Misdiagnosed, Mistreated and Delay
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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. -
Nonpigmented Metastatic Melanoma in a Two-Year-Old Girl: a Serious Diagnostic Dilemma
Hindawi Publishing Corporation Case Reports in Oncological Medicine Volume 2015, Article ID 298273, 3 pages http://dx.doi.org/10.1155/2015/298273 Case Report Nonpigmented Metastatic Melanoma in a Two-Year-Old Girl: A Serious Diagnostic Dilemma Gulden Diniz,1 Hulya Tosun Yildirim,2 Selcen Yamaci,2 and Nur Olgun3 1 Izmir Tepecik Education and Research Hospital, Pathology Laboratory, Turkey 2Izmir Dr. Behcet Uz Children’s Hospital, Pathology Laboratory and Dermatology Clinics, Turkey 3Pediatric Oncology Clinics, Izmir Dokuz Eylul University, Turkey Correspondence should be addressed to Gulden Diniz; [email protected] Received 23 July 2014; Revised 20 January 2015; Accepted 21 January 2015 Academic Editor: Francesca Micci Copyright © 2015 Gulden Diniz et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. Although rare, malignant melanoma may occur in children. Childhood melanomas account for only 0.3–3% of all melanomas. In particular the presence of congenital melanocytic nevi is associated with an increased risk of development of melanoma. We herein report a case of malignant melanoma that developed on a giant congenital melanocytic nevus and made a metastasis to the subcutaneous tissue of neck in a two-year-old girl. The patient was hospitalized for differential diagnosis and treatment of cervical mass with a suspicion of hematological malignancy, because the malignant transformation of congenital nevus was not noticed before. In this case, we found out a nonpigmented malignant tumor of pleomorphic cells after the microscopic examination of subcutaneous lesion. -
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. -
Amelanotic Melanoma: a Unique Case Study and Review of the Literature Katherine a Kaizer-Salk,1 Robert J Herten,2 Bruce D Ragsdale,3 Roberta D Sengelmann1,4
Reminder of important clinical lesson CASE REPORT Amelanotic melanoma: a unique case study and review of the literature Katherine A Kaizer-Salk,1 Robert J Herten,2 Bruce D Ragsdale,3 Roberta D Sengelmann1,4 1Santa Barbara Skin Institute, SUMMARY melanoma in situ, lentigo maligna type (MISLMA). Santa Barbara, California, USA Amelanotic melanoma (AM) is a rare form of melanoma At this point, the patient was referred for treatment. 2 Dermatology and which lacks visible pigment. Due to the achromic On clinical exam, the lesion appeared as Dermatopathology, University manifestation of this atypical cutaneous malignancy, accuminate, pink and flesh-coloured papules with of California Irvine School of it has been difficult to establish clinical criteria for no pigment on dermatoscopy (figure 2). The Medicine, Irvine, California, USA 3Department of diagnosis. Thus, AM often progresses into an invasive pronounced telangiectasia in the malar region is Dermatopathology, Western disease due to delayed diagnosis. In this report, we consistent with the patient’s history of erythema- Diagnostic Services Laboratory, describe the case of a 72-year-old Caucasian woman tous rosacea, as this vascular prominence predated Santa Maria, California, USA who had been diagnosed with AM after 3 years of her use of topical corticosteroids. Only on Wood’s 4Department of Dermatology, failed treatments for what presented as a periorbital lamp exam was there some evidence of melanin University of California Irvine dermatitis. Her Clark’s level 4, 1.30 mm thick melanoma along the left lower eyelid. Below the left eyelid School of Medicine, Irvine, required nine surgeries for successful resection and was a crescentic area of hypopigmented skin that California, USA reconstruction. -
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. -
Things That Go Bump in the Light. the Differential Diagnosis of Posterior
