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Dermoscopy Update: Review of its Extradiagnostic and Expanding Indications and Future Prospects

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Abstract

The technique of dermoscopy has come a long way since its inception for characterization of suspicious nevi for early detection of dysplastic changes in predisposed individuals. Not only has its scope expanded to aid in quick diagnosis of a majority of nonmelanocytic disorders of the skin, hair, and nails, but it is being rightfully exploited for a plethora of nondiagnostic uses. Its use in the diagnosis of various pigmentary, papulosquamous, and infectious disorders and disorders of the scalp and hair, nails, and mucosa bears testimony to the ongoing expansion of its protean indications across skin types. Dermoscopy has transformed the conventional approach to dermatological diagnosis from clinicopathological correlation to clinico-dermoscopic-pathological correlation. It aids in convincing an otherwise reluctant patient to agree to biopsy and guides the selection of optimum site for the same. Dermoscopic clues suggestive of stability or activity of the lesion and/or disease in various dermatoses are being accrued. Early assessment of therapeutic response to treatment is helpful for physicians, patients, and researchers conducting clinical studies. Aesthetic uses of dermoscopy are opulent and being explored. Dermoscopy has also provided the much-needed balancing act of interaction between practitioners and the new generation of patients. Last but not the least, dermoscopy has resulted in patients’ better understanding of their disorders and improved compliance with treatment protocols.

Keywords : dermoscopy, trichoscopy, onychoscopy, clinico-dermoscopic correlation, dermatopathology-dermoscopic correlation, teledermoscopy

  Submitted
Jan 5, 2019
Published
Oct 31, 2019
Creative Commons License

This work is licensed under a Creative Commons Attribution 4.0 International License.

Introduction

Since the inception of dermoscopy, hitherto envisaged to evaluate suspicious nevi and noninvasively detect changes in melanocytic lesions of white-skinned individuals, the technology and its applications have come a long way. The diagnostic scope has expanded to practically every disorder of the skin and its appendages. The technology is now being rightfully exploited for its additional nondiagnostic uses [ 1 , 2 ] . Internet and social media have induced a huge change in patients’ attitude toward health care. Dermatologists are confronted with the challenge of treating a wider spectrum of patients, from the presumed highly assertive health-seeking individuals to those still consumed by archaic sociocultural beliefs. For each of these individuals, dermatologists need to deal with a different set of biases and expectations. The versatility of the dermatoscope is indeed fostering the dermatologist’s need to maintain and fine-tune the cardinal balance between the science and art of practicing dermatology.

In this review, we shall discuss the plethora of uses of dermoscopy, with special reference to the versatility of the technique including its applications beyond diagnosis.

Impact of the Publication Spree

Publications in indexed journals addressing “dermoscopy”/”dermatoscopy” have shown a constant upward trend as depicted in Table 1 . Although we employed a rather crude method for these statistics (explained in Table 1 footnotes), the figures offer a fair hint about the increase in awareness with regard to using and publishing about this technique.

Table 1

Gross Estimate of the Trend of Publications Addressing “Dermoscopy” and “Dermatoscopy”

Diagnostic Applications of Dermoscopy: Advancing and Evolving

In the past few years, this technique has been successfully explored for diagnosis of various skin, scalp, and nail disorders [ 3 ] . Subspecialties such as pigmentaroscopy, inflammoscopy (papulosquamous disorders), entodermoscopy (infections and infestations), trichoscopy (scalp and hair), onychoscopy (nails), and mucoscopy are branching out within the broad ambit of dermoscopy. Although histopathology remains the current gold standard of cutaneous diagnosis, dermoscopy and other noninvasive techniques have revolutionized the approach to diagnosis of cutaneous disorders. Dermoscopy has expanded from its original use (observation–pattern recognition–diagnosis) to other applications listed in Table 2 .

Table 2

Major Extradiagnostic Applications of Dermoscopy

Dermoscopy and Skin Biopsy

Patient Counseling, Dermoscopy-Induced Biopsy, and the Psychological Realm of the Dermatoscope: Stethoscope of the Dermatologist

Skin biopsy, despite its exigency in many situations, is sometimes refused by the patient on various premises. Facial lesions assume a special significance in this context. Despite the appearance of a biopsy-worthy and otherwise distressing lesion/pigmentation on the face, facial biopsy is often not acceptable by the patient due to concerns of potential scarring. In such commonly encountered situations, dermoscopy helps in multiple ways.

Used judiciously, dermoscopy can foster doctor-patient communication and improve patient compliance and overall management of the disorder. Demonstration of the dermoscopic image to the patient (as per the dermatologist’s discretion) and limited but tactful conversation regarding the visible features can allay the patient’s curiosity to understand the pathogenesis of his or her dermatoses. In addition, patients who warrant a skin biopsy but refuse it owing to procedure-related anxiety are more inclined to consent after having been shown the dermoscopic image with emphasis on disease-specific features. In our own experience, since we started using dermoscopy for every patient, we have observed >90% success in convincing a reluctant patient to consent to a biopsy, a concept we call “dermoscopy-induced skin biopsy” [ 1 ] . Dermoscopy can also be used to reassure a patient who fears having a condition that requires a biopsy and instead has a benign condition, eg, idiopathic guttate hypomelanosis and/or extragenital lichen sclerosus atophicus perceived as vitiligo ( Figure 1 ), or racial benign longitudinal melanonychia being dreaded to suggest subungual melanoma.

Figure 1 .

Lesions of idiopathic guttate hypomelanosis and extragenital lichen sclerosus atrophicus over the forearm of a 45-year-old woman. (A) Clinical picture of multiple discrete “confetti” hypopigmented macules over the forearm that made the patient anxious that she was suffering from vitiligo or leprosy. (B) Dermoscopy confirming the diagnosis of idiopathic guttate hypomelanosis with concomitant evolving lesions of extragenital lichen sclerosus atrophicus. Ameboid and nebuloid variants of idiopathic guttate hypomelanosis arranged in a “cloudy sky” pattern. Additionally, note the scattered white structureless areas with comedo-like plugs typical of lichen sclerosus atrophicus. Dermoscopy-guided biopsy of 2 lesions confirmed dermoscopic diagnosis. (Escope video dermatoscope, Timpac Healthcare Pvt. Ltd., New Delhi, India; ×20.) [Copyright: ©2019 Sonthalia et al.]

