Digital Dermoscopy Analysis in the Diagnosis of Acral and Nail Melanocytic Tumors
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Acral Compound Nevus SJ Yun S Korea
University of Pennsylvania, Founded by Ben Franklin in 1740 Disclosures Consultant for Myriad Genetics and for SciBase (might try to sell you a book, as well) Multidimensional Pathway Classification of Melanocytic Tumors WHO 4th Edition, 2018 Epidemiologic, Clinical, Histologic and Genomic Aspects of Melanoma David E. Elder, MB ChB, FRCPA University of Pennsylvania, Philadelphia, PA, USA Napa, May, 2018 3rd Edition, 2006 Malignant Melanoma • A malignant tumor of melanocytes • Not all melanomas are the same – variation in: – Epidemiology – risk factors, populations – Cell/Site of origin – Precursors – Clinical morphology – Microscopic morphology – Simulants – Genomic abnormalities Incidence of Melanoma D.M. Parkin et al. CSD/Site-Related Classification • Bastian’s CSD/Site-Related Classification (Taxonomy) of Melanoma – “The guiding principles for distinguishing taxa are genetic alterations that arise early during progression; clinical or histologic features of the primary tumor; characteristics of the host, such as age of onset, ethnicity, and skin type; and the role of environmental factors such as UV radiation.” Bastian 2015 Epithelium associated Site High UV Low UV Glabrous Mucosa Benign Acquired Spitz nevus nevus Atypical Dysplastic Spitz Borderline nevus tumor High Desmopl. Low-CSD Spitzoid Acral Mucosal Malignant CSD melanoma melanoma melanoma melanoma melanoma 105 Point mutations 103 Structural Rearrangements 2018 WHO Classification of Melanoma • Integrates Epidemiologic, Genomic, Clinical and Histopathologic Features • Assists -
Optimal Management of Common Acquired Melanocytic Nevi (Moles): Current Perspectives
Clinical, Cosmetic and Investigational Dermatology Dovepress open access to scientific and medical research Open Access Full Text Article REVIEW Optimal management of common acquired melanocytic nevi (moles): current perspectives Kabir Sardana Abstract: Although common acquired melanocytic nevi are largely benign, they are probably Payal Chakravarty one of the most common indications for cosmetic surgery encountered by dermatologists. With Khushbu Goel recent advances, noninvasive tools can largely determine the potential for malignancy, although they cannot supplant histology. Although surgical shave excision with its myriad modifications Department of Dermatology and STD, Maulana Azad Medical College and has been in vogue for decades, the lack of an adequate histological sample, the largely blind Lok Nayak Hospital, New Delhi, Delhi, nature of the procedure, and the possibility of recurrence are persisting issues. Pigment-specific India lasers were initially used in the Q-switched mode, which was based on the thermal relaxation time of the melanocyte (size 7 µm; 1 µsec), which is not the primary target in melanocytic nevus. The cluster of nevus cells (100 µm) probably lends itself to treatment with a millisecond laser rather than a nanosecond laser. Thus, normal mode pigment-specific lasers and pulsed ablative lasers (CO2/erbium [Er]:yttrium aluminum garnet [YAG]) are more suited to treat acquired melanocytic nevi. The complexities of treating this disorder can be overcome by following a structured approach by using lasers that achieve the appropriate depth to treat the three subtypes of nevi: junctional, compound, and dermal. Thus, junctional nevi respond to Q-switched/normal mode pigment lasers, where for the compound and dermal nevi, pulsed ablative laser (CO2/ Er:YAG) may be needed. -
Pigmented Vulvar Lesions. Dermatoscopy. Is It Advisable?
