Charcot-Marie-Tooth Disease and Multiple Malignant Melanomas: A Case Report
February 2010 | Volume 9 | Issue 2 | Case Reports | 164 | Copyright © February 2010
Ritu Saini MD, Stephanie Lehrhoff MD, Deborah S. Sarnoff MD
Abstract
The incidence of malignant melanoma has reached more than 62,000 people this past year alone. Much is unknown about the genetic
predisposition of this cancer. The authors present a 62-year-old woman with a history of Charcot-Marie-Tooth disease (CMTD),
diagnosed at age five, who has also developed multiple primary cutaneous malignant melanomas since 2003. The patient presented
to the authors’ clinic with a pigmented lesion on the left thigh, which was increasing in size and changing color. The patient was
diagnosed with malignant melanoma in situ on biopsy. As both CMTD and malignant melanoma are neural crest derived disorders,
this may suggest a shared underlying genetic defect. A gene locus of particular interest is 1p36, both previously recognized in the
proposed pathogenesis of CMTD and malignant melanoma (MM).