Finally, the dermatoscope is in essence the stethoscope of the dermatologist (vide infra). The majority of skin and hair disorders are chronic and recurring, with many being recalcitrant to treatments. Examining a lesion with a dermatoscope and discussing the images with the patient can help in the overall management of the disorder.

From Clinicopathological Correlation to Clinico-Dermoscopic-Pathological Correlation

Dermoscopists are sometimes faced with situations in which the clinicopathological diagnosis is revised after dermoscopic inputs are considered. For example, a 60-year-old, otherwise healthy man presented with a single, asymptomatic light brown plaque of 2 years’ duration over the lower abdomen. Examination revealed a solitary, oval-shaped, 3- × 4-cm, sharply demarcated annular plaque over the lower right side of the anterior abdomen that had a violaceous-to-brown central region and raised erythematous borders ( Figure 2A ). Histopathology suggested lichen planus (LP) with mild hyperkeratosis, hypergranulosis with flattening of rete ridges, Max-Joseph space formation, dense bandlike lymphohistiocytic inflammation at the dermoepidermal junction, basal cell degeneration, and colloid bodies ( Figure 2B ). However, a single lesion, atypical morphology, and lack of mucosal involvement were clinical pointers against LP. Dermoscopic evaluation revealed light brown pseudonetworks, overlapping pinkish areas, and multiple dark brown to blue-gray dots and globules ( Figure 2C ), with characteristic absence of Wickham striae. The dermoscopic features not only ruled out LP, but were characteristic of an early inflammatory lesion of LP-like keratosis [ 4 ] . Thus, an unconvincing clinicopathological diagnosis of LP was revised and confirmed to be LP-like keratosis on clinico-dermoscopic-pathological correlation. Thus, despite histopathology remaining the gold standard for diagnosis of skin disorders, cutaneous diagnosis is trending from clinicopathological correlation to clinico-dermoscopic-pathological correlation [ 1 , 2 ] . Cicatricial alopecias, especially discoid lupus erythematosus (DLE) and lichen plano pilaris, have a considerable overlap in their histology, especially in the late stage of the disease [ 5 8 ] . Appendageal loss and replacement with fibrotic tissue, vacuolar degeneration, interface dermatitis, and perifollicular infiltrate are common to both [ 6 , 7 ] . Although the inflammatory infiltrate is deeper in DLE, this feature is often insufficient for a confident diagnosis of DLE. Furthermore, the interpretation of a scalp biopsy sample is highly dependent on the site from which it is obtained. The cost and logistics of direct immunofluorescence often override the technique’s utility in differentiation of the 2 conditions. Trichoscopy dramatically simplifies this issue because classic lichen plano pilaris, scalp DLE, and frontal fibrosing alopecia have distinctive trichoscopic features [ 6 , 8 ] .

Figure 2 .

Clinico-dermoscopic-pathological correlation. (A) Single, light brown, oval-shaped annular plaque over the lower anterior abdomen. (B) Histopathology suggestive of lichen planus, revealing mild hyperkeratosis, hypergranulosis with flattening of rete ridges, Max-Joseph space formation, dense bandlike lymphohistiocytic inflammation at the dermoepidermal junction, basal cell degeneration, and colloid bodies (H&E, ×400). (C) Dermoscopy revealed light brown pseudonetworks, overlapping pinkish areas, and multiple dark brown to blue-gray dots and globules. Wickham striae were not seen. Final diagnosis of early inflammatory lesion of lichen planus-like keratosis was confirmed. (Escope video dermatoscope, Timpac Healthcare Pvt. Ltd., New Delhi, India; polarized, ×20.) [Copyright: ©2019 Sonthalia et al.]

Dermoscopy-Guided Biopsy and the Role of Ex-Vivo Dermoscopy in Histopathology Processing

The dermatopathologist’s efficiency in providing a straightforward, confident diagnosis is highly dependent on various factors from the site selection, adequacy of biopsy sample, and details filled in the pathology requisition form [ 9 ] . Dermoscopy helps in selection of the optimum site for biopsy, which increases the likelihood of a definitive histopathological diagnosis instead of reporting of nonspecific features by the pathologist. This concept of “dermoscopy-guided skin biopsy” has been reported to be advantageous in cicatricial alopecias, vasculitis, facial melanosis (eg, patient with melasma with concomitant exogenous ochronosis), collection of nail scrapings for mycological testing, and skin tumors, among others [ 10 15 ] . Dermoscopy has recently been reported to contribute further to the accuracy of histopathological diagnosis. Dermoscopy-guided histological sectioning of the biopsy tissue has been shown to optimize the sectioning of melanocytic neoplasms [ 15 ] . This principle of adapted sectioning employing ex-vivo dermoscopy may be combined with derm-dotting (marking a dermoscopically suspicious area of the specimen with nail varnish) to allow more accurate and less time-consuming histopathological diagnosis of skin tumors in a dermatopathology setting [ 16 ] .

Dermoscopy as a Diagnostic Enhancer and Tool for Monitoring Disease Activity

Defining Lesional or Disease Activity/Instability

In chronic dermatoses with a relapsing-remitting course, the disease and/or lesional activity assumes importance when a specific intervention is being considered. Prototypically, in vitiligo medical treatment remains the primary approach but surgical repigmentation is often required in later stages, for which the disease and the lesion should be “stable.” We have encountered several cases of failure of vitiligo surgery, despite the patient’s meeting the clinical criterion of stability of lack of any new lesions and/or worsening of existing lesions for at least 6 months to 2 years. Some of us (S.S., A.K.J., A.L.) have recently reported certain dermoscopic features highly suggestive of stability of vitiligo lesions that may serve as valuable adjuvant markers in qualification of the patient as a suitable candidate for surgery [ 17 , 18 ] . In our observation, perifollicular depigmentation, marginal hyperpigmentation, and presence of leukotrichia are suggestive of lesional stability ( Figure 3A ). An altered pigment pattern, perifollicular pigment retention, and certain specific features such as starburst appearance, comet tail sign, and “tapioca sago” appearance ( Figure 3B ) are suggestive of disease activity [ 17 , 18 ] . More recently, in vitiligo lesions treated surgically with micropunch grafting, we have described dermoscopic features that may serve as possibly the earliest prognostic markers of surgical outcome [ 19 ] . Another example is that of perifollicular erythema on trichoscopy as a well-established marker of active/progressive disease in frontal fibrosing alopecia [ 20 22 ] ( Figure 4 ).

Figure 3 .

Application of dermoscopy in suggesting disease activity in vitiligo. (A) A stable lesion of vitiligo fit for surgery displaying perifollicular depigmentation (black circles) and leukotrichia (blue arrow). (B) An unstable lesion displaying altered pigment network, “tapioca sago” appearance with multiple pearly-white dots (larger than eccrine openings), and micro-Köbner phenomenon (red arrows). (Escope video dermatoscope, Timpac Healthcare Pvt. Ltd., New Delhi, India; polarized, ×20.) [Copyright: ©2019 Sonthalia et al.]

Figure 4 .

Application of dermoscopy in suggesting disease activity in frontal fibrosing alopecia. (A) Clinical image of suspected frontal fibrosing alopecia in an elderly woman. (B) Dermoscopic features of multiple large white dots (fibrosed follicular ostia) with perifollicular scales and casts confirming the diagnosis and prominent perifollicular erythema suggestive of active disease. (Escope video dermatoscope, Timpac Healthcare Pvt. Ltd., New Delhi, India; polarized, ×20.) [Copyright: ©2019 Sonthalia et al.]

Defining Adequate Margins for Surgical Excision of Tumors

Akin to ex-vivo dermoscopy, which is useful for the histopathologist, in-vivo dermoscopy can add to clinical examination for the operating surgeon during surgical excision of tumors such as the basal cell carcinoma (BCC). When surgical ablation is contemplated for a BCC, excision margins between 3 and 10 mm allow for radical excision in up to 95% of cases depending on the tumor site, size, borders, and histology. In a prospective study, 200 consecutive BCCs of the head and neck were removed with 2-mm dermoscopically detected excision margins that yielded histologically confirmed complete excisions in all but 3 cases (197/200 = 98.5%) [ 23 ] . In another prospective case-control study that comprised 44 patients who underwent Mohs micrographic surgery, the group in which surgical margins were guided by dermoscopy demonstrated an outcome that was similar to that of the control group, suggesting that further research is warranted before recommending dermoscopy as an aid in demarcating surgical margins for Mohs micrographic surgery [ 24 ] .

Early Assessment of Therapeutic Response and Disease Stabilization

The conventional method of evaluation of response to treatment involves interrogating the patient about symptomatic improvement and examining the skin for the extent and morphology of lesions. It is a hard fact that clinically appreciable improvement in many chronic skin disorders, especially pigmentary dermatoses and alopecias, often requires weeks to months. This often translates into a challenging situation for the treating dermatologist with respect to making a decision on continuing or changing the treatment protocol. This also results in patient dissatisfaction, noncompliance with further therapy, and “doctor hopping.” Dermoscopy may serve as a savior in such challenging situations, as the dermoscopic improvement tends to precede clinical improvement [ 1 ] .

In alopecia areata (AA) for example, dermoscopy can confidently predict disease activity following treatment. Active AA shows black dots, “exclamation mark” or tapering hairs, broken hairs, yellow dots, and short vellus hairs ( Figure 5A ), whereas in a treatment-responsive patch of AA, black dots tend to disappear, pigtail and upright regrowing hairs appear, and yellow dots persist [ 11 , 25 27 ] ( Figure 5B ). Thus, trichoscopic review of AA patches being treated with regular intralesional steroid can help the clinician decide on the need for further sessions of intralesional steroid [ 27 ] .

Figure 5 .

Dermoscopy in evaluating treatment response with disease activity. (A) Alopecia areata patch over the beard before treatment displaying a patch of alopecia with multiple black dots (yellow arrows) and a few yellow dots, short vellus hairs (red arrows), tapering hair (blue arrow), and dystrophic hairs (white arrows). (B) An adjacent patch after 2 sessions of intralesional triamcinolone displaying hair growth, dramatic reduction of black dots, persistent yellow dots, and multiple short up-growing hairs (white arrows) suggestive of good treatment response. (Escope video dermatoscope, Timpac Healthcare Pvt. Ltd., New Delhi, India; polarized, ×20.) [Copyright: ©2019 Sonthalia et al.]

This application of dermoscopy has been documented to be useful in disorders of hyperpigmentation with either a relapsing-remitting course such as melasma [ 28 ] or a very slowly and poorly responsive course such as lichen planus pigmentosus [ 29 ] . In melasma, a recently published study as well as our own experience has shown that the presence of a prominent vascular component on dermoscopy (widened vessels) is a reliable indicator of expected improvement with vascular therapies such as pulsed-dye laser [ 30 ] and oral tranexamic acid ( Figure 6 ). Dermoscopic reevaluation of the baseline lesion(s) on the subsequent visit not only allows the clinician to appreciate posttreatment improvement (or lack thereof), but provides reassurance to the patient about the commencement of improvement, thereby maintaining treatment compliance. This use of dermoscopy is not limited to only some disorders or any particular skin type, as it has been reported from various regions and for various disorders [ 30 42 ] , a few of which are enumerated in Table 3 . Other than the evaluation of disease activity and therapeutic response, certain dermoscopic criteria (eg, pigmented structures, ulceration, and arborizing vessels in superficial BCCs treated with nonablative modalities) have been suggested to predict the presence of residual disease (residual disease-associated dermoscopic criteria) [ 43 ] .

Figure 6 .

Dermoscopy in early demonstration of treatment response in melasma. (A) Dermoscopic image from an untreated macule of melasma over the cheek of a woman displaying a diffuse nonspecific pattern of dark brown pigmentation with plentiful scattered dark brown globules and clods with perifollicular sparing and multiple prominent telangiectasias. (B) After 30 days of nightly local application of a 2% hydroquinone cream and daytime sunscreen and oral tranexamic acid (250 mg twice daily), dermoscopy from the same spot showing dramatic lightening of the background hue and erythema and reduction of pigmented structures and the telangiectasias. (Escope video dermatoscope, Timpac Healthcare Pvt. Ltd., New Delhi, India; polarized, ×20.) [Copyright: ©2019 Sonthalia et al.]

Table 3

List From Published Literature on the Use of Dermoscopy for Posttreatment Improvement Evaluation in Some Skin and Appendageal Disorders [ 30 42 ]

The aforesaid contention deepens due to the high prevalence (3%–53.6%) of dysmorphophobia or body dysmorphic disorder in patients seeking clinical dermatology consultation as well as cosmetic procedures [ 44 , 45 ] . Although psychiatric/psychological intervention constitutes their primary treatment modality, ensuring their dermatological treatment compliance is vital until their psychiatric comorbidity improves. In our experience, the majority of such patients at least acknowledge the objective improvement appreciable on dermoscopy, which reinforces treatment compliance while the psychiatric treatment continues.

Enhancing Accuracy of Reading Patch Test and Pathergy Test Results

Reading allergy patch test reactions can be challenging in the dark skin, even with a hand lens. In doubtful reactions, we have found dermoscopic imaging to be helpful in confirmation of the reaction being true positive or irritant ( Figure 7 ). Dermoscopy has also proved useful in the confirmation of pathergy test results in patients with Behçet disease [ 46 ] .

Figure 7 .

Dermoscopic aid in confirming patch test results. A grossly faint positive reaction displayed erythema and papulovesicles on dermoscopy confirming grade 2 patch test positivity. (Escope video dermatoscope, Timpac Healthcare Pvt. Ltd., New Delhi, India; polarized, ×20.) [Copyright: ©2019 Sonthalia et al.]

Therapeutic Efficacy Evaluation in Clinical Studies

The satisfaction of many clinicians with dermoscopic images serving as an early, objective, and reliable measure of pre- and posttreatment comparison has culminated in the use of dermoscopy as an important ancillary tool for efficacy evaluation of existing as well as novel therapeutic modalities in clinical studies [ 30 42 , 47 50 ] . While the avoidance of or difficulty in repeating skin biopsy (whether due to patient noncompliance or due to the posttreatment unremarkability of the lesional morphology rendering biopsy-site selection difficult) constitutes one of the important reasons for the increasing use of dermoscopy and other noninvasive imaging techniques in therapeutic efficacy evaluation in clinical studies, in studies involving both histological and dermoscopic evaluation, the objective served is the concomitant establishment and validation of dermoscopic criteria for use in future studies that may not warrant histological confirmation.

Expanding the Realm of Dermoscopy

“Cosmetic Wart Mapping”

Akin to “mole-mapping” in the white-skinned population, video dermoscopic scanning can be useful for mapping of multiple cosmetic pigmented warts (usually verruca plana [VP]) in dark-skinned patients, particularly involving the beard area in men and periorbital area in women. Cosmetic warts arise from a single or few verrucae over the face due to pseudoköbnerization induced by temporary hair removal methods such as shaving, threading, and waxing [ 51 ] . Men with multiple VP of the beard region or women with VP involving the threading-treated areas around the eyebrows can be provided with ablation of many more lesions if video dermoscopy is used to scan the affected area compared to the conventional ablation of lesions visible to the unaided eye ( Figure 8 ). If left untreated, these tiny lesions invisible to the eye and hand lens might contribute to further dissemination [ 1 , 2 , 28 ] .

Figure 8 .

Dermoscopy for cosmetic wart mapping in darker skin. (A) Linear köbnerized cluster of verruca barbae in an Indian man before ablation. (B) Dermoscopy done after radiofrequency ablation of the warts (erosions) revealing at least 2 warts (black arrows) missed despite using magnifying surgical loupes during the procedure. (Escope video dermatoscope, Timpac Healthcare Pvt. Ltd., New Delhi, India; polarized, ×20.) [Copyright: ©2019 Sonthalia et al.]

Aesthetic Applications of Dermoscopy

Dermoscopy also finds its utility in certain cosmetic/aesthetic procedures. A dermoscopic photo-aging scale has been recently conceived and found to be a reliable and valid diagnostic tool for quantitative evaluation of photo-aged facial skin in a white population and to study the effect of preventive and therapeutic approaches to skin aging in the future [ 52 ] . Dermoscopic evaluation of periocular hyperpigmentation and under-eye bags can provide a clue to the predominant abnormality (skin pigmentation, abnormal vasculature, skin laxity) ( Figure 9 ) and aid in development of customized treatment protocols. In a recent study evaluating the impact of normobaric oxygen therapy on periorbital darkening, dermoscopy was used as the main tool to document posttherapy improvement and revealed a substantial reduction in vascularity and pigmentation with more than a quarter of patients showing >50% improvement [ 53 ] .

Figure 9 .

Dermoscopy of the under-eye region for management of periocular pigmentation. (A) Predominantly pigmentary component; (B) predominantly vascular component; and (C) combination of pigmentary and vascular component. (DermLite DL4, 3 Gen Inc., USA; polarized, ×10.) [Copyright: ©2019 Sonthalia et al.]

