be removed.
  • Quick assessment of malignancy of a skin lesion: ”chaos and clues”
    • The “chaos and clues” method can be applied to any pigmented lesion. It can be used to diagnose not only melanoma but also pigmented basal and squamous cell carcinomas and pigmented Bowen's disease. The aim is not so much to obtain a precise diagnosis but to find out quickly whether a biopsy should be taken of the lesion.
    • Chaos refers to asymmetry of structures and colours. If there are different colours or structures on the two sides separated by a line drawn through a lesion , the lesion is asymmetric and chaotic.
    • If, regardless of the shape of the lesion, there is only one structure and one colour, the lesion is not chaotic.
    • However, exceptions to this rule include nodular lesions, small new lesions and lesions with a history of change, pigmented naevi on hands or feet with pigment on rete ridges, and any facial lesion where grey colour is detected by dermatoscopy.

Typical dermatoscopic features

Malignant skin lesions

  • Melanoma (Images F3 F4 F5 F6 F7 F8 F9 F10)
  • Asymmetry/polymorphism of the pigment network, colour and form
  • Blue-white veil
  • Areas of regression; no pigment network
  • Unstructured dark area; pigment network not discernible
  • Abundant black dots asymmetrically distributed over the lesion or at its margins
    • Black dots occur in growing pigmented lesions. If the dots are evenly distributed, particularly in a naevus in a young person, it is usually a benign lesion.
    • If the dots are asymmetrically situated, the lesion should be removed.
  • Asymmetrically distributed radial streaming or pseudopods at the margins of the lesion; Images F11 F5
  • In acral lentiginous melanoma, pigment on the sole or palm is linearly located in a parallel ridge pattern.
  • In facial lentigo maligna melanoma, pigment may occur in an annular-granular pattern around follicular openings or it may completely cover some follicular openings (Images F6 F7).
  • It is quite challenging to identify amelanotic melanoma because in most cases the pigment network is completely absent. Pink, unstructured, unclear lesions should always be removed (Image F8).
  • (Pigmented) basal cell carcinoma (Images F12 F13)
    • In pigmented basal cell carcinoma, brown or black leaf-like structures, spoke wheel areas or pigmented elliptical areas may be seen. Additional typical features of basal cell carcinoma include arborizing blood vessels.
    • Nodular basal cell carcinoma often shows shiny white blotches and strands with ulceration in the centre.
  • Dermatoscopy of squamous cell carcinoma and preceding precancerous lesions is challenging and not completely unequivocal. Here the clinical picture is more important for the beginner.

Benign skin lesions

  • In this section, we first present a skin lesion visible to the naked eye and then corresponding dermatoscopic pictures.
  • Pigmented naevi (Images F14 F2 F15)
    • Regular honeycomb-structured pigment network or in globular naevi regular globules (cobblestone structure)
    • Regularly distributed black dots on the lesion or at the margins
    • In acral naevi, pigment occurs in a parallel furrow pattern (Image F16).
    • In facial solar lentigo, light, sharply demarcated pigment occurs symmetrically around follicular openings.
  • Blue naevus (Images F17 F18)
    • Distinctly defined, blueish, unstructured skin lesion
    • Blue naevi should always be removed because melanoma may mimic them.
  • Seborrhoeic keratosis (Images F19 F20 F21 F22)
    • Sharply demarcated, cloudy translucent lesion with ridge-furrow structure, cerebriform surface (mimicking cerebral gyri) or cobblestone structure
    • In addition, there are often milia-like white cysts and/or comedo-like black openings.
    • In thin seborrhoeic keratosis, typical marginal structures, such as moth-eaten border or fingerprint-like structures can be seen.
  • Haemangiomas, cherry angioma (Images F23 F15 F24 F25)
    • Several dark red, blue or purple large lagoons (lacunae) of the same colour
    • Cherry angiomas are homogeneous, bright red lesions.
  • Dermatofibroma (Images F26 F1)
    • Regular, stellate white streaks from the centre of the lesion towards the periphery that may be surrounded by a delicate light brown pigment network
  • Sebaceous hyperplasia
    • Consists of white or yellowish globules. Delicate crowning vessels from the periphery towards the centre but not reaching it.
  • Subungual haematoma (Images F27 F28)
    • Dark red lagoons can be seen underneath the nail. In melanocytic lesions, pigmentation can be seen towards the base of the nail.

    References

    • International Dermoscopy Society (IDS) http://dermoscopedia.org
    • Usatine RP, Shama LK, Marghoob AA et al. Dermoscopy in family medicine: A primer. J Fam Pract 2018;67(12):E1-E11. [PubMed]
    • Kittler H, Marghoob AA, Argenziano G et al. Standardization of terminology in dermoscopy/dermatoscopy: Results of the third consensus conference of the International Society of Dermoscopy. J Am Acad Dermatol 2016;74(6):1093-106. [PubMed]
    • Chen X, Lu Q, Chen C et al. Recent developments in dermoscopy for dermatology. J Cosmet Dermatol 2021;20(6):1611-1617. [PubMed]
    • Pampena R, Lai M, Lombardi M et al. Clinical and Dermoscopic Features Associated With Difficult-to-Recognize Variants of Cutaneous Melanoma: A Systematic Review. JAMA Dermatol 2020;156(4):430-439. [PubMed]
    • Jones OT, Jurascheck LC, van Melle MA et al. Dermoscopy for melanoma detection and triage in primary care: a systematic review. BMJ Open 2019;9(8):e027529. [PubMed]
    • Dinnes J, Deeks JJ, Chuchu N et al. Dermoscopy, with and without visual inspection, for diagnosing melanoma in adults. Cochrane Database Syst Rev 2018;12:CD011902. [PubMed]

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