
Dermoscopy, also known as dermatoscopy or epiluminescence microscopy, is a non-invasive diagnostic technique that enables clinicians to visualize subsurface skin structures not visible to the naked eye. By using specialized magnification and lighting systems, this method allows for detailed examination of pigmented and non-pigmented skin lesions, significantly improving the accuracy of melanoma and other skin cancer diagnoses. The importance of dermoscopy extends beyond mere magnification—it serves as a bridge between clinical examination and histopathological diagnosis, providing a window into the microscopic world of skin lesions without requiring invasive procedures. Studies from Hong Kong dermatology clinics demonstrate that dermoscopy increases diagnostic accuracy for malignant melanoma by 20-30% compared to naked-eye examination alone, making it an indispensable tool in modern dermatological practice.
The evolution of dermatoscope technology has produced various devices catering to different clinical needs and budgets. The main types include:
The diverse dermatoscope uses extend from primary care settings to specialized dermatology practices, with modern devices offering features like LED illumination, adjustable magnification (typically 10x-20x), portable designs, and smartphone compatibility. Essential equipment for effective dermoscopy practice includes not just the dermatoscope itself, but also immersion fluid for non-polarized devices, proper cleaning supplies to prevent cross-contamination, adequate storage solutions, and for digital systems, appropriate software for image management and analysis. The choice between devices depends on multiple factors including clinical setting, budget, and specific diagnostic requirements, with many Hong Kong dermatologists recommending hybrid systems for their versatility in examining both superficial and deeper structures.
Proper skin preparation forms the foundation of high-quality dermoscopic examination. The area of interest should be clean and free from cosmetics, ointments, or other substances that might interfere with visualization. For non-polarized dermoscopy, applying a suitable interface medium such as ultrasound gel, mineral oil, or 70% isopropyl alcohol is crucial to eliminate air gaps and surface reflection. The amount of fluid should be sufficient to create a uniform layer without excessive pooling, which can distort the image. In Hong Kong's humid climate, ensuring the skin is completely dry before application (except for the fluid itself) prevents additional moisture from diluting the interface medium and compromising image quality.
The technique of application varies between contact and non-contact approaches. Contact dermoscopy involves gently placing the dermatoscope directly on the skin surface with consistent, minimal pressure to avoid blanching vascular structures or distorting the lesion morphology. This method provides superior resolution for examining deeper structures and is particularly valuable for analyzing pigment networks and follicular openings. Non-contact dermoscopy, typically performed with polarized devices held slightly above the skin surface, preserves the integrity of fragile lesions and allows examination of ulcerated or inflamed lesions without risk of contamination or patient discomfort. Many experienced practitioners employ both techniques sequentially, as they reveal complementary information—contact mode excels at showing deeper structures while non-contact mode better visualizes superficial features and colors.
Optimizing lighting conditions represents another critical aspect of dermoscopic technique. Adequate, consistent illumination is essential, with many modern dermatoscides incorporating LED systems that provide bright, uniform lighting with accurate color representation. The angle of illumination can be adjusted to enhance specific features—oblique lighting may better reveal certain structural elements while direct lighting optimizes color assessment. Magnification settings typically range from 10x to 20x, with higher magnification useful for detailed analysis of specific structures but resulting in a smaller field of view. Beginners should start with intermediate magnification (approximately 10x) to maintain orientation within the lesion while still appreciating diagnostic details. The combination of proper lighting, appropriate magnification, and steady positioning creates optimal conditions for accurate lesion evaluation.
Developing proficiency in dermoscopic interpretation requires familiarity with numerous diagnostic structures and patterns. The pigment network—a grid-like pattern representing the rete ridges of the epidermis—is one of the most fundamental structures to recognize. A typical network appears as a honeycomb-like pattern of brown lines with hypopigmented holes, while atypical networks demonstrate irregularity in thickness, distribution, or coloration. Other crucial pigment-related structures include dots (small, round structures), globules (larger, oval or round structures), and streaks (linear extensions at the lesion periphery). Vascular patterns provide equally important diagnostic information, with morphology and distribution offering clues to the lesion's nature. Common vascular structures include comma vessels (typically seen in benign nevi), dotted vessels (often present in Spitz nevi and melanoma), and arborizing vessels (characteristic of basal cell carcinoma).
A systematic approach to image analysis prevents oversight of critical features and ensures consistent evaluation. The three-point checklist represents one of the simplest algorithms, assessing for asymmetry of structures, atypical network, and blue-white structures. More comprehensive systems like the ABCD rule of dermoscopy (analyzing Asymmetry, Border, Colors, and Differential structures) and the 7-point checklist provide structured methodologies for lesion evaluation. The CASH algorithm (Color, Architecture, Symmetry, and Homogeneity) offers another systematic framework. When examining dermoscopy images of melanoma, practitioners should specifically look for multiple colors (especially blue, gray, red, and white), structural asymmetry, irregular dots/globules, radial streaming, pseudopods, blue-white veil, regression structures, and atypical vascular patterns. Developing a consistent, step-by-step analytical routine ensures that no diagnostic element is overlooked, significantly improving diagnostic accuracy over time.
