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 |
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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 |
format | Article |
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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.</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. SDDI with TBP is an effective tool for early detection of melanoma.</description><subject>Australia</subject><subject>Benign</subject><subject>Decision making</subject><subject>Dermoscopy - methods</subject><subject>Humans</subject><subject>Melanoma</subject><subject>Melanoma - pathology</subject><subject>Melanoma, Cutaneous Malignant</subject><subject>Nevus, Pigmented - diagnostic imaging</subject><subject>Nevus, Pigmented - pathology</subject><subject>Photography</subject><subject>Skin Neoplasms - pathology</subject><issn>0004-8380</issn><issn>1440-0960</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kU9u1DAUhy1ERYfCggsgS2xgkdaOYydZjkr5U1ViA-voxXYSD4kdbKcoO47Qm_ROnARPp0UVEpYlW3qfP_m9H0KvKDmlaZ3BTp1SVpf8CdrQoiAZqQV5ijaEkCKrWEWO0fMQdoRQRjl_ho6ZEDzPS75BtxfXMC4QjbPYdVitFiYjsdJ-ckG6Od07DXHxOuzrkx7BugkwWIVbbU1vsQV9bXC74qB_LNpGAyNWpjdxfz7ymAl6Y_u7p9Htq61TK54HF13vYR5WbCwGPJh--P3rxpvwHW-XED2MBiyWbnA-vkBHHYxBv7w_T9C3Dxdfzz9lV18-fj7fXmWSccazjmkClCtSQpnTglZtLlvFKinyNCiiOlq3TJe1rLs85wJkxTjQipKKVqLqCDtBbw_e2bvUVYjNZILUY2pfuyU0eSlEMpO6TOibf9CdW7xNv0tUKQqSNk_UuwMlvQvB666ZfZqIXxtKmn2KTUqxuUsxsa_vjUs7afWXfIgtAWcH4KcZ9fp_U7O9fH9Q_gHH-qm_</recordid><startdate>202302</startdate><enddate>202302</enddate><creator>Nguyen, Jennifer</creator><creator>Doolan, Brent J</creator><creator>Pan, Yan</creator><creator>Vestergaard, Tine</creator><creator>Paul, Eldho</creator><creator>McLean, Catriona</creator><creator>Haskett, Martin</creator><creator>Kelly, John</creator><creator>Mar, Victoria</creator><creator>Chamberlain, Alexander</creator><general>Wiley Subscription Services, Inc</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7T5</scope><scope>H94</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0001-6988-9555</orcidid><orcidid>https://orcid.org/0000-0002-3357-5826</orcidid><orcidid>https://orcid.org/0000-0002-7210-8884</orcidid><orcidid>https://orcid.org/0000-0002-9497-0504</orcidid></search><sort><creationdate>202302</creationdate><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><author>Nguyen, Jennifer ; 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. SDDI with TBP is an effective tool for early detection of melanoma.</abstract><cop>Australia</cop><pub>Wiley Subscription Services, Inc</pub><pmid>36652275</pmid><doi>10.1111/ajd.13975</doi><tpages>13</tpages><orcidid>https://orcid.org/0000-0001-6988-9555</orcidid><orcidid>https://orcid.org/0000-0002-3357-5826</orcidid><orcidid>https://orcid.org/0000-0002-7210-8884</orcidid><orcidid>https://orcid.org/0000-0002-9497-0504</orcidid><oa>free_for_read</oa></addata></record> |
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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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