Literature DB >> 32692047

Congenital melanocytic nevi.

Danna Moustafa1, Andrew R Blundell, Elena B Hawryluk.   

Abstract

PURPOSE OF REVIEW: To update pediatric providers on new developments in our understanding of the clinical presentation, genetics, and systemic risks associated with congenital melanocytic nevi (CMN). RECENT
FINDINGS: CMN are primarily caused by sporadic postzygotic somatic mutations, most frequently in NRAS, and studies of the genetic underpinnings of CMN have demonstrated a diverse array of genetic drivers. The primary complications of large and giant CMN include neurocutaneous melanocytosis and malignant melanoma. Abnormalities in CNS MRI may predict a worse clinical course for patients and increased risk of melanoma. Targeted therapies of the MEK pathway have begun to be studied for the treatment of CMN and prevention of associated complications.
SUMMARY: Patients with large and giant CMN should be managed by an interdisciplinary care team for the monitoring of dermatologic, neurologic, and psychosocial concerns. Ongoing research is underway to better characterize the genetic drivers of CMN and to better guide development of targeted therapeutics.

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Year:  2020        PMID: 32692047     DOI: 10.1097/MOP.0000000000000924

Source DB:  PubMed          Journal:  Curr Opin Pediatr        ISSN: 1040-8703            Impact factor:   2.856


  3 in total

1.  Giant Congenital Melanocytic Nevus in a Chinese Newborn.

Authors:  Weizhao Lin; Yixuan Zhou; Ruiman Li
Journal:  Clin Cosmet Investig Dermatol       Date:  2021-05-26

2.  Giant Congenital Melanocytic Nevi in a Pakistani Newborn.

Authors:  Hina Mumtaz Hashmi; Nazia Shamim; Vinod Kumar; Sidra Idrees
Journal:  Cureus       Date:  2021-05-24

Review 3.  Epidemiology of Melanoma.

Authors:  Kalyan Saginala; Adam Barsouk; John Sukumar Aluru; Prashanth Rawla; Alexander Barsouk
Journal:  Med Sci (Basel)       Date:  2021-10-20
  3 in total

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