Enlarged facial skin pores is a common cosmetic complaint, especially in individuals with oily skin. Dermoscopy can aid in evaluating and defining “enlarged” open facial pores [ 54 ] . Kim et al have defined and categorized the morphological subtypes of skin pores into 3 different categories: “visible skin pores” (0.1–0.6 mm 2 ), “enlarged skin pores” (0.3–0.6 mm 2 ), and “blackhead embedded skin pores” using the Robo Skin Analyzer CS50 (NIIC, Tokyo, Japan), which has a dermatoscope-like attachment mode in addition to other functions [ 55 ] . Figure 10 provides a gross idea of types of pores on a standard dermoscopic evaluation.

Figure 10 .

Dermoscopy of skin pores. Well-defined pilosebaceous openings or pores visible on dermoscopy of the cheek of an Indian woman with enlarged open pores. Note the presence of visible skin pores (black arrows), enlarged skin pores (blue arrows), and blackhead-embedded skin pores (white arrows). (Escope video dermatoscope, Timpac Healthcare Pvt. Ltd., New Delhi, India; polarized, ×20.) [Copyright: ©2019 Sonthalia et al.]

Selecting the right parameters while using devices for laser hair reduction is not only crucial for optimum outcome and patient satisfaction, it is critical to prevent laser-induced burn and postprocedure hyperpigmentation in dark-skinned individuals (Fitzpatrick skin photo types IV–VI). In our own experience, dermoscopic evaluation of the scattering and thickness of hairs before the laser session has proven useful in dark-skinned patients with hirsutism. Optimal laser parameters (especially pulse duration that depends on the thickness of the hair being targeted) can thus be correspondingly fine-tuned. Moreover, apprehensive patients can be shown the laser-induced scattering and thinning of hirsute hairs to maintain or improve compliance ( Figure 11 ). In fact, a recent study has emphasized the utility of trichoscopy in monitoring the response to laser hair reduction in women [ 56 ] .

Figure 11 .

Dermoscopy for deciding laser/light device and parameters for permanent hair reduction. (A) Dermoscopy of the chin of an obese woman with polycystic ovarian syndrome revealing thick terminal hairs and darkly pigmented skin. (B) Image from the same patient after 8 sessions of diode laser (with low energy) showing dramatic scattering and thinning of chin hairs. (Escope video dermatoscope, Timpac Healthcare Pvt. Ltd., New Delhi, India; polarized, ×20.) [Copyright: ©2019 Sonthalia et al.]

Trichoscopy is of great value to a hair transplant surgeon. It aids in recording the number of existing follicular units, the number of hairs per follicular unit, the size of hair follicles, as well as the interfollicular distance at both the donor and recipient site. In addition, trichoscopy may be useful for early differential diagnosis of posttransplant surgical complications such as folliculitis and secondary lichen planopilaris. A detailed account of clinco-trichoscopic correlation in the scalp of patients who underwent hair transplantation has been documented by Madura et al [ 57 ] .

Detection of Intra/Subcutaneous Foreign Bodies and Retained Sutures

The detection and removal of retained sutures in a crusted wound may sometimes become daunting, especially when black threads (typically silk) are used in individuals with darker skin due to the relative lack of color contrast compared with fair skin. In such situations, dermoscopic assessment provides an excellent 3-dimensional view that may facilitate their prompt identification and removal ( Figure 12 ) [ 28 ] . A blue Prolene suture should help in avoiding this issue in all skin types, although dermoscopy may still help in visualizing the ends of the residual suture if stitch removal is done incorrectly. Dermoscopy has also been documented for its application in facilitating identification and removal of a foreign body lodged in the skin ( Figure 13 ) [ 28 , 58 ] .

Figure 12 .

Dermoscopy for identification and removal of retained sutures in a heavily crusted wound. (A) Before removal, the black suture, which was otherwise extremely difficult to delineate from the surrounding brownish black crust, is easily visible on dermoscopy (white circle). (B) After removal. (Escope video dermatoscope, Timpac Healthcare Pvt. Ltd., New Delhi, India; polarized, ×20.) [Copyright: ©2019 Sonthalia et al.]

Figure 13 .

Dermoscopy for identification and removal of intracutaneous foreign body. (A) Clinical image before removal—the tiny foreign body lodged intracutaneously (black arrow) with no visibility of protruding head or tail for removal. (B) Low magnification (×20) polarized dermoscopic image. (C) High magnification (×70) polarized dermoscopic image revealing the protruding head-end of the foreign body. (Escope video dermatoscope, Timpac Healthcare Pvt. Ltd., New Delhi, India; polarized, ×20.) (D) Clinical image after dermoscopically facilitated removal revealing a tiny linear subcorneal erosion (black arrow). [Copyright: ©2019 Sonthalia et al.]

Teledermoscopy

Teledermatology is a subspecialty of dermatology that uses telecommunication technologies to transfer medical information over varying distances. The format can be audio, visual, and/or data-based. Digital dermoscopy refers to the acquisition and storage of digital images from a dermoscopic examination. Teledermoscopy is the transferring of a digitalized dermoscopic image (visual data) for diagnosis ( Figure 14 ), education, consultation, or follow-up. Mobile teledermoscopy uses a smartphone to deliver the same type of service [ 59 ] . These images are also used in machine learning [ 60 , 61 ] , a rapidly developing area that will soon change our way of seeing and understanding a new device or medication.

Figure 14 .

Dermoscopic image received via teledermatology consultation with a family physician. The patient was referred directly to surgery, and the diagnosis of melanoma was confirmed by pathology. (DermLite DL4, 3 Gen Inc., USA; polarized, ×10.) [Copyright: ©2019 Sonthalia et al.]

Teledermoscopy’s greatest strength may be as a triage and monitoring tool, as it can reduce the number of unnecessary referrals, wait times, and the cost of providing and receiving dermatological care [ 61 ] . Inclusion of dermoscopic images in teledermatology-based consultations is known to improve decisions on triaging and surgical excision of melanomas and other skin cancers [ 59 ] . The concept of teledermoscopy has futuristic implications for health care systems in the developing world [ 61 ] , where a large proportion of dermatology patients are still managed by primary care physicians [ 62 ] . Of course, this goal can be successfully achieved only with proper training into dermoscopy and principles of teledermoscopy of both primary care physicians and dermatologists.

