Identifying Skin Cancer
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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 -
Short Course 11 Pigmented Lesions of the Skin
Rev Esp Patol 1999; Vol. 32, N~ 3: 447-453 © Prous Science, SA. © Sociedad Espafiola de Anatomfa Patol6gica Short Course 11 © Sociedad Espafiola de Citologia Pigmented lesions of the skin Chairperson F Contreras Spain Ca-chairpersons S McNutt USA and P McKee, USA. Problematic melanocytic nevi melanin pigment is often evident. Frequently, however, the lesion is solely intradermal when it may be confused with a fibrohistiocytic RH. McKee and F.R.C. Path tumor, particularly epithelloid cell fibrous histiocytoma (4). It is typi- cally composed of epitheliold nevus cells with abundant eosinophilic Brigham and Women’s Hospital, Harvard Medical School, Boston, cytoplasm and large, round, to oval vesicular nuclei containing pro- USA. minent eosinophilic nucleoli. Intranuclear cytoplasmic pseudoinclu- sions are common and mitotic figures are occasionally present. The nevus cells which are embedded in a dense, sclerotic connective tis- Whether the diagnosis of any particular nevus is problematic or not sue stroma, usually show maturation with depth. Less frequently the nevus is composed solely of spindle cells which may result in confu- depends upon a variety of factors, including the experience and enthusiasm of the pathologist, the nature of the specimen (shave vs. sion with atrophic fibrous histiocytoma. Desmoplastic nevus can be distinguished from epithelloid fibrous histiocytoma by its paucicellu- punch vs. excisional), the quality of the sections (and their staining), larity, absence of even a focal storiform growth pattern and SiQO pro- the hour of the day or day of the week in addition to the problems relating to the ever-increasing range of histological variants that we tein/HMB 45 expression. -
On the Histological Diagnosis and Prognosis of Malignant Melanoma
J Clin Pathol: first published as 10.1136/jcp.33.2.101 on 1 February 1980. Downloaded from J Clin Pathol 1980, 33: 101-124 On the histological diagnosis and prognosis of malignant melanoma ARNOLD LEVENE Hunterian Professor, Royal College of Surgeons, and Department of Histopathology, The Royal Marsden Hospital, Fulham Road, London SW3, UK SUMMARY This review deals with difficulties of diagnosis in cutaneous malignant melanoma encountered by histopathologists of variable seniority and is based on referred material at The Royal Marsden Hospital over a 20-year period and on the experience of more than two-and-a-half thousand cases referred to The World Health Organisation Melanoma Unit which I reviewed when chairman of the Pathologists' Committee. Though there is reference to the differential diagnosis of primary and metastatic tumour, the main concern is with establishing the diagnosis of primary melanoma to the exclusion of all other lesions. An appendix on recommended diagnostic methods in cutaneous melanomas is included. Among the difficult diagnostic fields in histopathol- not to be labelled malignant because it 'looks nasty'. ogy melanocytic tumours have achieved a notoriety. Thus, until the critical evaluation of the 'malignant Accurate diagnosis, however, is of major clinical melanoma of childhood' by Spitz (1948) the naevus importance for the following reasons: with which this investigator's name is associated was 1 The management of the primary lesion is reckoned among the malignancies on histological principally by surgical excision with a large margin grounds. of normal appearing skin. The consequences of over-diagnosis are those of major disfiguring surgery Naevus and melanoma cells http://jcp.bmj.com/ and its morbidity. -
Lumps & Bumps: Approach to Common Dermatologic Neoplasms
