z-logo
Premium
Association of clinicopathological features of melanoma with total naevus count and a history of dysplastic naevi: a cross‐sectional retrospective study within an academic centre
Author(s) -
Tan S. Y.,
Strazzulla L. C.,
Li X.,
Park J. J.,
Lee S.J.,
Kim C. C.
Publication year - 2018
Publication title -
clinical and experimental dermatology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.587
H-Index - 78
eISSN - 1365-2230
pISSN - 0307-6938
DOI - 10.1111/ced.13393
Subject(s) - medicine , breslow thickness , retrospective cohort study , melanoma , biopsy , cross sectional study , dermatology , lesion , nevus , gastroenterology , pathology , cancer , breast cancer , sentinel lymph node , cancer research
Summary Background High naevus count ( HNC ) (≥ 50 naevi) and presence of dysplastic naevi ( DN ) are risk factors for malignant melanoma ( MM ); however, MM s also occur in patients with low naevus count ( LNC ) (< 50 naevi) and in patients without DN . Little is known about differences between MM s in these groups. Aim To characterize the clinicopathological differences between MM s in patients with HNC and those in patients with LNC , with or without biopsy‐proven DN . Methods This was a cross‐sectional retrospective chart review of 281 patients with MM seen between April 2013 and March 2014 at an academic pigmented lesion clinic (Boston, MA , USA ). Results Patients with LNC MM s were diagnosed at an older age (51 vs. 41 years, P < 0.001, OR = 0.95, 95% CI 0.93–0.97), with more aggressive MM features, including greater Breslow thickness (1.1 vs. 0.8 mm, P = 0.01), more mitoses (2 vs. 1 mitoses/mm 2 , P < 0.001), lower rate of superficial spreading subtype (58 vs. 78%, P < 0.01, OR = 2.57, 95% CI 1.31–5.03) and higher MM stage ( P < 0.001), compared to patients with HNC . Patients with DN had similar trends as those in patients with HNC described above, and in addition, were more likely to have a truncal MM (55 vs. 39%, P < 0.01, OR = 1.97, 95% CI 1.22–3.18) with less ulceration (13 vs. 29%, P < 0.01, OR = 0.36, 95% CI 0.19–0.71). Patients without DN were more likely to have a history of a non‐ MM skin cancer (32 vs. 19%, P = 0.01, OR = 0.49, 95% CI 0.28–0.85) and an amelanotic MM (33 vs 21%, P = 0.03, OR = 0.55, 95% CI 0.31–0.96). Conclusions Patients with LNC may develop MM s with more aggressive features at an older age than patients with HNC . A history of biopsy‐proven DN reveals distinct MM differences compared to patients without DN .

This content is not available in your region!

Continue researching here.

Having issues? You can contact us here
Accelerating Research

Address

John Eccles House
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom