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Absence of BRAF and HRAS mutations in eruptive Spitz naevi

  • S Gantner
  • , T Wiesner
  • , L Cerroni
  • , Irene Lurkin
  • , Ellen Zwarthoff
  • , M Landthaler
  • , C Hafner

Research output: Contribution to journalArticleAcademicpeer-review

11 Citations (Scopus)

Abstract

P>Background Eruptive Spitz naevi have been reported rarely in the literature. In solitary Spitz naevi, BRAF and HRAS mutations, as well as increased copy numbers of chromosome 11p have been identified. Objectives To investigate the genetic changes underlying eruptive Spitz naevi. Methods We report on a 16-year-old boy who developed multiple disseminated eruptive Spitz naevi within a few months. We analysed BRAF, HRAS, KRAS and NRAS genes in 39 naevi from this patient for hotspot mutations. Furthermore, comparative genomic hybridization analysis was performed in three lesions. Results None of the Spitz naevi displayed a mutation in the analysed genes, and no chromosomal imbalances were observed. Conclusions Our results indicate that the typical genetic alterations described in solitary Spitz naevi appear to be absent in eruptive Spitz naevi. Yet unknown alternative genetic alterations must account for this rare syndrome.
Original languageUndefined/Unknown
Pages (from-to)873-877
Number of pages5
JournalBritish Journal of Dermatology
Volume164
Issue number4
Publication statusPublished - 2011

Research programs

  • EMC MM-03-24-01

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