"ISSVD - International Society for the Study of Vulvovaginal Disease " PIGMENTED VULVAR LESIONS. DERMATOSCOPY. IS IT ADVISABLE? Damian Ferrario MD. Dermatology Department. Italian Hospital of Buenos Aires Without Conflic Interest PIGMENTED VULVAR LESIONS • Pigmented skin lesions in the vulvar area include nevi, melanoma, melanotic macules (lentiginosis, melanosis), angiokeratomas, seborrheic keratosis, SeborrHeic keratosis AMNGT squamous cell carcinoma, basal cell carcinoma (BCC). • Atypical melanocytic nevi of the genital type (AMNGT) and vulvar melanomas usually affect postmenopausal women and the prognosis is poor. Melanosis Melanoma Pigmented lesions of the vulva are present in 20% of the women who Have Had gynecological examination. Even thougH vulvar pigmented lesions Has a benign prognosis, it causes concern to the patient and to the pHysician, owing to its melanoma-liKe presentation. Vulvar melanosis is the most frequent lesion among these pigmented disorders... but COLPOSCOPY You examine a 40-year-old patient and detect a nevus in the upper labia majora. According to Her, she Has it since childHood. She does not remember whether it grew or not. It is asymptomatic. WHAT IS YOUR BEHAVIOR? A. Do nothing and continue the examination. B. Urgently refer the patient to a dermatologist telling her it may be a melanoma. C. Performing radical You examine a 40-year-old patient and detect a nevus in the region of the labia surgery for suspected majora. According to Her, she Has it since childHood. He does not remember melanoma. whether He grew up. It is asymptomatic. D. Take a biopsy. A. Do nothing and continue the examination. B. Urgently refer the patient to a dermatologist telling her it may be a melanoma. -
Acral Melanoma
Accepted Date : 07-Jul-2015 Article type : Original Article The BRAAFF checklist: a new dermoscopic algorithm for diagnosing acral melanoma Running head: Dermoscopy of acral melanoma Word count: 3138, Tables: 6, Figures: 6 A. Lallas,1 A. Kyrgidis,1 H. Koga,2 E. Moscarella,1 P. Tschandl,3 Z. Apalla,4 A. Di Stefani,5 D. Ioannides,2 H. Kittler,4 K. Kobayashi,6,7 E. Lazaridou,2 C. Longo,1 A. Phan,8 T. Saida,3 M. Tanaka,6 L. Thomas,8 I. Zalaudek,9 G. Argenziano.10 Article 1. Skin Cancer Unit, Arcispedale Santa Maria Nuova IRCCS, Reggio Emilia, Italy 2. Department of Dermatology, Shinshu University School of Medicine, Matsumoto, Japan 3. Department of Dermatology, Division of General Dermatology, Medical University, Vienna, Austria 4. First Department of Dermatology, Medical School, Aristotle University, Thessaloniki, Greece 5. Division of Dermatology, Complesso Integrato Columbus, Rome, Italy 6. Department of Dermatology, Tokyo Women’s Medical University Medical Center East, Tokyo, Japan 7. Kobayashi Clinic, Tokyo, Japan 8. Department of Dermatology, Claude Bernard - Lyon 1 University, Centre Hospitalier Lyon-Sud, Pierre Bénite, France. 9. Department of Dermatology and Venereology, Medical University, Graz, Austria 10. Dermatology Unit, Second University of Naples, Naples, Italy. This article has been accepted for publication and undergone full peer review but has not been through the copyediting, typesetting, pagination and proofreading process, which may lead to differences between this version and the Version of Record. Please cite this article as Accepted doi: 10.1111/bjd.14045 This article is protected by copyright. All rights reserved. Please address all correspondence to: Aimilios Lallas, MD. -
Acral Lentiginous Melanoma in Situ: Dermoscopic Features and Management Strategy Byeol Han1,2, Keunyoung Hur1, Jungyoon Ohn1,2, Sophie Soyeon Lim3 & Je‑Ho Mun1,2*
www.nature.com/scientificreports OPEN Acral lentiginous melanoma in situ: dermoscopic features and management strategy Byeol Han1,2, Keunyoung Hur1, Jungyoon Ohn1,2, Sophie Soyeon Lim3 & Je‑Ho Mun1,2* Diagnosis of acral lentiginous melanoma in situ (ALMIS) is challenging. However, data regarding ALMIS are limited in the literature. The aim of this study was to investigate the clinical and dermoscopic features of ALMIS on palmoplantar surfaces. Patients with ALMIS and available dermoscopic images were retrospectively reviewed at our institution between January 2013 and February 2020. Clinical and dermoscopic features were analysed and compared between small (< 15 mm) and large (≥ 15 mm) ALMIS. Twenty‑one patients with ALMIS were included in this study. Mean patient age was 58.5 (range 39–76) years; most lesions were located on the sole (90.5%). The