[Skip to Content]
Access to paid content on this site is currently suspended due to excessive activity being detected from your IP address Please contact the publisher to request reinstatement.
[Skip to Content Landing]
January 2004

Neonatal Giant Congenital Nevi With Proliferative Nodules: A Clinicopathologic Study and Literature Review of Neonatal Melanoma

Author Affiliations

From the Departments of Dermatology and Pathology, Royal Victoria Infirmary, Newcastle upon Tyne (Drs Leech, Leonard, and Lawrence), and Royal Liverpool University Hospital, Liverpool (Drs Bell and Geurin), and Dermatology, Ninewells Hospital, Dundee (Dr Jones), United Kingdom; Division of Dermatopathology, Department of Pathology, Brigham and Women's Hospital, Boston, Mass (Dr McKee). The authors have no relevant financial interest in this article.

Arch Dermatol. 2004;140(1):83-88. doi:10.1001/archderm.140.1.83

Background  Review of the literature reveals that congenital malignant melanoma is an exceptionally rare occurrence and has a generally poor prognosis when it does occur. However, benign proliferative melanocytic lesions are known to occur within giant congenital nevi (GCN). This entity is not well recognized and can be confused clinically and histologically with malignant change.

Observations  We report 2 cases of GCN in neonates demonstrating benign proliferating nodules present at birth. An initial diagnosis of malignant melanoma was assumed in both cases. Careful histologic analysis, however, revealed these lesions to be benign, as did long-term follow-up of 3.5 years, with both patients remaining well with no evidence of melanoma. Review of the literature suggests that there are 2 clinical patterns of these benign nodules arising within GCNs: small (<1 cm) and large (>1 cm) dermal nodules with varying histologic patterns that we have attempted to categorize.

Conclusions  Our cases illustrate the difficulty in accurate diagnosis of melanocytic lesions in the neonate. We recommend caution in making a diagnosis of malignant melanoma and highlight the possibilty that benign lesions can be mistaken for melanoma in this age group. We encourage the acquisition of fixed histologic specimens for accurate diagnosis of melanocytic lesions.