Dermoscopic Features of Melanocytic Nevi in Cardiofaciocutaneous and Costello Syndromes

Author:

Vaughn Alexandra R.1,Meyer Summer N.1,Nazir Zaeem H.2,Tavernetti Jennifer1,Simmons Elanee1,Li Hong3,Rybak Irina1,Rauen Katherine A.4,Marghoob Ashfaq A.2,Kiuru Maija15

Affiliation:

1. Department of Dermatology, University of California Davis School of Medicine, Sacramento

2. Dermatology Service, Memorial Sloan Kettering Cancer Center, Hauppauge, New York

3. Department of Public Health Sciences, University of California Davis School of Medicine, Sacramento

4. Department of Pediatrics, University of California Davis School of Medicine, Sacramento

5. Department of Pathology and Laboratory Medicine, University of California Davis School of Medicine, Sacramento

Abstract

ImportanceSomatic variants in the RAS/MAPK pathway genes are commonly associated with melanocytic nevi and melanoma, whereas germline variants in these genes are associated with RASopathies, syndromes involving multiple organs, including the skin. Nevi counts may be higher in some RASopathies, but studies on features observed through dermoscopy are limited.ObjectiveTo determine the distinguishing dermoscopic features of melanocytic nevi and how the RAS pathway influences them by comparing nevi in patients with cardiofaciocutaneous syndrome (CFC) and Costello syndrome (CS).Design, Setting, and ParticipantsIn this prospective cohort study, patients with CFC and CS, 2 RASopathies caused by variants in the downstream and upstream components of the RAS/MAPK pathway, were recruited from the international CFC and CS family conferences. Some patients with CFC also elected to participate in a longitudinal follow-up study.Main Outcomes and MeasuresThe main outcomes were dermoscopic features and, in the longitudinal follow-up study, nevi counts, which were recorded over time.ResultsA total of 39 patients, 16 with CFC and 23 with CS, were enrolled (overall cohort: 26 [66.7%] female; median [IQR] age, 13.0 [7.6-22.0] years). The 112 nevi overall frequently displayed an organized dermoscopic pattern (CFC, 61 [84.7%]; CS, 34 [85.0%]) rather than a disorganized pattern (CFC, 6 [8.3%]; CS, 1 [2.5%]). Of the organized nevi, homogenous brown was the most common pattern (CFC, 41 [67.2%]; CS, 22 [64.7%]), followed by reticular (CFC, 11 [18.0%]; CS, 7 [20.6%]) and globular (CFC, 9 [14.8%]; CS, 5 [14.7%]). Pigmented networks occurred in 12 nevi in CFC (16.7%) and 6 nevi in CS (15%; P > .99). Of these, 6 CFC-associated nevi (50%) and no CS-associated nevi had atypical networks (P = .05). Six patients with CFC in the follow-up study developed significantly more nevi within 5 years (median [IQR] increase, 24.5 [10-120] nevi; P = .04).Conclusions and RelevanceIn this cohort study, the findings suggest that nevi in patients with CFC and CS commonly display organized homogenous brown dermoscopic patterns, and the number of nevi may significantly increase over time in those with CFC. A disorganized pattern and atypical networks may be more frequent in patients with CFC. Future studies are needed to determine the risk of melanoma in individuals with CFC or CS.

Publisher

American Medical Association (AMA)

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