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Verfasst von:Tschandl, Philipp [VerfasserIn]   i
 Müller-Christmann, Christine [VerfasserIn]   i
 Hänßle, Holger [VerfasserIn]   i
Titel:Melanomas vs. nevi in high-risk patients under long-term monitoring with digital dermatoscopy
Titelzusatz:do melanomas and nevi already differ at baseline?
Verf.angabe:P. Tschandl, L. Hofmann, C. Fink, H. Kittler, H.A. Haenssle
Jahr:2017
Jahr des Originals:2016
Umfang:6 S.
Fussnoten:Gesehen am 07.09.2018 ; Article was first published on 29 November 2016
Titel Quelle:Enthalten in: European Academy of Dermatology and VenereologyJournal of the European Academy of Dermatology and Venereology
Ort Quelle:Oxford [u.a.] : Wiley-Blackwell, 1991
Jahr Quelle:2017
Band/Heft Quelle:31(2017), 6, Seite 972-977
ISSN Quelle:1468-3083
Abstract:Background: What lesions to select for a most efficient dermatoscopic monitoring of patients with multiple nevi remains an unresolved issue. Objective: To compare the grade of atypia of melanomas and nevi of the same patient at baseline. Methods: Prospective observational study using 236 dermatoscopic baseline images (59 quartets from 59 patients, each including one melanoma detected during follow-up and three nevi). Dermatologists (n = 26) were asked to assess the ‘grade of dermatoscopic atypia’ on a numerical scale and to identify the melanomas. Results: On average, each dermatologist identified 24 of 59 melanomas (40%, range: 11-37). The number of correct picks was greater for dermatologists with moderate (mean: 28) or high (mean: 28) experience compared to beginners (mean 17; P < 0.001). In three of the 59 sets, none of the 26 dermatologists identified the melanoma. The mean grade of dermatoscopic atypia was 2.5 for nevi (95% CI: 2.4-2.6) and 3.0 for melanomas (95% CI: 2.9-3.1, P < 0.001). Limitations: Rating dermatologists were informed that each quartet of images included one melanoma creating substantial deviation from a real-life situation. Conclusion: A significant proportion of melanomas detected during follow-up cannot be differentiated from nevi at baseline. This necessitates the additional inclusion of less atypical lesions for monitoring.
DOI:doi:10.1111/jdv.14065
URL:Bitte beachten Sie: Dies ist ein Bibliographieeintrag. Ein Volltextzugriff für Mitglieder der Universität besteht hier nur, falls für die entsprechende Zeitschrift/den entsprechenden Sammelband ein Abonnement besteht oder es sich um einen OpenAccess-Titel handelt.

Volltext ; Verlag: http://dx.doi.org/10.1111/jdv.14065
 Volltext: https://onlinelibrary.wiley.com/doi/abs/10.1111/jdv.14065
 DOI: https://doi.org/10.1111/jdv.14065
Datenträger:Online-Ressource
Sprache:eng
K10plus-PPN:1580773915
Verknüpfungen:→ Zeitschrift

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