Psychological Realm of Dermoscopy

Dermoscopy: The Dermatologist’s Tool in the Era of Social Media Empowerment of Patients

In the current era, the practice of medicine and specifically dermatology is facing a new challenge. Over and above the chronicity and relapsing nature of the majority of cutaneous disorders, the impact of health-related information available on the internet and exchanged on social media has dramatically altered the approach to practicing dermatology [ 63 ] . While a detailed discussion on the impact of social media on the practice of dermatology is beyond the scope of this article, it may suffice to mention that the above concerns make a strong point favoring the concept of “e-professionalism” as a distinct new paradigm requiring particular training, practice, and formulation of new policies that prescribe guidelines for normative behavior to regulate and reduce social media use in dermatology [ 64 ] . Pending global and regional consensus guidelines on regulating the use of social media in health care, dermoscopy may serve as an efficient tool for counteracting the invalid and illogical interjections of the “google generation” patients in the diagnostic and therapeutic decisions made by dermatologists.

Dermatoscope: A Professional Highlight for Dermatologists

While a hand lens, corneal loupe, and other conventional tools of magnification are present in nearly every dermatologist’s office, a dermatoscope definitely adds to the professional standing. Patients tend to place more faith in a dermatologist who is well-versed in dermoscopy and uses it not just for making diagnoses, but also to counsel them on pertinent features appreciable on dermoscopy that are of relevance to their understanding and improved therapeutic compliance.

Dermatoscope: The Dermatologist’s Stethoscope

Cutaneous disorders are often chronic, treatment-recalcitrant, and with an unpredictable/relapsing-remitting course. Patients with conditions such as psoriasis, vitiligo, nonremitting AA, and chronic eczemas typically consult different dermatologists over time, hoping for a permanent cure. Chronic skin diseases may have a devastating effect on a person’s physical and psychological well-being, affecting his or her education, relationships, career choices, social and leisure activities, and sex life. The adverse physical, psychological, and social consequences of chronic dermatoses affect not only the patient, but also caregivers and family members [ 65 ] . Demonstration of dermoscopic images (in select cases) to the patient and/or relatives tends to improve the patient’s psychodermatology profile and provides reassurance to caregivers [ 1 , 2 ] . The relation between a patient’s psychological well-being and response to therapy need not be overemphasized. Dermoscopic examination and counseling thereof tend to make such patients and family members feel they are being cared for.

Future Perspective

Innovations in the technique and utilization of dermoscopy for better imaging and expanding its extradiagnostic application are being conceived and published at a fast pace. One such newfangled approach is dermoscopy-guided dark-field multifunctional optical coherence tomography, conceptualized and developed by Kwon et al [ 66 ] . By combining the 2 imaging techniques, Kwon et al achieved simultaneous high-contrast superficial information (dermoscopy) and depth-resolved structural, birefringent, and vascular information of the skin (multifunctional optical coherence tomography) and documented its utility in better overall evaluation of different skin lesions.

Akin to endoscopic procedures in surgical branches, we believe that the dermatoscope may be amenable to redesigning with creation of multiple portals for diagnostic and therapeutic interventions [ 67 ] delivered through the device to allow high-precision diagnostic and dermatosurgical procedures under concomitant dermoscopic visualization.

Conclusions

Dermoscopy has far-reaching uses beyond just diagnosis of skin, hair, and nail disorders. Some can be highly relevant for both physicians and patients, offering prompt resolution to diagnostic and therapeutic dilemmas encountered routinely. The quest for more uses of this technique continues and mastering this technology becomes imperative for not only dermatologists, but also primary care physicians, pediatricians, and specialists of other branches of medicine.

