[Skip to Content]
Access to paid content on this site is currently suspended due to excessive activity being detected from your IP address 54.197.90.95. Please contact the publisher to request reinstatement.
[Skip to Content Landing]
Article
August 1994

Familial Site-Specific Congenital Melanocytic Nevus: Report of Two Families

Author Affiliations

Departments of Dermatology and Pediatrics University of California 400 Parnassus Ave Box 0316 San Francisco, CA 94143-0316

Arch Dermatol. 1994;130(8):1075-1076. doi:10.1001/archderm.1994.01690080145029
Abstract

Small and intermediate-sized congenital melanocytic nevi (CMN) are relatively common birthmarks, occurring in approximately 1% of the population. The presence of small CMN as a familial trait has seldom been reported.1 We describe two families in which a grandparent and grandchild each had an intermediate-sized congenital melanocytic nevus at the identical site on the body.

Report of Cases.  Case 1. An 8-month-old infant was referred for evaluation of an intermediate-sized congenital melanocytic nevus present on the right forearm, without significant change since birth. The family of this infant was particularly concerned about this birthmark because her 47-year-old maternal grandmother had a CMN located in the identical location since birth. Shortly after the birth of her granddaughter, the grandmother's nevus began to change in color and become more elevated (Figure). This lesion, measuring 3X2.8 cm, was excised and found to be a malignant melanoma, Clark's level 2, invasive to 0.4

First Page Preview View Large
First page PDF preview
First page PDF preview
×