Beyond pigment and vascular patterns, numerous other structures contribute to the dermoscopic diagnosis. Leaf-like areas, spoke-wheel areas, and large blue-gray ovoid nests suggest basal cell carcinoma. Milia-like cysts and comedo-like openings typically indicate seborrheic keratosis. The specific features seen in dermoscopy of squamous cell carcinoma include keratin masses, scale, blood spots within keratin, white structureless areas, and glomerular or hairpin vessels. Recognition of these patterns requires extensive training and exposure to numerous cases, highlighting the importance of continued education in dermoscopic interpretation. Hong Kong dermatology training programs increasingly incorporate structured dermoscopy education, with studies showing diagnostic accuracy improvements of up to 40% following systematic training.
When evaluating moles and nevi, dermoscopy reveals patterns that correlate with histological architecture. Common acquired nevi typically display one of five global patterns: reticular (network pattern throughout), globular (nested globules), starburst (radial symmetry at periphery), homogeneous (structureless pigmentation), or parallel pattern (specific to acral sites). Benign nevi generally demonstrate symmetry, uniform network pattern, regular dots and globules, and minimal color variation. Concerning features that warrant closer examination include focal network thickening or thinning, irregularly distributed dots/globules, peripheral structural changes, and color variegation. The management of melanocytic lesions depends largely on whether they follow a benign pattern or display features suggestive of dysplasia or malignancy.
Seborrheic keratoses present with characteristic dermoscopic features that often allow for confident diagnosis without biopsy. These include:
Other benign lesions demonstrate equally distinctive patterns. Dermatofibromas typically show a central white scar-like patch with a peripheral delicate pigment network. Hemangiomas appear as well-demarcated, red to purple lacunae separated by white septa. Solar lentigines demonstrate a moth-eaten border and faint pseudonetwork on facial skin. Recognizing these benign patterns prevents unnecessary procedures while ensuring malignant lesions receive appropriate attention.
Suspicious features that should prompt consideration of referral or biopsy include the "ugly duckling" sign (a lesion that looks different from the patient's other nevi), rapid change in size or appearance, and specific dermoscopic structures associated with malignancy. For melanoma, these include atypical pigment network, irregular streaks, blue-white veil, negative network, shiny white structures, and atypical vascular patterns. In the context of dermoscopy of squamous cell carcinoma, concerning features include clustered vascular patterns (especially hairpin or glomerular vessels), scale, blood spots within keratin, and white structureless areas. Basal cell carcinoma features include leaf-like structures, large blue-gray ovoid nests, arborizing vessels, and ulceration. Hong Kong cancer registry data indicates that incorporating dermoscopic analysis into skin cancer screening has improved early detection rates for melanoma by approximately 25% over the past decade.
Mastering the differential use of polarized and non-polarized light significantly enhances diagnostic capability. Non-polarized dermoscopy (requiring contact and fluid) provides superior visualization of deeper structures such as the pigment network, horn cysts, and comedo-like openings by eliminating surface reflection. Polarized dermoscopy (either contact or non-contact) better reveals superficial features including colors, scale, vascular patterns, and white structures such as regression areas and shiny white lines. The combination of both modalities offers complementary information—for example, non-polarized light might reveal a subtle pigment network while polarized light better demonstrates the vascular pattern in the same lesion. Many hybrid devices allow instant switching between modes, enabling direct comparison and more comprehensive assessment.
Dermoscopic algorithms provide structured approaches to lesion analysis, each with specific strengths and applications. The ABCD rule assigns numerical values to Asymmetry (0-2 points), Border abruptness (0-8 points), Color variety (1-6 points), and Differential structures (1-5 points), with total scores indicating probability of malignancy. The 7-point checklist focuses on seven specific criteria (atypical pigment network, blue-whitish veil, atypical vascular pattern, irregular streaks, irregular dots/globules, irregular blotches, and regression structures), with a score of 3 or more suggesting melanoma. The Menzies method evaluates for negative features (symmetry of pattern and presence of only a single color) and positive features (blue-white veil, multiple brown dots, pseudopods, radial streaming, scar-like depigmentation, peripheral black dots/globules, multiple colors, multiple blue/gray dots, and broad network). Understanding these various approaches allows practitioners to select the most appropriate algorithm for specific clinical situations.
Numerous resources support ongoing dermoscopy education and skill development. Recommended textbooks include "Dermoscopy: The Pattern Approach" by Pehamberger et al., "Atlas of Dermoscopy" by Marghoob et al., and "Dermoscopy of Pigmented Skin Lesions" by Argenziano et al. Online platforms such as DermNet New Zealand, the International Dermoscopy Society website, and various smartphone applications provide extensive image libraries and educational content. Structured courses offered through dermatology societies and academic institutions, including those available through the Hong Kong College of Dermatologists, provide hands-on training and certification opportunities. Regular participation in dermoscopy case discussions, whether in person or through online forums, reinforces pattern recognition and diagnostic reasoning. The integration of artificial intelligence in dermoscopy represents an emerging resource, with several systems now demonstrating diagnostic accuracy comparable to experienced dermatologists for certain lesion types, though human oversight remains essential.