CDKN2A and MC1R variants influence dermoscopic and confocal features of benign melanocytic lesions in multiple melanoma patients

Sara Bassoli, Andrea Maurichi, Monica Rodolfo, Alice Casari, Simona Frigerio, Gaia Pupelli, Francesca Farnetani, Giuseppe Pelosi, Mario Santinami, Giovanni Pellacani

Research output: Contribution to journalArticle

18 Citations (Scopus)

Abstract

Non-invasive diagnostic tools are effective in the histomorphological study of melanocytic lesions. The role of melanoma susceptibility genes on melanocytic nevi histopathological features is not clear. The current study aimed to correlate genetic alterations and histomorphological features of melanocytic nevi. Clinical, dermoscopic and confocal features of 34 multiple melanoma patients and 34 controls were compared. Among patients with melanoma, carriers of CDKN2A mutations and/or MC1R variants, and wild-type genes were also compared. In patients with melanoma, a lighter phototype (P = 0.051), a higher number of nevi (P <0.01) and clinically atypical nevi (P <0.01) were observed. At dermoscopy, these nevi showed a complex pattern (P = 0.011), atypical network (P = 0.018) and irregular pigmentation (P = 0.037); at confocal, an irregular meshwork pattern (P = 0.026) with atypical nests (P = 0.016) and an inflammatory infiltrate (P = 0.048) were observed. Among patients with melanoma genetically tested, CDKN2A G101W mutation carriers were more frequently younger (P = 0.023), with clinically atypical nevi (P = 0.050), with cytological atypia (P = 0.033) at confocal. G101W mutation and MC1R variants carriers showed hypopigmented nevi (P = 0.002) and, at confocal, roundish cells infiltrating the junction (P = 0.019). These data suggest an influence of CDKN2A mutation and MC1R variants in the development of dysplastic melanocytic lesions. Non-invasive histomorphological evaluation, together with genetic studies, improves melanoma risk identification and early diagnosis, for a patient-tailored management.

Original languageEnglish
Pages (from-to)411-416
Number of pages6
JournalExperimental Dermatology
Volume22
Issue number6
DOIs
Publication statusPublished - Jun 2013

Fingerprint

Nevus
Melanoma
Genes
Pigmented Nevus
Mutation
Dermoscopy
Intercellular Junctions
Pigmentation
Early Diagnosis

Keywords

  • CDKN2A
  • Confocal microscopy
  • Dermoscopy
  • MC1R
  • Melanocytic nevi
  • Melanoma

ASJC Scopus subject areas

  • Dermatology
  • Molecular Biology
  • Biochemistry

Cite this

CDKN2A and MC1R variants influence dermoscopic and confocal features of benign melanocytic lesions in multiple melanoma patients. / Bassoli, Sara; Maurichi, Andrea; Rodolfo, Monica; Casari, Alice; Frigerio, Simona; Pupelli, Gaia; Farnetani, Francesca; Pelosi, Giuseppe; Santinami, Mario; Pellacani, Giovanni.

In: Experimental Dermatology, Vol. 22, No. 6, 06.2013, p. 411-416.

Research output: Contribution to journalArticle

Bassoli, Sara ; Maurichi, Andrea ; Rodolfo, Monica ; Casari, Alice ; Frigerio, Simona ; Pupelli, Gaia ; Farnetani, Francesca ; Pelosi, Giuseppe ; Santinami, Mario ; Pellacani, Giovanni. / CDKN2A and MC1R variants influence dermoscopic and confocal features of benign melanocytic lesions in multiple melanoma patients. In: Experimental Dermatology. 2013 ; Vol. 22, No. 6. pp. 411-416.
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abstract = "Non-invasive diagnostic tools are effective in the histomorphological study of melanocytic lesions. The role of melanoma susceptibility genes on melanocytic nevi histopathological features is not clear. The current study aimed to correlate genetic alterations and histomorphological features of melanocytic nevi. Clinical, dermoscopic and confocal features of 34 multiple melanoma patients and 34 controls were compared. Among patients with melanoma, carriers of CDKN2A mutations and/or MC1R variants, and wild-type genes were also compared. In patients with melanoma, a lighter phototype (P = 0.051), a higher number of nevi (P <0.01) and clinically atypical nevi (P <0.01) were observed. At dermoscopy, these nevi showed a complex pattern (P = 0.011), atypical network (P = 0.018) and irregular pigmentation (P = 0.037); at confocal, an irregular meshwork pattern (P = 0.026) with atypical nests (P = 0.016) and an inflammatory infiltrate (P = 0.048) were observed. Among patients with melanoma genetically tested, CDKN2A G101W mutation carriers were more frequently younger (P = 0.023), with clinically atypical nevi (P = 0.050), with cytological atypia (P = 0.033) at confocal. G101W mutation and MC1R variants carriers showed hypopigmented nevi (P = 0.002) and, at confocal, roundish cells infiltrating the junction (P = 0.019). These data suggest an influence of CDKN2A mutation and MC1R variants in the development of dysplastic melanocytic lesions. Non-invasive histomorphological evaluation, together with genetic studies, improves melanoma risk identification and early diagnosis, for a patient-tailored management.",
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