Case-Based Approach to Common Dermatologic Neoplasms Patrick Retterbush, MD, FAAD Mohs Surgery & Dermatologic Oncology Associate Member of the American College of Mohs Surgery Private Practice: Lockman Dermatology January 27th 2018 Disclosure of Relevant Financial Relationships • I do not have any relevant financial relationships, commercial interests, and/or conflicts of interest regarding the content of this presentation. Goals/Objectives • Recognize common benign growths • Recognize common malignant growths • Useful clues & examination for evaluating melanocytic nevi and when to be concerned for melanoma/atypical moles • How to perform a basic skin biopsy and which method/type to choose • Basic treatment/when to refer Key Questions & Physical Examination Findings for a Growth History Physical Examination • How long has the lesion been • Describing a growth present? – flat or raised? • flat – macule (<1cm) or patch (>1cm) – years, months, weeks • raised – papule (<1cm) or plaque (>1cm) – nodule if deep (majority of lesion in • Has it changed? dermis/SQ) – Size – secondary descriptive features • scaly (hyperkeratosis, retention of strateum – Shape corneum) – Color • crusty (dried serum, blood, or pus on surface) • eroded or ulcerated (partial vs. full thickness – Symptoms – pain, bleeding, itch? epidermal loss) – Over what time frame? • color (skin colored, red, pigmented, pearly) • feel (hard or soft, mobile or fixed) • PMH: • size: i.e. 6 x 4mm – prior skin cancers • Look at the rest of the skin/region of skin • SCC/BCCs vs. melanoma -
The State of the Dysplastic Nevus in the 21St Century
The State of the Dysplastic Nevus in the 21st Century Keith Duffy, MD Associate professor Department of Dermatology University of Utah Department of Dermatology Disclosures • Myriad Genetics – Advisory board; honorarium • Castle Biosciences – Advisory board; honorarium What do I do? • Clinical – 60% Mohs micrographic and reconstructive surgery and high risk skin cancer – 40% Dermatopathology sign-out – Multidisciplinary cutaneous oncology program – Huntsman Cancer Institute • Administrative – Residency Program Director, Dermatology Department of Dermatology Department of Dermatology The current(ish) state of affairs… Do you believe dysplastic (Clark) nevi are truly premalignant lesions? 53% A. Yes B. No 25% C. Unsure 22% A. B. C. How do you report “dysplastic nevi”? A. Dysplastic nevus 62% B. Clark nevus C. Nevus with architectural disorder 19% D. Other 12% 7% A. B. C. D. Do you assign a histologic “grade” to these nevi? 87% A. Yes B. No 13% A. B. If yes, what grading system do you use? A. Cytology as three grades (mild, moderate, 73% severe) B. Cytology and architecture as two separate grades C. Cytology as two grades 8% 10% 10% only D. Other grading system A. B. C. D. Brief history • 1978 – Dr. Clark describes nevi associated with melanoma prone families – The B-K mole syndrome • 1978 – Dr. Lynch describes a single multi- generational family with melanoma and nevi – Familial atypical multiple mole melanoma syndrome (FAMMM) Brief history • 1980 – Dr. Elder and Clark describe ‘dysplastic nevi’ in a non-familial setting – Introduction of the term ‘dysplastic nevus syndrome’ • Familial and sporadic variants • Formally postulated that ‘dysplastic nevi’ are precursors of melanoma Dr. -
Lentigo Maligna Melanoma and Simulants Maui January 2020 Superficial Atypical Melanocytic Proliferations
