The Cutaneous Evolution of Nevi in a Patient with Familial, Atypical, Multiple‐mole Melanoma Syndrome

Henry T. Lynch; Ramon M. Fusaro; Calvin L. Treger; Judith Pester; Jane F. Lynch

doi:10.1111/j.1525-1470.1985.tb00467.x

The Cutaneous Evolution of Nevi in a Patient with Familial, Atypical, Multiple‐mole Melanoma Syndrome

Henry T. Lynch, Ramon M. Fusaro, Calvin L. Treger, Judith Pester, Jane F. Lynch

Department of Preventive Medicine

Research output: Contribution to journal › Article

14 Scopus citations

Abstract

For almost two decades we have followed a kindred with the familial, atypical, multiple-mole melanoma (FAMMM) syndrome. We first evaluated the proband's 14-year-old daughter when she was age 5 years. We documented the evolution, both clinically and histologically, of the FAMMM phenotype in this girl for eight years.

Original language	English (US)
Pages (from-to)	289-293
Number of pages	5
Journal	Pediatric Dermatology
Volume	2
Issue number	4
DOIs	https://doi.org/10.1111/j.1525-1470.1985.tb00467.x
State	Published - Jul 1985

All Science Journal Classification (ASJC) codes

Pediatrics, Perinatology, and Child Health
Dermatology

Access to Document

10.1111/j.1525-1470.1985.tb00467.x

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Lynch, H. T., Fusaro, R. M., Treger, C. L., Pester, J., & Lynch, J. F. (1985). The Cutaneous Evolution of Nevi in a Patient with Familial, Atypical, Multiple‐mole Melanoma Syndrome. Pediatric Dermatology, 2(4), 289-293. https://doi.org/10.1111/j.1525-1470.1985.tb00467.x

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