» Articles » PMID: 33205467

Association Between the Dermoscopic Morphology of Peripheral Globules and Melanocytic Lesion Diagnosis

Overview
Date 2020 Nov 18
PMID 33205467
Citations 3
Authors
Affiliations
Soon will be listed here.
Abstract

Background: The presence of peripheral globules is associated with enlarging melanocytic lesions; however, there are numerous patterns of peripheral globules distribution and it remains unknown whether specific patterns can help differentiate enlarging naevi from melanoma.

Objective: To investigate whether morphological differences exist between the peripheral globules seen in different subsets of naevi and in melanoma.

Methods: A cross-sectional study of clinical notes that mentioned peripheral globules, in addition to all melanoma images with peripheral globules on the International Skin Imaging Collaboration archive. Dermoscopic images were reviewed and annotated. Associations between diagnosis and categorical features were measured with odds ratios. Non-parametric tests were used for continuous factors.

Results: 184 lesions with peripheral globules from our clinic were included in the analysis; only 6 of these proved to be melanoma. 109 melanomas with peripheral globules from the International Skin Imaging Collaboration archive were added to the analysis. Melanomas were more common on the extremities and among older individuals. Melanomas were more likely to display atypical, tiered and/or focal peripheral globules. Only 5% of melanomas lacked dermoscopic melanoma-specific structures compared to 48% of naevi.

Conclusions: Melanocytic lesions with atypical or asymmetrically distributed peripheral globules, especially when located on the extremities, should raise suspicion for malignancy. Melanocytic lesions with typical and symmetrically distributed peripheral globules, and with no other concerning dermoscopic features, are unlikely to be malignant.

Citing Articles

Dermoscopic monitoring of pediatric melanocytic nevi regarding pattern and diameter changes.

Erdil D, Aksu A, Turgut Erdemir V, Erdil D, Leblebici C, Kara Polat A An Bras Dermatol. 2024; 99(6):833-839.

PMID: 39004596 PMC: 11551263. DOI: 10.1016/j.abd.2024.01.004.


Melanocytic Lesions with Peripheral Globules: Proposal of an Integrated Management Algorithm.

Cappilli S, Ribero S, Cornacchia L, Catapano S, Del Regno L, Quattrini L Dermatol Pract Concept. 2023; 13(1).

PMID: 36892354 PMC: 9946096. DOI: 10.5826/dpc.1301a10.


Dermoscopic Criteria, Histopathological Correlates and Genetic Findings of Thin Melanoma on Non-Volar Skin.

Massone C, Hofman-Wellenhof R, Chiodi S, Sola S Genes (Basel). 2021; 12(8).

PMID: 34440462 PMC: 8391530. DOI: 10.3390/genes12081288.

References
1.
Zalaudek I, Docimo G, Argenziano G . Using dermoscopic criteria and patient-related factors for the management of pigmented melanocytic nevi. Arch Dermatol. 2009; 145(7):816-26. PMC: 2856040. DOI: 10.1001/archdermatol.2009.115. View

2.
Kittler H, Pehamberger H, Wolff K, Binder M . Follow-up of melanocytic skin lesions with digital epiluminescence microscopy: patterns of modifications observed in early melanoma, atypical nevi, and common nevi. J Am Acad Dermatol. 2000; 43(3):467-76. DOI: 10.1067/mjd.2000.107504. View

3.
Xu J, Gupta K, V Stoecker W, Krishnamurthy Y, Rabinovitz H, Bangert A . Analysis of globule types in malignant melanoma. Arch Dermatol. 2009; 145(11):1245-51. PMC: 3161409. DOI: 10.1001/archdermatol.2009.285. View

4.
Scope A, Marchetti M, Marghoob A, Dusza S, Geller A, Satagopan J . The study of nevi in children: Principles learned and implications for melanoma diagnosis. J Am Acad Dermatol. 2016; 75(4):813-823. PMC: 5030195. DOI: 10.1016/j.jaad.2016.03.027. View

5.
Bajaj S, Dusza S, Marchetti M, Wu X, Fonseca M, Kose K . Growth-Curve Modeling of Nevi With a Peripheral Globular Pattern. JAMA Dermatol. 2015; 151(12):1338-1345. PMC: 5483973. DOI: 10.1001/jamadermatol.2015.2231. View