Evaluation of dynamic dermoscopic features of melanoma and benign naevi by sequential digital dermoscopic imaging and total body photography in a high‐risk Australian cohort

Background/Objectives Sequential digital dermoscopic imaging (SDDI) and total body photography (TBP) are recommended as a two‐step surveillance method for individuals at high‐risk of developing cutaneous melanoma. Dermoscopic features specific to melanoma have been well described, however, dynamic c...

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Veröffentlicht in:Australasian journal of dermatology 2023-02, Vol.64 (1), p.67-79
Hauptverfasser: Nguyen, Jennifer, Doolan, Brent J, Pan, Yan, Vestergaard, Tine, Paul, Eldho, McLean, Catriona, Haskett, Martin, Kelly, John, Mar, Victoria, Chamberlain, Alexander
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container_end_page 79
container_issue 1
container_start_page 67
container_title Australasian journal of dermatology
container_volume 64
creator Nguyen, Jennifer
Doolan, Brent J
Pan, Yan
Vestergaard, Tine
Paul, Eldho
McLean, Catriona
Haskett, Martin
Kelly, John
Mar, Victoria
Chamberlain, Alexander
description Background/Objectives Sequential digital dermoscopic imaging (SDDI) and total body photography (TBP) are recommended as a two‐step surveillance method for individuals at high‐risk of developing cutaneous melanoma. Dermoscopic features specific to melanoma have been well described, however, dynamic changes on serial imaging are less understood. This study aims to identify and compare dermoscopic features in developing melanomas and benign naevi that underwent SDDI and TBP to understand which dermoscopic features may be associated with a malignant change. Method Histopathology reports from a private specialist dermatology clinic from January 2007 to December 2019 were reviewed. Histopathologically confirmed melanoma and benign naevi that underwent SDDI and TBP with a minimum follow‐up interval of 3 months were included. Results Eighty‐nine melanomas (38.2% invasive, median Breslow thickness 0.35 mm, range: 0.2–1.45 mm) and 48 benign naevi were evaluated by three experienced dermatologists for dermoscopic changes. Features most strongly associated with melanoma included the development of neovascularisation, asymmetry and growth in pigment network, additional colours, shiny white structures, regression, structureless areas and change to a multi‐component pattern. The presence of atypical vessels (p = 0.02) and shiny white structures (p = 0.02) were significantly associated with invasive melanoma. Conclusion Evaluation for certain evolving dermoscopic features in melanocytic lesions monitored by SDDI and TBP is efficient in assisting clinical decision making. SDDI with TBP is an effective tool for early detection of melanoma.
doi_str_mv 10.1111/ajd.13975
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Dermoscopic features specific to melanoma have been well described, however, dynamic changes on serial imaging are less understood. This study aims to identify and compare dermoscopic features in developing melanomas and benign naevi that underwent SDDI and TBP to understand which dermoscopic features may be associated with a malignant change. Method Histopathology reports from a private specialist dermatology clinic from January 2007 to December 2019 were reviewed. Histopathologically confirmed melanoma and benign naevi that underwent SDDI and TBP with a minimum follow‐up interval of 3 months were included. Results Eighty‐nine melanomas (38.2% invasive, median Breslow thickness 0.35 mm, range: 0.2–1.45 mm) and 48 benign naevi were evaluated by three experienced dermatologists for dermoscopic changes. Features most strongly associated with melanoma included the development of neovascularisation, asymmetry and growth in pigment network, additional colours, shiny white structures, regression, structureless areas and change to a multi‐component pattern. The presence of atypical vessels (p = 0.02) and shiny white structures (p = 0.02) were significantly associated with invasive melanoma. Conclusion Evaluation for certain evolving dermoscopic features in melanocytic lesions monitored by SDDI and TBP is efficient in assisting clinical decision making. SDDI with TBP is an effective tool for early detection of melanoma.</description><identifier>ISSN: 0004-8380</identifier><identifier>EISSN: 1440-0960</identifier><identifier>DOI: 10.1111/ajd.13975</identifier><identifier>PMID: 36652275</identifier><language>eng</language><publisher>Australia: Wiley Subscription Services, Inc</publisher><subject>Australia ; Benign ; Decision making ; Dermoscopy - methods ; Humans ; Melanoma ; Melanoma - pathology ; Melanoma, Cutaneous Malignant ; Nevus, Pigmented - diagnostic imaging ; Nevus, Pigmented - pathology ; Photography ; Skin Neoplasms - pathology</subject><ispartof>Australasian journal of dermatology, 2023-02, Vol.64 (1), p.67-79</ispartof><rights>2023 The Australasian College of Dermatologists.</rights><rights>Copyright © 2023 The Australasian College of Dermatologists</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3535-f3e0a15d07a721418b2cbd38c621390df19b3e79c9f2256ac835a181081868f03</citedby><cites>FETCH-LOGICAL-c3535-f3e0a15d07a721418b2cbd38c621390df19b3e79c9f2256ac835a181081868f03</cites><orcidid>0000-0001-6988-9555 ; 0000-0002-3357-5826 ; 0000-0002-7210-8884 ; 0000-0002-9497-0504</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2Fajd.13975$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Fajd.13975$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1417,27924,27925,45574,45575</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/36652275$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Nguyen, Jennifer</creatorcontrib><creatorcontrib>Doolan, Brent J</creatorcontrib><creatorcontrib>Pan, Yan</creatorcontrib><creatorcontrib>Vestergaard, Tine</creatorcontrib><creatorcontrib>Paul, Eldho</creatorcontrib><creatorcontrib>McLean, Catriona</creatorcontrib><creatorcontrib>Haskett, Martin</creatorcontrib><creatorcontrib>Kelly, John</creatorcontrib><creatorcontrib>Mar, Victoria</creatorcontrib><creatorcontrib>Chamberlain, Alexander</creatorcontrib><title>Evaluation