Superficial Atypical Melanocytic Proliferations II. Lentigo Maligna Melanoma and Simulants Maui January 2020 Superficial Atypical Melanocytic Proliferations • RGP Melanomas • SSM, LMM, ALM, MLM • Intermediate lesions • Dysplastic nevi, Atypical lentiginous proliferations in high CSD skin; Atypical Acral lentiginous nevi • Superficial atypical melanocytic proliferations • Pagetoid plaque-like Spitz nevi; pigmented spindle cell nevus (Reed) • Special site nevi (genital, breast, scalp, ear, flexural, etc). • Superficial atypical melanocytic proliferations of uncertain significance • Atypical/unusual/uncertain examples of all of the above Superficial Atypical Melanocytic Proliferations • RGP Melanomas • SSM, LMM, ALM, MLM • Intermediate lesions • Dysplastic nevi, Atypical lentiginous proliferations in high CSD skin; Atypical Acral lentiginous nevi • Superficial atypical melanocytic proliferations • Pagetoid plaque-like Spitz nevi; pigmented spindle cell nevus (Reed) • Special site nevi (genital, breast, scalp, ear, flexural, etc). • Superficial atypical melanocytic proliferations of uncertain significance • Atypical/unusual/uncertain examples of all of the above High CSD Melanomas and Simulants. D Elder, Maui, HI Jan 2020 Lentigo maligna melanoma Atypical lentiginous nevi/proliferations High CSD: Lentiginous Nevi and Lentigo Maligna Melanoma and Simulant(s) • Lentiginous Melanoma of Sun-Damaged Skin • LMM in situ • LMM invasive • Distinction from Dysplastic Nevi (Dysplastic Nevus-like Melanoma/Nevoid Lentigo Maligna • Lentiginous Nevi of -
Dysplastic Nevus Panel Discussion
Dysplastic Nevus Panel Discussion Maxwell Fung, MD, Moderator Director, UC Davis Dermatopathology Service Kerri Rieger, MD PhD Stanford Dermatopathology Service Joshua Schulman, MD Director of Dermatopathology, Sacramento Veterans Affairs Medical Center Definitions, Diagnostic criteria Dysplastic nevus • Major criteria (required) • basilar proliferation of atypical melanocytes extending 3 rete ridges beyond a dermal component (if present) i.e. “shoulder” • intraepidermal melanocytic proliferation (lentiginous or epithelioid) • Minor criteria (≥ 2) • fusion of rete ridges • concentric/lamellar eosinophilic fibrosis • inflammatory host response • neovascularization Clemente C, et al. Histopathologic diagnosis of dysplastic nevi: concordance among pathologists convened by the WHO Melanoma Programme. Hum Pathol 1991;22:313-19. Naeyaert JM, Brochez L. Dysplastic nevi. N Eng J Med 2003;23:349:2233-2240 Atypical nevus/mole Fig 1. Duffy K, Grossman D. • Usually 4-12 mm The dysplastic nevus. J Am Acad Dermatol 2012;67:19:31-12. • Asymmetry • Irregular pigmentation • Irregular border pigmented • Ill-defined border seborrheic keratosis • Macular component, usually peripheral Dysplastic nevus syndrome atypical mole syndrome, B-K mole syndrome, familial melanoma syndrome, familial atypical multiple mole-melanoma (FAMMM) • OMIM #155600 NIH Consensus criteria Occurrence of melanoma in ≥1 first- or second-degree relatives Large number of nevi (often >50), some of which are clinically atypical (and) Nevi with certain distinct histologic features Dutch -
Second Revised Proposed Regulation of the State
SECOND REVISED PROPOSED REGULATION OF THE STATE BOARD OF HEALTH LCB File No. R057-16 February 5, 2018 EXPLANATION – Matter in italics is new; matter in brackets [omitted material] is material to be omitted. AUTHORITY: §§1, 2, 4-9 and 11-15, NRS 457.065 and 457.240; §3, NRS 457.065 and 457.250; §10, NRS 457.065; §16, NRS 439.150, 457.065, 457.250 and 457.260. A REGULATION relating to cancer; revising provisions relating to certain publications adopted by reference by the State Board of Health; revising provisions governing the system for reporting information on cancer and other neoplasms established and maintained by the Chief Medical Officer; establishing the amount and the procedure for the imposition of certain administrative penalties by the Division of Public and Behavioral Health of the Department of Health and Human Services; and providing other matters properly relating thereto. Legislative Counsel’s Digest: Existing law defines the term “cancer” to mean “all malignant neoplasms, regardless of the tissue of origin, including malignant lymphoma and leukemia” and, before the 78th Legislative Session, required the reporting of incidences of cancer. (NRS 457.020, 457.230) Pursuant to Assembly Bill No. 42 of the 78th Legislative Session, the State Board of Health is: (1) authorized to require the reporting of incidences of neoplasms other than cancer, in addition to incidences of cancer, to the system for reporting such information established and maintained by the Chief Medical Officer; and (2) required to establish an administrative penalty to impose against any person who violates certain provisions which govern the abstracting of records of a health care facility relating to the neoplasms the Board requires to be reported. -