Eye (2002) 16, 325–346 2002 Nature Publishing Group All rights reserved 0950-222X/02 $25.00 www.nature.com/eye IG Rennie Things that go bump THE DUKE ELDER LECTURE 2001 in the light. The differential diagnosis of posterior uveal melanomas Eye (2002) 16, 325–346. doi:10.1038/ The list of lesions that may simulate a sj.eye.6700117 malignant melanoma is extensive; Shields et al4 in a study of 400 patients referred to their service with a pseudomelanoma found these to encompass 40 different conditions at final diagnosis. Naturally, some lesions are Introduction mistaken for melanomas more frequently than The role of the ocular oncologist is two-fold: others. In this study over one quarter of the he must establish the correct diagnosis and patients referred with a diagnosis of a then institute the appropriate therapy, if presumed melanoma were subsequently found required. Prior to the establishment of ocular to have a suspicious naevus. We have recently oncology as a speciality in its own right, the examined the records of patients referred to majority of patients with a uveal melanoma the ocular oncology service in Sheffield with were treated by enucleation. It was recognised the diagnosis of a malignant melanoma. that inaccuracies in diagnosis occurred, but Patients with iris lesions or where the the frequency of these errors was not fully diagnosis of a melanoma was not mentioned appreciated until 1964 when Ferry studied a in the referral letter were excluded. During series of 7877 enucleation specimens. He the period 1985–1999 1154 patients were found that out of 529 eyes clinically diagnosed referred with a presumed melanoma and of as containing a melanoma, 100 harboured a these the diagnosis was confirmed in 936 lesion other than a malignant melanoma.1 cases (81%). -
Amelanotic Melanoma Jürgen Kreusch IV.3
Chapter IV.3 Amelanotic Melanoma Jürgen Kreusch IV.3 Contents IV.3.1 Introduction and Definition. 204 IV.3.2 Hypomelanotic and Amelanotic Melanoma. 204 IV.3 IV.3.4 Clinical Features. 205 IV.3.5 Dermoscopic Criteria. 207 IV.3.6 Adequate Dermoscopic Inspection of Non-pigmented Lesions . 208 IV.3.7 Dermoscopic Features of Amelanotic Melanoma . 208 IV.3.8 Vascular Patterns Fig. IV.3.1. Amelanotic melanoma (center; SSM, L III, in Amelanotic Melanoma. 208 0.6 mm) IV.3.9 Morphological Changes of Vessels During Tumor Growth. 209 summarized under this general term; however, IV.3.10 Relevant Clinical Differential amelanotic melanoma will not be identified by Diagnosis. 210 dermoscopy nor by any other diagnostic meth- IV.3.10.1 The Way to Diagnosis od if a lesion is not considered worth inspection of Amelanotic Melanoma . 210 with the particular instrument – a screening IV.3.10.2 Strategies for Detecting Amelanotic strategy including knowledge of clinical fea- Melanoma. 211 tures, dermoscopic techniques and criteria is References. 212 essential to spot amelanotic melanoma among the variety of non-pigmented lesions of the skin (Figs. IV.3.1, IV.3.5a). IV.3.1 Introduction and Definition IV.3.2 Hypomelanotic and Amelanotic Melanoma “Amelanotic melanoma” is a clinical and de- scriptive term frequently used for any melano- Frequently, melanoma are classified “amelanot- ma lacking melanin pigmentation. These tu- ic” regardless of the degree and nature of hy- mors represent a large fraction of the so-called popigmentation. One must distinguish two rea- “featureless” or “undiagnosable” melanoma [3– sons for a melanoma to contain little melanin. -
Enlargement of Choroidal Osteoma in a Child
OCULAR ONCOLOGY ENLARGEMENT OF CHOROIDAL OSTEOMA IN A CHILD A discussion and case report of the diagnosis and management of this rare tumor. BY MARIA PEFKIANAKI, MD, MSC, PHD; KAREEM SIOUFI, MD; AND CAROL L. SHIELDS, MD Choroidal osteoma On ultrasonography, the lesion demonstrated a hyper- is a rare intraocular echoic signal with posterior shadowing suggestive of calcifi- bony tumor that cation. On spectral domain enhanced depth imaging optical typically manifests coherence tomography (EDI-OCT), the mass extended under as a yellow-white, the foveola and there was no evidence of choroidal neovas- well-demarcated cular membrane (CNVM) or subretinal fluid (Figure 2). mass with geographic These features were suggestive of choroidal osteoma with pseudopodal mar- documentation of slow, slight enlargement. Given the pre- gins.1-3 This benign tumor predominantly occurs in the served visual acuity and subfoveal location of the osteoma, we peripapillary or papillomacular region, most often in young elected to observe the lesion. Calcium supplementation was women.1,2 Occasionally, choroidal osteoma can simulate an suggested to maintain calcification of the mass, as decalcifica- amelanotic choroidal tumor such as melanoma, nevus, or tion is a known factor predictive of poor visual outcome.6 metastasis.1,2 This tumor can also simulate choroidal inflam- matory disease such as sarcoidosis, tuberculosis, and other DISCUSSION causes of solitary idiopathic choroiditis.2,4 Due to its calcified Choroidal osteoma is a benign calcified tumor that can nature, -
