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Giant Congenital Melanocytic Nevi: An Update and Emerging Therapies
Girish Gulab Meshram1, Neeraj Kaur2, Kanwaljeet Singh Hura3
1aDepartment of Pharmacology, Postgraduate Institute of Medical Education and Research and Dr. Ram Manohar Lohia Hospital, New Delhi, India.
Abstract:
Giant congenital melanocytic nevi (GCMN) are a rare occurrence. Gain-of-function mutation in the NRAS gene is found to be associated with GCMN, causing abnormal proliferation of embryonic melanoblasts. The two major complications associated with GCMN are malignant melanoma and neurocutaneous melanosis. Treatment of GCMN has conventionally been surgical. However, the role of NRAS inhibitors and inactivation of nevus tissue by high hydrostatic pressure are being explored. We present a case of a 1-day-old neonate born with GCMN, along with a review of the literature.
Insights
Giant congenital melanocytic nevi (GCMN), a rare condition, are linked to NRAS gene mutations causing abnormal melanoblast growth. Potential new treatments beyond surgery are being investigated for these challenging birthmarks.
Area of Science:
- Dermatology
- Genetics
- Pediatrics
Background:
- Giant congenital melanocytic nevi (GCMN) are rare skin conditions present at birth.
- A gain-of-function mutation in the NRAS gene is associated with GCMN development.
- GCMN carries risks of malignant melanoma and neurocutaneous melanosis.
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