Dysplastic Nevi” Derm Surg 2015: 41:1 (159-161)
Reagan Anderson, FAOCD, FAAD, FASMS, CAQ Mohs, MPH, MCS Founder of Your Health University Given published data on the very low likelihood that incompletely biopsied DN will recur as melanoma, it does not seem reasonable to suggest that all DN require re- excision. Given the fact that some DN turn out to be invasive melanoma when re-excised (such as in the article in question), some DN should clearly be re-excised. As dermatologists, we all struggle with the decision regarding observation versus re- excision, particularly when the atypia has been characterized as “severe.” Bowen, Glen. Commentary on Melanoma Diagnosed Following Excision of “Dysplastic Nevi” Derm Surg 2015: 41:1 (159-161). Dysplastic Nevi (DN) were first reported in 1978 by Clark and colleagues. ◦ These were histologic categorizations of nevi found in patients who were “melanoma prone” due to family history. ◦ Later they were known as dysplastic nevi as they had architectural and cytologic atypia (similar concept to cervical dysplasia) Dysplastic is more of a histologic term. Some don’t use it as there is no consensus on how to grade. Atypia is more of a clinical term. However, no term has universal acceptance. Estimated they occur in about 10% of the population of Northern European dissent (7-21%) Pts with a history of melanoma – 34-59% have DN Tucker MA, Goldstein AM. Melanoma etiology: where are we? Oncogene 2003;22:3042–52. 22. Tucker MA. Melanoma epidemiology. Hematol Oncol Clin North Am 2009;23:383– 95. Melanomas are usually are found in sun- exposed areas (chronic or intermittent). Usually in later years of life although due to tanning beds this is changing. -
Skin Tumors Process, Starting at Young Age (20 Years), with the Based on Its Differentiation Into Keratinocytic, Tumors Developing 30 to 40 Years Later (Fig 22-2)
Pathology of Cancer El Bolkainy et al 5th edition, 2016 The skin consists of epidermis, dermis and the Cutaneous malignancies account for nearly half subcutaneous fat. The epidermis contains different of all cancers in the Unites States. In Australia and types of cells each representing a specific lineage. New Zealand, where the incidence of skin cancer These include keratinocytes, melanocytes, is the highest in the world, the total number of Langerhans and Merkel cells (Elder et al, 2005). skin cancer exceeds that of all other cancers The epidermis is divided into 4 layers; stratum combined by several folds (Ch'ng et al, 2006). Non basale (basal cell layer), stratum spinosum (spinous melanoma skin cancer is not registered in USA cell layer), stratum granulosum (granular cell layer), and UK national registries because it is almost and stratum corneum (Fig 22-1). The dermis has 2 curable by simple surgical excision. The variations layers; a superficial (papillary dermis) and deep of incidence in distinct geographic areas are (reticular dermis) layers. The dermis contains probably related to the degree of skin supporting stroma, blood vessels and hemato- pigmentation of the population. The median age at lymphoid cells. The basal layer of the epidermis is diagnosis of skin cancer (excluding basal and attached to the superficial dermis by the basement squamous cell carcinoma) was 61 years (Howlader membrane. There are five appendages in normal et al, 2011). In Egypt, skin cancer constituted 4% skin; hair, nail, apocrine, eccrine, and sebaceous of total malignancies, affects mainly adults with glands. The hair follicle, sebaceous glands and male predominance (1.5:1) (Mokhtar et al, 2007). -
