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    Diagnostic Dermoscopy: The Illustrated Guide
    Diagnostic Dermoscopy: The Illustrated Guide
    Diagnostic Dermoscopy: The Illustrated Guide
    Ebook513 pages1 hour

    Diagnostic Dermoscopy: The Illustrated Guide

    By Jonathan Bowling

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    About this ebook

    Ideal for clinic use, both for diagnosis and for explaining to the patient, this guide provides:

    • A quick reference atlas guide to the diagnosis skin lesions, especially, but not limited to, those that are cancerous
    • Icons for each condition linked to high definition dermoscopy and clinical photographs
    • Real dermatoscopic images and the associated clinical photographs on the page opposite
    LanguageEnglish
    PublisherWiley
    Release dateOct 18, 2011
    ISBN9781444329858
    Diagnostic Dermoscopy: The Illustrated Guide

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      Book preview

      Diagnostic Dermoscopy - Jonathan Bowling

      Preface

      Skin is a dynamic canvas upon which life paints its picture. Each individual has a unique ‘picture’ reflecting his or her age, skin phototype and UV exposure, as well as genetic and acquired influences. However, unlike a canvas hanging on the wall, this ‘picture’ is not static; it is biologically active and therefore changes and evolves through life.

      Benign naevi dominate childhood and adulthood; however, this dominance is gradually replaced by seborrhoeic keratoses, which become more numerous later in life. Additionally, the accompanying increase in vascular lesions and potential for skin malignancy through life makes for a complex ‘picture’, rich in colours, shapes and textures.

      To interpret the ‘picture’ accurately, one must understand not only the macro, the shape, size, colour and age of the canvas, but the micro, the brushstrokes used to create the detail in these patterns and colours. This micro detail is often obscured by light reflecting off the skin surface, which may explain why many different lesions look similar. By using dermoscopy, we can overcome this optical challenge, revealing the diagnostic detail within lesions – this is diagnostic dermoscopy.

      Two important concepts are helpful in increasing diagnostic accuracy:

      1. Tumours grow – they do not appear. We should therefore look for the diagnostic detail present in all lesions to find the small tumours.

      2. Tumours evolve – they are not static. We should therefore accept that the detail seen may be influenced by many external and internal factors.

      Increasing our understanding of the variety of ways in which tumours present will increase our diagnostic accuracy. This book therefore aims to illustrate the many ways in which different tumours present, complete with the diagnostic dermoscopic features to aid diagnosis.

      Whenever possible, examples are shown for lesions that vary for size, shape, anatomical site, skin phototype and, when feasible, evolution with time. Hopefully, the diagnostic detail illustrated in this book will lead to improved skin lesion diagnosis and earlier diagnosis of skin cancer.

      Since the introduction of dermoscopy into clinical practice in the 1990s, our understanding of this diagnostic technique has increased exponentially. Credit should be given to the dermoscopy pioneers, who reshaped the diagnostic world through research, education and innovation. Their endeavours have proven that dermoscopy is without doubt the gold standard in clinical diagnosis, a diagnostic technique practised in over 100 countries worldwide.

      However, it is very important to remember that dermoscopy should not be practised in isolation. A clinical diagnosis is the summation of information gained from:

      1. Clinical history

      2. Clinical examination

      3. Dermoscopic examination.

      Diagnosis is in the detail; therefore, it is essential to combine all clinical skills and not use any in isolation. This book only provides information on one component of skin lesion diagnosis. We also know that tumours, especially melanoma, may take time to develop dermoscopic features, and may even mimic benign lesions. Additionally, in established tumours many dermoscopic features may be absent. Therefore, this book is aimed as a guide to be used in the clinical arena, to augment clinical decision-making and not to replace clinical judgement.

      Jonathan Bowling

      Further information and examples of conditions described in this book can be found at: www.dermoscopy.co.uk

      1 Introduction to Dermoscopy

      Introduction to Dermoscopy

      Introduction

      Viewing the invisible world …

      Instruments

      Non-polarised devices (oil immersion/contact)

      Polarised devices

      Hybrid devices

      Which device is best?

