Absence of BRAF and HRAS mutations in eruptive Spitz naevi

Summary 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  W...

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Veröffentlicht in:British journal of dermatology (1951) 2011-04, Vol.164 (4), p.873-877
Hauptverfasser: Gantner, S., Wiesner, T., Cerroni, L., Lurkin, I., Zwarthoff, E.C., Landthaler, M., Hafner, C.
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Sprache:eng
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Zusammenfassung:Summary 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.
ISSN:0007-0963
1365-2133
DOI:10.1111/j.1365-2133.2011.10210.x