{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2023,9,11]],"date-time":"2023-09-11T20:54:38Z","timestamp":1694465678425},"reference-count":10,"publisher":"Wiley","issue":"5","license":[{"start":{"date-parts":[[2018,12,13]],"date-time":"2018-12-13T00:00:00Z","timestamp":1544659200000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"}],"content-domain":{"domain":["onlinelibrary.wiley.com"],"crossmark-restriction":true},"short-container-title":["Int J Dermatology"],"published-print":{"date-parts":[[2019,5]]},"abstract":"<jats:title>Abstract<\/jats:title><jats:sec><jats:title>Background<\/jats:title><jats:p>A significant number of pigmented lesions are biopsied to rule out melanoma, but most will be benign. MelaFind<jats:styled-content style=\"fixed-case\"><jats:sup>TM<\/jats:sup><\/jats:styled-content> is a highly sensitive, noninvasive computer\u2010assisted system to aid in clinical diagnosis of melanoma.<\/jats:p><\/jats:sec><jats:sec><jats:title>Methods<\/jats:title><jats:p>A total of 140 high\u2010risk patients were followed by one expert dermatologist. Biopsies were blindly and independently evaluated by two dermatopathologists and given histologic severity scores (<jats:styled-content style=\"fixed-case\">HSS<\/jats:styled-content>, 0\u201312) based on the histologic features of melanoma\/dysplastic nevi and compared to pathologic diagnoses and MelaFind<jats:styled-content style=\"fixed-case\"><jats:sup>TM<\/jats:sup><\/jats:styled-content> scores.<\/jats:p><\/jats:sec><jats:sec><jats:title>Results<\/jats:title><jats:p>MelaFind<jats:styled-content style=\"fixed-case\"><jats:sup>TM<\/jats:sup><\/jats:styled-content> reduced the biopsy number of clinically ambiguous lesions (923 scanned to 253 biopsied, 73% reduction). Biopsied cases were usually benign (135\/253, 53.4%, <jats:styled-content style=\"fixed-case\">HSS<\/jats:styled-content> = 2.8\u20133.2). Dysplastic nevi with varying degrees of atypia were observed next most commonly (80\/253, 31.6%, <jats:styled-content style=\"fixed-case\">HSS<\/jats:styled-content> = 4.7\u20135.2 for mild dysplasia and 7\u20137.6 for moderate to severe dysplasia). Melanomas comprised 11\/253 (4.3%) of biopsies (<jats:styled-content style=\"fixed-case\">HSS<\/jats:styled-content> = 9.3\u201310.7). Twenty\u2010four cases were given miscellaneous diagnoses not within the dysplastic nevus\u2013melanoma spectrum (9.5%, <jats:styled-content style=\"fixed-case\">HSS<\/jats:styled-content> = 1.3). Dermal fibrosis was the most commonly identified worrisome histologic feature (177\/253, 70%), closely followed by other known atypical features. Nonthreatening histologic features in benign lesions with high MelaFind<jats:styled-content style=\"fixed-case\"><jats:sup>TM<\/jats:sup><\/jats:styled-content> disorganization scores were common. The <jats:styled-content style=\"fixed-case\">HSS<\/jats:styled-content> differed significantly depending on pathologic diagnosis severity, while the MelaFind<jats:styled-content style=\"fixed-case\"><jats:sup>TM<\/jats:sup><\/jats:styled-content> score did not (benign = 2.2; mildly atypical = 4.8; moderately to severely atypical = 2.3; in\u2010situ or invasive melanoma = 3.1).<\/jats:p><\/jats:sec><jats:sec><jats:title>Conclusions<\/jats:title><jats:p>MelaFind<jats:styled-content style=\"fixed-case\"><jats:sup>TM<\/jats:sup><\/jats:styled-content> unequivocally reduced the number of biopsies, but banal lesions had histologic attributes resulting in high\u2010risk MelaFind<jats:styled-content style=\"fixed-case\"><jats:sup>TM<\/jats:sup><\/jats:styled-content> scores, and MelaFind<jats:styled-content style=\"fixed-case\"><jats:sup>TM<\/jats:sup><\/jats:styled-content> does not correlate with degree of cytologic atypia. Knowledge of these limitations should increase bidirectional confidence when making clinicopathologic correlations in high\u2010risk patients.<\/jats:p><\/jats:sec>","DOI":"10.1111\/ijd.14336","type":"journal-article","created":{"date-parts":[[2018,12,14]],"date-time":"2018-12-14T06:50:43Z","timestamp":1544770243000},"page":"569-576","update-policy":"http:\/\/dx.doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":3,"title":["Histopathologic correlation of high\u2010risk MelaFind<sup>TM<\/sup> lesions: a 3\u2010year experience from a high\u2010risk pigmented lesion clinic"],"prefix":"10.1111","volume":"58","author":[{"given":"Vikas","family":"Shrivastava","sequence":"first","affiliation":[{"name":"Department of Dermatology Naval Medical Center Portsmouth Portsmouth VA USA"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Phillip","family":"Bailin","sequence":"additional","affiliation":[{"name":"Dermatology and Plastic Surgery Institute Cleveland Clinic Cleveland OH USA"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Jennifer","family":"Elliott","sequence":"additional","affiliation":[{"name":"Dermatology and Plastic Surgery Institute Cleveland Clinic Cleveland OH USA"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Elizabeth","family":"Bacnik","sequence":"additional","affiliation":[{"name":"Dermatology and Plastic Surgery Institute Cleveland Clinic Cleveland OH USA"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Brian","family":"Gastman","sequence":"additional","affiliation":[{"name":"Dermatology and Plastic Surgery Institute Cleveland Clinic Cleveland OH USA"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Wilma","family":"Bergfeld","sequence":"additional","affiliation":[{"name":"Dermatology and Plastic Surgery Institute Cleveland Clinic Cleveland OH USA"},{"name":"Pathology and Laboratory Medicine Institute Cleveland OH USA"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Steven D.","family":"Billings","sequence":"additional","affiliation":[{"name":"Dermatology and Plastic Surgery Institute Cleveland Clinic Cleveland OH USA"},{"name":"Pathology and Laboratory Medicine Institute Cleveland OH USA"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Melissa","family":"Piliang","sequence":"additional","affiliation":[{"name":"Dermatology and Plastic Surgery Institute Cleveland Clinic Cleveland OH USA"},{"name":"Pathology and Laboratory Medicine Institute Cleveland OH USA"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Anthony","family":"Fernandez","sequence":"additional","affiliation":[{"name":"Dermatology and Plastic Surgery Institute Cleveland Clinic Cleveland OH USA"},{"name":"Pathology and Laboratory Medicine Institute Cleveland OH USA"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Ivanka","family":"Kovalyshyn","sequence":"additional","affiliation":[{"name":"US Path Labs Boca Raton FL USA"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Jennifer S.","family":"Ko","sequence":"additional","affiliation":[{"name":"Dermatology and Plastic Surgery Institute Cleveland Clinic Cleveland OH USA"},{"name":"Pathology and Laboratory Medicine Institute Cleveland OH USA"}],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"311","published-online":{"date-parts":[[2018,12,13]]},"reference":[{"key":"e_1_2_5_2_1","doi-asserted-by":"publisher","DOI":"10.1016\/j.jaad.2008.10.065"},{"key":"e_1_2_5_3_1","doi-asserted-by":"publisher","DOI":"10.1016\/j.jaad.2016.02.1152"},{"key":"e_1_2_5_4_1","unstructured":"NeighmondP.Doctors question rise in skin cancer biopsies.NPR. 03 May 2007. 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