Dysplastic nevus syndrome: A phenotypic association of sporadic cutaneous melanoma

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Hereditary dysplastic nevus syndrome: lymphoid cell ultraviolet hypermutability in association with increased melanoma susceptibility.

The hereditary dysplastic nevus syndrome (DNS) is a well-characterized disorder in which affected individuals have increased numbers of premalignant (dysplastic) nevi and a markedly increased risk of developing cutaneous melanoma. Seeking evidence of a systemic disorder in DNS, we examined the effect of ultraviolet radiation on cultured lymphoid cells. Epstein-Barr virus-transformed lymphoblast...

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Dysplastic nevus (atypical nevus).

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Four Cases of Dysplastic Nevus Syndrome

Vol. 26 No. 4, 2014 547 Received June 4, 2013, Revised September 9, 2013, Accepted for publication September 13, 2013 Corresponding author: Seok-Jong Lee, Department of Dermatology, Kyungpook National University Hospital, 130 Dongdeok-ro, Jung-gu, Daegu 700-721, Korea. Tel: 82-53-420-5838, Fax: 82-53-426-0770, E-mail: [email protected] This is an Open Access article distributed under the terms...

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Dysplastic nevus--risk factor or disguise for melanoma.

Dysplastic nevus is an acquired or hereditary nevus that clinically seems atypical and pathohistologically dysplastic. The term of dysplastic nevus has changed through history and even until now the dermatologists and pathologists have not found the same conclusion for name and definition of dysplastic nevus. Epidemiology of dysplastic nevus is different depending on geographic lattitude, being...

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Dysplastic Nevus: A Fake Lesion?

The story of “dysplastic nevus” dates as far back as 1978 when W.H. Clark and colleagues [1] reported a group of melanocytic lesions with atypical clinical and histological features. Such melanocytic nevi were regarded as precursors of melanoma in patients with multiple nevi and/or family history of melanoma and the term of “dysplastic nevus” soon after entered the diagnostic jargon. The concep...

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ژورنال

عنوان ژورنال: Cancer

سال: 1980

ISSN: 0008-543X,1097-0142

DOI: 10.1002/1097-0142(19801015)46:8<1787::aid-cncr2820460816>3.0.co;2-s