      Device comparisons I

      The Heine Delta 20 versus the DermLite II PRO HR

      Chrysalis structures

      Device comparisons II

      Comparisons of contact versus non-contact polarisation: structures in a seborrhoeic keratosis

      Comparison of the polarising mode and the non-polarising mode – the DermLite II Hybrid m

      Device comparisons III

      DermLite DL3 versus DermLite II PRO HR versus Heine Delta 20

      Device maintenance tips

      Normal skin

      Skin phototype I

      Skin phototype V

      Photodamaged skin I

      Acute photodamage

      Chronic photodamage

      Photodamaged skin II

      Examples of photodamaged skin

      Pigment depth and colour

      The dermoscopic alphabet

      Introduction to Dermoscopy

      Introduction

      The ‘art’ of dermatological diagnosis is a complex process that requires many skills.

      If dermatologists were to be described in a single word, they would be ‘diagnosticians’; the ‘art’ of dermatological diagnosis requires all the skills of a physician in addition to the eyes of a hawk, for lesion diagnosis cannot be made by history alone.

      Most lesions that from afar look indistinct become obviously benign or malign on closer inspection. However, there are plenty of lesions where close visual inspection is still not enough. How do we approach these lesions? Tools to aid diagnosis, such as the magnifying lens and bright light sources, can help or – failing that – a biopsy, whereby the diagnosis appears as a line on the histology report. However, simple adjustments to our clinical practice may be all that is required to improve our diagnostic ability.

      To begin with, we should search for clues to diagnosis, the diagnostic detail in lesions, and not just rely upon rather crude data such as shape, size and colour for a diagnosis. Although these crude parameters are often all that is required for a diagnosis, relying solely upon them will limit your diagnostic accuracy. Imagine an art dealer investing in a painting based solely upon the shape, size, age and colour of the picture frame, without appreciating the detail in the brushstrokes of the canvas. These dermatological ‘brushstrokes’ are the morphological structures that comprise skin tumours, and unfortunately many of them are invisible to the naked eye.

      Viewing the invisible world …

      Two barriers need to be overcome.

      First, the rough surface of the stratum corneum causes light to scatter, reducing light penetration into the skin. This scattering of light impairs the view of the morphological structures hidden within a lesion. This can be illustrated by light reflecting off the surface of this rippled pool (a), distorting the detail seen of the tiles underneath. However, if the surface is calm (b), more light penetrates deeper into the pool before being reflected and greater detail can be seen:

      This surface scattering of light can be overcome in the clinical arena by contact with the skin using an interface medium or by means of polarised light.

      The second point to consider is magnification. The benefits of magnification to augment skin diagnosis have long been recognised. Although we believe our eyes to show all the detail required for diagnosis, the truth is that they are limited. To illustrate the point, the microprint in this banknote is invisible to the naked eye (c), but is clearly visible with magnification (d):

      The combination of increasing light penetration into a lesion and magnification is dermoscopy.

      Dermoscopy is now used in over a hundred countries worldwide, with unequivocal evidence to support its use in skin lesion diagnosis.

      The structures seen with dermoscopy equate to a histopathological correlate, and therefore an understanding of this relationship will help in diagnosis.

      Throughout this book, examples are provided to illustrate the spectrum of clinical presentation and the variability of morphological structures seen for any diagnosis.

      Instruments

      Problem: Why do most moles just look brown? The stratum corneum reflects light, reducing the ability to see detail of structures in the underlying skin. Thus most moles look brown, with relatively little detail. The detail exists; it is just not visible.

      Theory: If we are able to overcome the refractive properties of the stratum corneum, greater detail in the underlying skin can be observed. This is the underlying concept upon which dermoscopy is based. This can be achieved by the simple application of an interface medium directly to the skin, such as alcohol gel. Any bright light source and magnification lens can then be used to see increased detail in the skin, including the morphological detail and pigment distribution within naevi. However, the use of gel

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