of dynamic dermoscopic features of melanoma and benign naevi by sequential digital dermoscopic imaging and total body photography in a high‐risk Australian cohort</title><title>Australasian journal of dermatology</title><addtitle>Australas J Dermatol</addtitle><description>Background/Objectives Sequential digital dermoscopic imaging (SDDI) and total body photography (TBP) are recommended as a two‐step surveillance method for individuals at high‐risk of developing cutaneous melanoma. Dermoscopic features specific to melanoma have been well described, however, dynamic changes on serial imaging are less understood. This study aims to identify and compare dermoscopic features in developing melanomas and benign naevi that underwent SDDI and TBP to understand which dermoscopic features may be associated with a malignant change. Method Histopathology reports from a private specialist dermatology clinic from January 2007 to December 2019 were reviewed. Histopathologically confirmed melanoma and benign naevi that underwent SDDI and TBP with a minimum follow‐up interval of 3 months were included. Results Eighty‐nine melanomas (38.2% invasive, median Breslow thickness 0.35 mm, range: 0.2–1.45 mm) and 48 benign naevi were evaluated by three experienced dermatologists for dermoscopic changes. Features most strongly associated with melanoma included the development of neovascularisation, asymmetry and growth in pigment network, additional colours, shiny white structures, regression, structureless areas and change to a multi‐component pattern. The presence of atypical vessels (p = 0.02) and shiny white structures (p = 0.02) were significantly associated with invasive melanoma. Conclusion Evaluation for certain evolving dermoscopic features in melanocytic lesions monitored by SDDI and TBP is efficient in assisting clinical decision making. 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Doolan, Brent J ; Pan, Yan ; Vestergaard, Tine ; Paul, Eldho ; McLean, Catriona ; Haskett, Martin ; Kelly, John ; Mar, Victoria ; Chamberlain, Alexander</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3535-f3e0a15d07a721418b2cbd38c621390df19b3e79c9f2256ac835a181081868f03</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Australia</topic><topic>Benign</topic><topic>Decision making</topic><topic>Dermoscopy - methods</topic><topic>Humans</topic><topic>Melanoma</topic><topic>Melanoma - pathology</topic><topic>Melanoma, Cutaneous Malignant</topic><topic>Nevus, Pigmented - diagnostic imaging</topic><topic>Nevus, Pigmented - pathology</topic><topic>Photography</topic><topic>Skin Neoplasms - pathology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Nguyen, Jennifer</creatorcontrib><creatorcontrib>Doolan, Brent J</creatorcontrib><creatorcontrib>Pan, Yan</creatorcontrib><creatorcontrib>Vestergaard, Tine</creatorcontrib><creatorcontrib>Paul, Eldho</creatorcontrib><creatorcontrib>McLean, Catriona</creatorcontrib><creatorcontrib>Haskett, Martin</creatorcontrib><creatorcontrib>Kelly, John</creatorcontrib><creatorcontrib>Mar, Victoria</creatorcontrib><creatorcontrib>Chamberlain, Alexander</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Immunology Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Australasian journal of dermatology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Nguyen, Jennifer</au><au>Doolan, Brent J</au><au>Pan, Yan</au><au>Vestergaard, Tine</au><au>Paul, Eldho</au><au>McLean, Catriona</au><au>Haskett, Martin</au><au>Kelly, John</au><au>Mar, Victoria</au><au>Chamberlain, Alexander</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Evaluation of dynamic dermoscopic features of melanoma and benign naevi by sequential digital dermoscopic imaging and total body photography in a high‐risk Australian cohort</atitle><jtitle>Australasian journal of dermatology</jtitle><addtitle>Australas J Dermatol</addtitle><date>2023-02</date><risdate>2023</risdate><volume>64</volume><issue>1</issue><spage>67</spage><epage>79</epage><pages>67-79</pages><issn>0004-8380</issn><eissn>1440-0960</eissn><abstract>Background/Objectives Sequential digital dermoscopic imaging (SDDI) and total body photography (TBP) are recommended as a two‐step surveillance method for individuals at high‐risk of developing cutaneous melanoma. Dermoscopic features specific to melanoma have been well described, however, dynamic changes on serial imaging are less understood. This study aims to identify and compare dermoscopic features in developing melanomas and benign naevi that underwent SDDI and TBP to understand which dermoscopic features may be associated with a malignant change. Method Histopathology reports from a private specialist dermatology clinic from January 2007 to December 2019 were reviewed. Histopathologically confirmed melanoma and benign naevi that underwent SDDI and TBP with a minimum follow‐up interval of 3 months were included. Results Eighty‐nine melanomas (38.2% invasive, median Breslow thickness 0.35 mm, range: 0.2–1.45 mm) and 48 benign naevi were evaluated by three experienced dermatologists for dermoscopic changes. Features most strongly associated with melanoma included the development of neovascularisation, asymmetry and growth in pigment network, additional colours, shiny white structures, regression, structureless areas and change to a multi‐component pattern. The presence of atypical vessels (p = 0.02) and shiny white structures (p = 0.02) were significantly associated with invasive melanoma. Conclusion Evaluation for certain evolving dermoscopic features in melanocytic lesions monitored by SDDI and TBP is efficient in assisting clinical decision making. 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subjects Australia
Benign
Decision making
Dermoscopy - methods
Humans
Melanoma
Melanoma - pathology
Melanoma, Cutaneous Malignant
Nevus, Pigmented - diagnostic imaging
Nevus, Pigmented - pathology
Photography
Skin Neoplasms - pathology
title Evaluation of dynamic dermoscopic features of melanoma and benign naevi by sequential digital dermoscopic imaging and total body photography in a high‐risk Australian cohort
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