References

  1. Dermoscopy—not just for diagnosis and not just for dermatologists! Sonthalia S, Errichetti E. Kathmandu Univ Med J (KUMJ).2017;15(1):1-2.
  2. Dermoscopy Overview and Extradiagnostic Applications. [Updated 2019 Jan 20] Sonthalia S, Kaliyadan F. StatPearls [Internet].2019 Jan–2019 May.
  3. Dermoscopy in general dermatology: a practical overview Errichetti E, Stinco G. Dermatol Ther (Heidelb).2016;6(4):471-507.
  4. Chronology of lichen planus-like keratosis features by dermoscopy: a summary of 17 cases Watanabe S, Sawada M, Dekio I, Ishizaki S, Fujibayashi M, Tanaka M. Dermatol Pract Concept.2016;6(2):29-35.
  5. Primary cicatricial alopecia: histopathologic findings do not distinguish clinical variants Mirmirani P, Willey A, Headington JT, Stenn K, McCalmont TH, Price VH. J Am Acad Dermatol.2005;52(4):637-643.
  6. Clinical, trichoscopic, and histopathological features of primary cicatricial alopecias: a retrospective observational study at a tertiary care centre of North East India Thakur BK, Verma S, Raphael V. Int J Trichology.2015;7(3):107-112.
  7. Lichen planopilaris versus discoid lupus erythematosus: a trichoscopic perspective Ankad BS, Beergouder SL, Moodalgiri VM. Int J Trichology.2013;5(4):204-207.
  8. Lichen planopilaris and frontal fibrosing alopecia cannot be differentiated by histopathology Gálvez-Canseco A, Sperling L. J Cutan Pathol.2018;45(5):313-317.
  9. Practical strategies to improve the clinical utility of the dermatopathology report Trotter MJ, Au S, Naert KA. Arch Pathol Lab Med.2016;140(8):759-765.
  10. Dermoscopy guided scalp biopsy in cicatricial alopecia Miteva M, Tosti A. J Eur Acad Dermatol Venereol.2013;27(10):1299-1303.
  11. Scalp dermoscopy or trichoscopy Lacarrubba F, Micali G, Tosti A. Curr Probl Dermatol.2015;47:21-32.
  12. Exogenous ochronosis in a Chinese patient: use of dermoscopy aids early diagnosis and selection of biopsy site Liu WC, Tey HL, Lee JS, Goh BK. Singapore Med J.2014;55(1):e1-e3.
  13. Blue-gray blotch: a helpful dermoscopic finding in optimal biopsy site selection for true vasculitis Choo JY, Bae JM, Lee JH, Lee JY, Park YM. J Am Acad Dermatol.2016;75(4):836-838.
  14. Dermoscopy and onychomycosis: guided nail abrasion for mycological samples Bet DL, Reis AL, Di Chiacchio N, Belda W. An Bras Dermatol.2015;90(6):904-906.
  15. The utility of dermoscopy-guided histologic sectioning for the diagnosis of melanocytic lesions: a case-control study Merkel EA, Amin SM, Lee CY, et al. J Am Acad Dermatol.2016;74(6):1107-1113.
  16. Pathologic evaluation of skin tumors with ex vivo dermoscopy with derm dotting Haspeslagh M, Hoorens I, Degryse N, et al. JAMA Dermatol.2017;153(2):154-161.
  17. Dermoscopy in vitiligo: diagnosis and beyond Jha AK, Sonthalia S, Lallas A, Chaudhary RKP. Int J Dermatol.2018;57(1):50-54.
  18. Dermoscopy as an evolving tool to assess vitiligo activity Jha AK, Sonthalia S, Lallas A. J Am Acad Dermatol.2018;78(5):1017-1019.
  19. Post-graft trichrome and Manchurian gravy signs on dermoscopy can predict disease activity in vitiligo lesions post-skin grafting Jha AK, Sonthalia S, Lallas A, Chaudhary RKP. Int J Dermatol.2018;57(11):e144-e145.
  20. Perifollicular erythema as a trichoscopy sign of progression in frontal fibrosing alopecia Toledo-Pastrana T, Hernández MJ, Camacho Martínez FM. Int J Trichology.2013;5(3):151-153.
  21. Thermal imaging and dermoscopy for detecting inflammation in frontal fibrosing alopecia Lis-Święty A, Miziołek B, Ranosz-Janicka I, Bierzyńska-Macyszyn G, Brzezińska-Wcisło L. J Cosmet Dermatol.2018;17(2):268-273.
  22. A dermoscopic diagnosis and activity evaluation of frontal fibrosing alopecia in an Indian lady Sonthalia S, Jha AK, Tiwary PK. Indian Dermatol Online J.2017;8(2):162-163.
  23. Dermoscopy-guided surgery in basal cell carcinoma Caresana G, Giardini R. J Eur Acad Dermatol Venereol.2010;24(12):1395-1399.
  24. Utility of dermoscopy for demarcation of surgical margins in Mohs micrographic surgery Suzuki HS, Serafini SZ, Sato MS. An Bras Dermatol.2014;89(1):38-43.
  25. Trichoscopy in alopecias: diagnosis simplified Jain N, Doshi B, Khopkar U. Int J Trichology.2013;5(4):170-178.
  26. Trichoscopic findings in alopecia areata and their relation to disease activity, severity and clinical subtype in Turkish patients Kibar M, Aktan Ş, Lebe B, Bilgin M. Australas J Dermatol.2015;56(1):e1-e6.
  27. Dermoscopic evaluation of therapeutic response to an intralesional corticosteroid in the treatment of alopecia areata Ganjoo S, Thappa DM. Indian J Dermatol Venereol Leprol.2013;79(3):408-417.
  28. Monitoring of therapeutic response and other applications Sonthalia S, Kaur T, Srivastava S, Lallas A, Errichetti E, Ioannides D. Dermoscopy in General Dermatology.2018;:325-329.
  29. Modified phenol peels for treatment-refractory hyperpigmentation of lichen planus pigmentosus: a retrospective clinico-dermoscopic analysis Sonthalia S, Vedamurthy M, Thomas M, et al. J Cosmet Dermatol..
  30. Treatment of melasma with pulsed-dye laser and1,064-nm Q-switched Nd:YAG laser: a split-face study Kong SH, Suh HS, Choi YS. Ann Dermatol.2018;30(1):1-7.
  31. Efficacy of ingenol mebutate in the treatment of actinic keratoses: a pre- and posttreatment dermoscopic comparative analysis Carbotti M, Coppola R, Zanframundo S, Devirgiliis V, Panasiti V. Biomed Res Int.2018;2018.
  32. A novel topical agent in the treatment of seborrheic keratoses: a proof of concept study by clinical and dermoscopic evaluation Lacarrubba F, Nasca MR, Verzì AE, Micali G. Dermatol Ther.2017;30(5):e12526.
  33. Platelet-rich plasma with microneedling in androgenetic alopecia along with dermoscopic pre- and post-treatment evaluation Jha AK, Udayan UK, Roy PK, Amar AKJ, Chaudhary RKP. J Cosmet Dermatol.2018;17(3):313-318.
  34. Dermatoscopy-guided therapy of pigmented basal cell carcinoma with imiquimod Husein-ElAhmed H, Fernandez-Pugnaire MA. An Bras Dermatol.2016;91(6):764-769.