mean maximal diameter was 19.9 ± 13.7 mm (mean ± standard deviation). Statistical analysis of dermoscopic features revealed that parallel ridge patterns (54.5% vs. 100%, P = 0.035), irregular difuse pigmentation (27.3% vs. 100%, P = 0.001) and grey colour (18.2% vs. 90%, P = 0.002) were signifcantly less frequent in small lesions than in large lesions. We have also illustrated two unique cases of small ALMIS; their evolution and follow‑up dermoscopic examination are provided. In conclusion, this study described detailed dermoscopic fndings of ALMIS. Based on the present study and a review of the literature, we proposed a dermoscopic algorithm for the diagnosis of ALMIS. Acral lentiginous melanoma (ALM), frst described by Reed in 1976, is a histological subtype of cutaneous melanoma arising on the acral areas1,2. -
Dermoscopy—The Ultimate Tool for Melanoma Diagnosis
Dermoscopy—The Ultimate Tool for Melanoma Diagnosis Giuseppe Argenziano, MD,* Gerardo Ferrara, MD,† Sabrina Francione, MD,* Karin Di Nola, MD,* Antonia Martino, MD,* and Iris Zalaudek, MD‡ “We are beginning to move away from clinicopathologic diagnosis into an era of clinico- imaging diagnosis.” This vision became a fact, as the dermatoscope represents nowadays the dermatologist stethoscope. This is not only because dermoscopy reveals a new and fascinating morphologic dimension of pigmented and nonpigmented skin tumors, but also because it improves the recognition of a growing number of skin symptoms in general dermatology. Melanoma detection remains the most important indication of dermoscopy and in melanoma screening the aim of dermoscopy is to maximize early detection while minimizing the unnecessary excision of benign skin tumors. In the last few years, 3 meta-analyses and 2 randomized studies have definitely proven that dermoscopy allows improving sensitivity for melanoma as compared to the naked eye examination alone. This is the consequence of at least 3 issues: first, the presence of early dermoscopy signs that are visible in melanoma much before the appearance of the classical clinical features; second, an increased attitude of clinicians to check more closely clinically banal-looking lesions; third, an improved attitude of clinicians to monitor their patients. Semin Cutan Med Surg 28:142-148 © 2009 Elsevier Inc. All rights reserved. The Dermatologist Stethoscope dots” pattern in psoriasis and the “whitish striae” pattern in lichen planus.15-20 In a recent review of the indications in “ e are beginning to move away from clinicopathologic dermoscopy, more than 35 different inflammatory and infec- 1 Wdiagnosis into an era of clinicoimaging diagnosis.” tious skin diseases have been listed.21 As reported in several This is what Robinson and Callen wrote in 2005, a vision case series, one of the newest applications is represented by that, to our estimation, is slowly becoming true. -
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ORIGINAL ARTICLE Magdalena Chrabąszcz1 , Cezary Maciejewski2 , Teresa Wolniewicz1, Rosanna Alda-Malicka1, Patrycja Gajda1, Joanna Czuwara1 , Lidia Rudnicka1 1Department of Dermatology, Medical University of Warsaw, Poland 21st Department of Cardiology, Medical University of Warsaw, Poland Access to a dermatoscope during dermatology courses motivates students’ towards thorough skin examination Address for correspondence: ABSTRACT Joanna Czuwara MD, PhD Introduction. Dermatoscope is a tool for a skin examination, used especially in early detection of malignant skin Department of Dermatology lesions. Non-dermatologists are being trained for opportunistic melanoma detection with the usage of dermato- Medical University of Warsaw, Poland scopy, however, still non-satisfactory. This study was aimed to determine whether practical dermoscopy adjunct Koszykowa 82A, 02–008 Warszawa to traditional, lecture and seminar-based medical school curriculum would improve the perceived relevance of e-mail: [email protected] regular skin examination and basic skin lesions differentiation. Material and method. Fourth-year medical students participating in a 3-week-long dermatology course were randomly assigned to two groups: the first one called A with limited access to a dermatoscope and the second one called B, with unlimited access to dermatoscopes throughout the course. All participants answered surveys concerning their attitude towards skin examination, with a rating scale from 1 to 5, before and after the course. Also, all participants completed an image-based dermoscopy test for distinguishing benign from malignant skin lesions. Results. Students assigned to group B significantly improved their perceived importance of routine skin examination (mean scores before 4.38; after 4.57, P = 0.03). No such tendency was observed in group A — before 4.40, after 4.49 (P = 0.29). -