Managing Melanoma in Situ Kristen L
Managing Melanoma In Situ Kristen L. Toren, MD, and Eric C. Parlette, MD† Melanoma is a highly aggressive skin cancer with an increasing incidence. Melanoma in situ is an early, non-invasive form in which the tumor is confined to the epidermis. Treatment of melanoma in situ is challenging due to the frequent subclinical microscopic spread and to the presentation on the head and neck in cosmetically sensitive areas with chronic sun damage. Optimizing tumor eradication is imperative to reduce the potential progression into invasive disease and metastasis, all while maintaining cosmesis. Multiple treatment regimens have been implemented for managing difficult melanoma in situ tu- mors. We provide a thorough review of surgical, and non-surgical, management of mela- noma in situ which can pose therapeutic dilemmas due to size, anatomic location, and subclinical spread. Semin Cutan Med Surg 29:258-263 © 2010 Elsevier Inc. All rights reserved. elanoma is a highly aggressive form of skin cancer with ciated with a greater risk of melanoma, with the exception of Man increasing incidence.1 Melanoma in situ (MIS) is an lentigo maligna. Lentigo maligna, unlike other melanomas, early form of melanoma in which the malignancy is confined has a greater association with nonmelanoma skin cancers.3 to the epidermis. According to the American Cancer Society, an estimated 68,720 new cases of malignant melanoma were Diagnostic Criteria reported in 2009, and 53,120 new cases of melanoma in situ. Lentigo maligna is a subtype of MIS found on sun-exposed Melanoma in situ can have a highly variable presentation, areas and accounts for approximately 80% of all MIS tu- from a well-demarcated, small brown macule on healthy- mors.2 With its increasing incidence and being a precursor to appearing skin to an asymmetric, variably pigmented large invasive melanoma, the treatment of MIS, in particular len- patch on grossly actinically damaged skin (Fig. -
Guidelines for the Management of Cutaneous Melanoma 2010 J.R
BJD BAD GUIDELINES British Journal of Dermatology Revised U.K. guidelines for the management of cutaneous melanoma 2010 J.R. Marsden, J.A. Newton-Bishop,* L. Burrows, M. Cook,à P.G. Corrie,§ N.H. Cox,– M.E. Gore,** P. Lorigan, R. MacKie,àà P. Nathan,§§ H. Peach,–– B. Powell*** and C. Walker University Hospital Birmingham, Birmingham B29 6JD, U.K. *University of Leeds, Leeds LS9 7TF, U.K. Salisbury District Hospital, Salisbury SP2 8BJ, U.K. àRoyal Surrey County Hospital NHS Trust, Guildford GU2 7XX, U.K. §Cambridge University Hospitals NHS Foundation Trust, Cambridge CB2 2QQ, U.K. –Cumberland Infirmary, Carlisle CA2 7HY, U.K. **Royal Marsden Hospital, London SW3 6JJ, U.K. The Christie NHS Foundation Trust, Manchester M20 4BX, U.K. ààUniversity of Glasgow, Glasgow G12 8QQ, U.K. §§Mount Vernon Hospital, London HA6 2RN, U.K. ––St James’s University Hospital, Leeds LS9 7TF, U.K. ***St George’s Hospital, London SW17 0QT, U.K. Correspondence Disclaimer Jerry Marsden. These guidelines reflect the best published data available at the time the report was E-mail: [email protected] prepared. Caution should be exercised in interpreting the data; the results of future Accepted for publication studies may require alteration of the conclusions or recommendations in this report. 24 May 2010 It may be necessary or even desirable to depart from the guidelines in the interests of Key words specific patients and special circumstances. Just as adherence to the guidelines may not evidence, guideline, investigation, melanoma, treatment constitute defence against a claim of negligence, so deviation from them should not necessarily be deemed negligent.