  35. Dermoscopic hemorrhagic dots: an early predictor of response of psoriasis to biologic agents Lallas A, Argenziano G, Zalaudek I, et al. Dermatol Pract Concept.2016;6(4):7-12.
  36. Carbon dioxide laser versus erbium: YAG laser in treatment of epidermal verrucous nevus: a comparative randomized clinical study Osman MAR, Kassab AN. J Dermatolog Treat.2017;28(5):452-457.
  37. The use of dermatoscopy to monitor therapeutic response of Bowen disease: a dermatoscopic pathological study Mun JH, Park JM, Song M, et al. Br J Dermatol.2012;167(6):1382-1385.
  38. Combining topical tretinoin with mometasone furoate in the treatment of vulvar lichen sclerosus: results of dermoscopic assessment Corazza M, Maietti E, Toni G, Virgili A, Borghi A. Dermatol Ther.2018;31(6):e12735.
  39. Utility of dermoscopy for evaluating the therapeutic efficacy of tacrolimus ointment plus 308-nm excimer laser combination therapy in localized vitiligo patients Wang LM, Lu WJ, Yuan JT, et al. Exp Ther Med.2018;15(4):3981-3988.
  40. Comparison of the effect of diode laser versus intense pulsed light in axillary hair removal Ormiga P, Ishida CE, Boechat A, Ramos-E-Silva M. Dermatol Surg.2014;40(10):1061-1069.
  41. A comparison of intense pulsed light and laser treatment of telangiectases in patients with systemic sclerosis: a within-subject randomized trial Dinsdale G, Murray A, Moore T, et al. Rheumatology (Oxford).2014;53(8):1422-1430.
  42. Videodermatoscopy enhances the ability to monitor efficacy of scabies treatment and allows optimal timing of drug application Micali G, Lacarrubba F, Tedeschi A. J Eur Acad Dermatol Venereol.2004;18(2):153-154.
  43. Applicability of dermoscopy for evaluation of patients’ response to nonablative therapies for the treatment of superficial basal cell carcinoma Apalla Z, Lallas A, Tzellos T, et al. Br J Dermatol.2014;170(4):809-815.
  44. Body dysmorphic disorder in the dermatology patient Koblenzer CS. Clin Dermatol.2017;35(3):298-301.
  45. Body dysmorphic disorder in the cosmetic practice Kuhn H, Cunha PR, Matthews NH, Kroumpouzos G. G Ital Dermatol Venereol.2018;153(4):506-515.
  46. The dermatoscopy in the skin pathergy testing: case series in patients with suspected Behçet’s disease [in Portuguese] Scherrer MA, de Castro LP, Rocha VB, Pacheco L. Rev Bras Reumatol.2014;54(6):494-498.
  47. Treatment of erythemato-telangiectatic rosacea with brimonidine alone or combined with vascular laser based on preliminary instrumental evaluation of the vascular component Micali G, Dall’Oglio F, Verzì AE, Luppino I, Bhatt K, Lacarrubba F. Lasers Med Sci.2018;33(6):1397-1400.
  48. Enhancing hair growth in male androgenetic alopecia by a combination of fractional CO 2 laser therapy and hair growth factors Huang Y, Zhuo F, Li L. Lasers Med Sci.2017;32(8):1711-1718.
  49. Efficacy and tolerability of a spray product containing hydroxypropyl chitosan, climbazole and piroctone olamine, applied twice weekly for the treatment of the pitiriasis versicolor Fabbrocini G, Panariello L, DE Padova MP, et al. G Ital Dermatol Venereol.2017;152(6):565-568.
  50. Effects of topical application of B-resorcinol and glycyrrhetinic acid monotherapy and in combination with fractional CO 2 laser treatment for benign hand hyperpigmentation treatment Grippaudo FR, Di Russo PP. J Cosmet Dermatol.2016;15(4):413-419.
  51. Cosmetic warts: pseudo-koebnerization of warts after cosmetic procedures for hair removal Sidharth S, Rahul A, Rashmi S. J Clin Aesthet Dermatol.2015;8(7):52-56.
  52. Development of skin aging scale by using dermoscopy Isik B, Gurel MS, Erdemir AT, Kesmezacar O. Skin Res Technol.2013;19(2):69-74.
  53. The effects of normobaric oxygen therapy on patients with periorbital darkening: an open, uncontrolled trial Mostafa WZ, Kadry DM, Mohamed EF. Indian J Dermatol Venereol Leprol.2015;81(4):427-429.
  54. The conundrum of skin pores in dermocosmetology Uhoda E, Piérard-Franchimont C, Petit L, Piérard GE. Dermatology.2005;210(1):3-7.
  55. Sebum, acne, skin elasticity, and gender difference—which is the major influencing factor for facial pores? Kim BY, Choi JW, Park KC, Youn SW. Skin Res Technol.2013;19(1):e45-53.
  56. Trichoscopic changes in hair during treatment of hirsutism with 1064-nm neodymium:yttrium-aluminum-garnet laser Mohamed EE, Ahmed AM, Tawfik KM, Ibrahim SM. J Cosmet Dermatol.2016;15(1):31-35.
  57. Clinical and trichoscopic correlation in scalp of patients who had undergone hair transplantation Madura C, Ravipati N, Chandrashekhar BS. International Journal of Dermoscopy.2017;1(1):20-25.
  58. Dermoscopy for the detection and safe extraction of an intracutaneous foreign body Sonthalia S, Jha AK, Kaliyadan F. J Am Acad Dermatol.2018;79(2):e19-e20.
  59. Recent trends in teledermatology and teledermoscopy Lee KJ, Finnane A, Soyer HP. Dermatol Pract Concept.2018;8(3):214-223.
  60. Going digital with dermoscopy Bleicher B, Levine A, Markowitz O. Cutis.2018;102(2):102-105.
  61. Teledermatology and its current perspective Pasquali P, Sonthalia S, Moreno DR, et al. Indian Dermatol Online J..
  62. Antifungal therapeutic failures in India: an important issue being overlooked Sonthalia S, Agrawal M, Goldust M, Das S, Bhattacharya SN. Lancet Infect Dis.2018;18(11):1181-1182.
  63. Role of social media in clinical practice: legal implications Sonthalia S, Arora D, Sharma A, Mhatre M, Mysore M, Bhat S, Sirur SP. Medicolegal Aspects of Dermatology & Plastic Surgery.2019;:193-222.
  64. E-professionalism: a new paradigm for a digital age Cain J, Romanelli F. Curr Pharm Teach Learn.2009;1(2):66-70.
  65. Psychiatric and psychological impact of chronic skin disease Jafferany M, Pastolero P. Prim Care Companion CNS Disord.2018;20(2).
  66. Dermoscopy guided dark-field multi-functional optical coherence tomography Kwon S, Yoon Y, Kim B, et al. Biomed Opt Express.2017;8(3):1372-1381.
  67. Interventional Dermoscopy Sonthalia S, Khurana R. J Am Acad Dermatol.2019. CrossRef

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