Benign Versus Cancerous Lesions How to Tell the Difference – FMF 2014 Christie Freeman MD, CCFP, Dippderm, Msc
1 Benign versus Cancerous Lesions How to tell the difference – FMF 2014 Christie Freeman MD, CCFP, DipPDerm, MSc Benign lesions Seborrheic Keratoses: . Warty, stuck-on . Genetics and birthdays . Can start in late 20s…never stop . Many different presentations but all benign (ABCDEs don’t apply) . Treatment not covered. Dermoscopy: comedo-like openings, milia-like cysts, fissures, reg. hairpin vessels, fat fingers Dermatofibroma: . Benign fibrous skin lesion . Firm, pink or brown . Dimple to palpation . Often arises at site of minor injury that has been manipulated/ shaved over . Dermoscopy: central depigmented scar with surrounding peripheral network Intraepidermal nevus: Dome shaped nevi, often on the face Patients may have several of these 2 Can be confused with BCC, but firm, not friable, and under dermatoscope more comma-like/peripheral vessels (not arborizing) Sebaceous Hyperplasia: benign enlargement of the sebaceous lobule around a follicular opening present as one or multiple yellowish to skin coloured papules, often with a central dell they are seen most often on the nose, cheeks and forehead in middle aged to older individuals Under dermoscopy yellowish/white lobules around a central hair follicle with peripheral vessels Actinic Keratoses: . Skin coloured, pink or brown . Rough, sandpaper like crust (don’t just look, feel) . Sun exposed sites, fair-skinned older patients . Clinical variants . atrophic . pigmented . hyperkeratotic . cutaneous horn . confluent . actinic cheilitis . the initial lesion in the disease continuum that progresses to SCC . controversy as to whether these should be regarded as SCC in situ . 60% of SCC arise within an AK and 97% of SCCs have a contiguous AK 3 . range for risk of transformation in the literature is <1 % to 20% per year and lifetime risk for SCC in patients with multiple Aks is substantially increased . -
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 -
Amelanotic Melanoma
This is a repository copy of Easily missed? Amelanotic melanoma. White Rose Research Online URL for this paper: http://eprints.whiterose.ac.uk/127789/ Version: Accepted Version Article: Muinonen-Martin, AJ, O'Shea, SJ and Newton-Bishop, J orcid.org/0000-0001-9147-6802 (2018) Easily missed? Amelanotic melanoma. BMJ: British Medical Journal, 360 (8145). k826. ISSN 0959-8138 https://doi.org/10.1136/bmj.k826 © 2018, British Medical Journal Publishing Group. This manuscript version is made available under the CC BY-NC 4.0 license https://creativecommons.org/licenses/by-nc/4.0/ Reuse This article is distributed under the terms of the Creative Commons Attribution-NonCommercial (CC BY-NC) licence. This licence allows you to remix, tweak, and build upon this work non-commercially, and any new works must also acknowledge the authors and be non-commercial. You don’t have to license any derivative works on the same terms. More information and the full terms of the licence here: https://creativecommons.org/licenses/ Takedown If you consider content in White Rose Research Online to be in breach of UK law, please notify us by emailing [email protected] including the URL of the record and the reason for the withdrawal request. [email protected] https://eprints.whiterose.ac.uk/ Easily Missed: Amelanotic Melanoma Andy J Muinonen-Martin(1,2), Sally Jane O“(2), Julia Newton-Bishop(2) 1 York & Leeds Hospitals 2 Leeds Institute of Cancer and Pathology, University of Leeds Word count: 1181 A 50-year-old woman developed a bleeding nodule on the tip of the right index finger.