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Dermoscopy, with and without visual inspection, for diagnosing melanoma in adults

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      Cancer incidence and mortality worldwide: sources, methods and major patterns in GLOBOCAN 2012.

      Estimates of the worldwide incidence and mortality from 27 major cancers and for all cancers combined for 2012 are now available in the GLOBOCAN series of the International Agency for Research on Cancer. We review the sources and methods used in compiling the national cancer incidence and mortality estimates, and briefly describe the key results by cancer site and in 20 large "areas" of the world. Overall, there were 14.1 million new cases and 8.2 million deaths in 2012. The most commonly diagnosed cancers were lung (1.82 million), breast (1.67 million), and colorectal (1.36 million); the most common causes of cancer death were lung cancer (1.6 million deaths), liver cancer (745,000 deaths), and stomach cancer (723,000 deaths). © 2014 UICC.
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        QUADAS-2: a revised tool for the quality assessment of diagnostic accuracy studies.

        In 2003, the QUADAS tool for systematic reviews of diagnostic accuracy studies was developed. Experience, anecdotal reports, and feedback suggested areas for improvement; therefore, QUADAS-2 was developed. This tool comprises 4 domains: patient selection, index test, reference standard, and flow and timing. Each domain is assessed in terms of risk of bias, and the first 3 domains are also assessed in terms of concerns regarding applicability. Signalling questions are included to help judge risk of bias. The QUADAS-2 tool is applied in 4 phases: summarize the review question, tailor the tool and produce review-specific guidance, construct a flow diagram for the primary study, and judge bias and applicability. This tool will allow for more transparent rating of bias and applicability of primary diagnostic accuracy studies.
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          Final version of 2009 AJCC melanoma staging and classification.

          To revise the staging system for cutaneous melanoma on the basis of data from an expanded American Joint Committee on Cancer (AJCC) Melanoma Staging Database. The melanoma staging recommendations were made on the basis of a multivariate analysis of 30,946 patients with stages I, II, and III melanoma and 7,972 patients with stage IV melanoma to revise and clarify TNM classifications and stage grouping criteria. Findings and new definitions include the following: (1) in patients with localized melanoma, tumor thickness, mitotic rate (histologically defined as mitoses/mm(2)), and ulceration were the most dominant prognostic factors. (2) Mitotic rate replaces level of invasion as a primary criterion for defining T1b melanomas. (3) Among the 3,307 patients with regional metastases, components that defined the N category were the number of metastatic nodes, tumor burden, and ulceration of the primary melanoma. (4) For staging purposes, all patients with microscopic nodal metastases, regardless of extent of tumor burden, are classified as stage III. Micrometastases detected by immunohistochemistry are specifically included. (5) On the basis of a multivariate analysis of patients with distant metastases, the two dominant components in defining the M category continue to be the site of distant metastases (nonvisceral v lung v all other visceral metastatic sites) and an elevated serum lactate dehydrogenase level. Using an evidence-based approach, revisions to the AJCC melanoma staging system have been made that reflect our improved understanding of this disease. These revisions will be formally incorporated into the seventh edition (2009) of the AJCC Cancer Staging Manual and implemented by early 2010.
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            Author and article information

            Affiliations
            [1 ]University of Birmingham; Institute of Applied Health Research; Birmingham UK B15 2TT
            [2 ]University Hospitals Birmingham NHS Foundation Trust and University of Birmingham; NIHR Birmingham Biomedical Research Centre; Birmingham UK
            [3 ]Churchill Hospital; Department of Dermatology; Old Road Headington Oxford UK OX3 7LE
            [4 ]St George's Hospital; Department of Plastic Surgery; London UK
            [5 ]Oxford University Hospitals NHS Foundation Trust; Department of Plastic and Reconstructive Surgery; Oxford UK
            [6 ]NHS Lothian/University of Edinburgh; Department of Plastic Surgery; 25/6 India Street Edinburgh UK EH3 6HE
            [7 ]University Hospital of Wales; Welsh Institute of Dermatology; Heath Park Cardiff UK CF14 4XW
            [8 ]Norfolk and Norwich University Hospital NHS Trust; Department of Plastic and Reconstructive Surgery; Colney Lane Norwich UK NR4 7UY
            [9 ]School of Medicine; Division of Epidemiology and Public Health; University of Nottingham Nottingham UK NG7 2UH
            [10 ]The University of Nottingham; c/o Cochrane Skin Group; Nottingham UK
            [11 ]University of Cambridge; Public Health & Primary Care; Strangeways Research Laboratory, Worts Causeway Cambridge UK CB1 8RN
            [12 ]University of Nottingham; Centre of Evidence Based Dermatology; Queen's Medical Centre Derby Road Nottingham UK NG7 2UH
            Journal
            Cochrane Database of Systematic Reviews
            Wiley
            14651858
            December 04 2018
            10.1002/14651858.CD011902.pub2
            (Editor)
            © 2018
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