Misdiagnosed, Mistreated and Delay
erimenta xp l D E e r & m l a a t c o i l n o i Journal of Clinical & Experimental Scalvenzi et al., J Clin Exp Dermatol Res 2012, S:6 l g y C f R DOI: 10.4172/2155-9554.S6-002 o e l ISSN: 2155-9554 s a e n a r r u c o h J Dermatology Research Research Article Open Access Misdiagnosed, Mistreated and Delay Diagnosed Acral Melanoma: The Atypical Presentations Scalvenzi M*, Palmisano F and Costa C Departments of Dermatology, University of Naples Federico II, Italy Abstract Background: Acral skin is the most common site of malignant melanoma in non-Caucasian population. Diagnosis in this anatomic site is often delayed because this area is not routinely examined by patients or primary physicians. Objective: To perform an earlier diagnosis underlining the importance of dermoscopy helping clinicians to differentiate this disease from the other lesions and biopsies will result in more timely diagnoses and improved survival. Methods: We present 6 case studies visited in our Department of Dermatology of Naples University between October 2010 and September 2012. Results: These lesions often mimic other entities like warts, calli, bacterial or fungal infections, foreign bodies, vascular lesions, blisters, melanocytic nevi, subungual hematomas, pyogenic granulomas, onychomycosis, keratoacanthomas, diabetic foot ulcers, traumatic lesions that can lead to misdiagnosis and mistreatment. Conclusions: Awareness of atypical presentations of acral melanoma may be important to decrease misdiagnosis rates and improve patient outcome. Keywords: Acral melanoma; Foot; Misdiagnosis; Dermoscopy 5 cm in diameter (Figure 3a), misdiagnosed as a wart and treated for seven months with cryotherapy. -
Dermoscopy of Pigmented Skin Lesions (Part
Dermoscopy of Pigmented Skin Lesions* (Part II) H. Peter Soyer,a MD; Giuseppe Argenziano,b MD; Sergio Chimenti, c MD; Vincenzo Ruocco,b MD aDepartment of Dermatology, University of Graz, Graz, Austria bDepartment of Dermatology, Second University of Naples, Naples, Italy cDepartment of Dermatology, University Tor Vergata of Rome, Rome, Italy * This CME article is partly reprinted from the Book and CD-Rom ’Interactive Atlas of Dermoscopy’ with permission from EDRA (Medical Publishing & New Media) -- see also www.dermoscopy.org Corresponding author: H. Peter Soyer, MD Department of Dermatology, University of Graz Auenbruggerplatz 8 - A-8036 Graz, Austria Phone: 0043-316-385-3235 Fax: 0043-0316-385-4957 E-mail: [email protected] Key words: dermoscopy, dermatoscopy, epiluminescence microscopy, incident light microscopy, skin surface microscopy, melanoma, pigmented skin lesions, clinical diagnosis 1 Dermoscopy is a non-invasive technique combining digital photography and light microscopy for in vivo observation and diagnosis of pigmented skin lesions. For dermoscopic analysis, pigmented skin lesions are covered with liquid (mineral oil, alcohol, or water) and examined under magnification ranging from 6x to 100x, in some cases using a dermatoscope connected to a digital imaging system. The improved visualization of surface and subsurface structures obtained with this technique allows the recognition of morphologic structures within the lesions that would not be detected otherwise. These morphological structures can be classified on -
The ABCD Rule of Dermatoscopy
The ABeD rule of dermatoscopy High prospective value in the diagnosis ofdoubtful melanocytic skin lesions Franz Nachbar, MD,a Wilhelm Stolz, MD,b Tanja Merkle, MD,a Armand B. Cognetta, MD,c Thomas Vogt, MD,b Michael Landthaler, MD,b Peter Bilek," Otto Braun-Falco, MD,a and Gerd Plewig, MDa Munich and Regensburg, Germany, and Tallahassee, Florida Background: The difficulties in accuratelyassessing pigmented skinlesions are ever present in practice. The recentlydescribed ABCD rule of dermatoscopy(skin surface microscopy at XIO magnification), based on the criteria asymmetry (A), border (B), color (C), and differential structure (D), improved diagnostic accuracy when applied retrospectively to clinical slides. Objective: A study was designed to evaluatethe prospectivevalueof the ABCD rule of der matoscopy in melanocyticlesions. Methods: In 172melanocytic pigmented skin lesions, the criteria of the ABeD rule of der matoscopy were analyzed with a semiquantitativescoring system before excision. Results:Accordingto the retrospectively determined threshold, tumors with a score higher than 5.45 (64/69 melanomas[92.8%]) wereclassified as malignant,whereas lesionswith a lowerscorewereconsideredas benign(93/103 melanocyticnevi [90.3%n.Negative predic tivevaluefor melanoma (True-Negative+ [True-Negative+ False-Negative)) was 95.8%, whereas positive predictive value (True-Positive+ [True-Positive + False-Positivel) was 85.3%. Diagnostic accuracy for melanoma (True-Positive + [True-Positive+ False Positive + False-Negative])was80.0%,comparedwith64.4% by the nakedeye. Melanoma showed a mean final dermatoscopy SCore of 6.79 (SD, ± 0.92), significantly differing from melanocytic nevi (mean score,4.27 ± 0.99; p < O.oI , U test), Conclusion: The ABeD rule can be easilylearned and rapidly calculated, and has proven to be reliable. -
Dermoscopic Patterns of Acral Melanocytic Lesions in Skin of Color
SKIN OF COLOR IN COLLABORATION WITH THE SKIN OF COLOR SOCIETY Dermoscopic Patterns of Acral Melanocytic Lesions in Skin of Color Andrea Tan, BS; Jennifer A. Stein, MD, PhD Population Trends in Skin of Color PRACTICE POINTS Much of the literature on malignant melanoma his- • Dermatologists should be familiar with common torically has involved non-Hispanic white patients, but dermoscopic patterns seen at acral sites in patients the incidence in lighter-skinned populations has been with skin of color as well as the most up-to-date increasing steadily over the last few decades.1 Although diagnostic algorithms. ALM can occur in any race, it disproportionately affects • Acral lentiginous melanoma should be strongly sus- skin of color populations;copy ALM accounts for only 0.8% to pected if dermoscopy reveals a parallel ridge pattern 1% of all melanomas in white populations, but it consti- or if dermoscopy of volar skin reveals a lack of typi- tutes 4% to 58% of melanomas in ethnic populations and cal dermoscopic patterns in lesions with a diameter is the most common melanoma subtype among black greater than 7 mm. Americans.2-5 Acral lentiginous melanoma also is associ- atednot with a worse prognosis compared to other subtypes, which may indicate a more aggressive biological nature6 but also may point toward socioeconomic and cultural Acral lentiginous melanoma (ALM) is a rare but aggressive subtype barriers (eg, low income or education levels, lack of insur- of melanoma often associated with poor prognosis. Although overallDo incidence is rare, ALM accounts for a larger proportion of mela- ance, lower health literacy), leading to disparities in access 5 nomas among black, Asian, and Hispanic individuals than among to care and diagnosis at advanced stages. -
Pathology of Acral Nevi and Melanomas
Acral Melanoma D Elder, Maui, HI 2020 Subtlety and Uncertainty • More Common in Sun-Susceptible Populations: • Pathway I. Low CSD Melanoma/Superficial Spreading Melanoma (SSM) • Pathway II. High CSD Melanoma/Lentigo Maligna Melanoma (LMM) • Pathway III. Desmoplastic Melanoma • Incidence about the same world-wide • Pathway IV. Malignant Spitz Tumor (?) • Pathway V. Acral Melanoma • Pathway VI. Mucosal Melanoma • Pathway VII. Melanoma in Congenital Nevus (MCN) • Pathway VIII. Melanoma in Blue Nevus (MBN) • Pathway IX. Uveal Melanoma • Variable Pathways: Nodular Melanoma Lv, Jiaojie, et al (Shanghai, 2016) Table 1. Classification of Melanocytic Tumors by Epidemiologic, Clinical, Histopathologic & Genomic Attributes Role of UV: Low UV High UV Low to No (or Variable) CSD Pathway: I II III IV V VI VII VIII IX High-CSD Melanoma in Low-CSD Melanoma Desmoplastic Spitz Mucosal Melanoma Melanoma Acral Melanoma Congenital Uveal Melanoma Melanoma Melanoma Melanoma In Blue Nevus Superficial Spreading Melanoma (LMM) Nevus Congenital Nevus ? IAMP ? IAMP Spitz Nevus ?IAMP Melanosis Blue Nevus ? Benign Nevus (CN) Atypical Nodular Borderline Low Grade Atypical Spitz Atypical Cellular Blue ? IAMP ? IAMP melanocytic proliferation in Uveal nevus Dysplasia nevus melanosis Nevus Low Bap-1 Deficiency DPN PEM proliferation CN Melanocytoma Melanocytoma Melanocytoma /MELTUMP /MELTUMP /MELTUMP Borderline High Grade IAMPUS/ Lentigo maligna Melanoma in situ STUMP Melanoma in situ ? MIS in CN Atypical CBN ? High Dysplasia SAMPUS Superficial Mucosal Melanoma in Melanoma