The Daily Papule

JAADObservational study

Risk-adapted monitoring of melanocytic lesions with peripheral globules

A longitudinal cohort study on melanoma risk stratification.

Gündüz K, Erol Mart HM, Şimşek ÖF, Özsan İ, Günel MD, Öktem A, Akay BN

Journal of the American Academy of DermatologyIn the feed 6 Aug 2026, published online 6 Aug 2026, issue 2026 Aug 06, added to PubMed 6 Aug 2026

Topics: Skin cancer & tumorsMelanoma & molesDermatopathologyImaging, dermoscopy & AI

Abstract

BACKGROUNDPeripheral globules are often considered a marker of benign horizontal growth in melanocytic nevi, but their significance during follow-up remains unclear.

OBJECTIVETo determine whether longitudinal evolution of peripheral globules and related lesion dynamics predict adverse histopathologic outcomes.

METHODSIn this single-center ambispective cohort study, 1923 melanocytic lesions with peripheral globules from 215 patients underwent sequential digital dermoscopy. Longitudinal changes in globules, growth rate, and pigmentation were analyzed using a Bayesian generalized linear mixed model with patient-level random intercepts.

RESULTSDuring follow-up, 46.9% of lesions showed complete globule resolution. Compared with resolution, persistent globules were associated with increased risk, including stable globules (adjusted OR, 3.91; 95% CrI, 1.32-12.21) and increasing globules (adjusted OR, 4.18; 95% CrI, 1.33-13.93). Increasing pigmentation (adjusted OR, 6.33; 95% CrI, 2.39-18.21), faster growth (adjusted OR, 1.15 per 0.1 mm2/month; 95% CrI, 1.04-1.26), and personal history of melanoma (adjusted OR, 7.65; 95% CrI, 2.99-22.02) were independently associated with a clinically significant histopathologic endpoint, whereas age was not.

LIMITATIONSSingle-center design, possible referral bias, and lack of histopathologic confirmation for non-excised lesions.

CONCLUSIONPeripheral globules are dynamic rather than static findings, and longitudinal lesion behavior may improve risk stratification beyond baseline morphology alone.

Abstract from PubMed

PMID 42562098 · DOI 10.1016/j.jaad.2026.08.003

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