Development of Dysplastic Nevi in a Child with LEPR Deficiency Treated with Setmelanotide.

J Clin Res Pediatr Endocrinol

Division of Pediatric Endocrinology, Department of Pediatrics, Faculty of Medicine, Uludağ University, Bursa, Türkiye.

Published: August 2025


Category Ranking

98%

Total Visits

921

Avg Visit Duration

2 minutes

Citations

20

Article Abstract

Setmelanotide is a recently approved medication for patients over two years of age with monogenic obesity that emerges from POMC, LEPR, PCSK1 mutations, or Bardet-Biedl syndrome. While primarily targeting melanocortin-4 receptors (MC4R), setmelanotide also weakly stimulates melanocortin-1 receptors (MC1R), which may affect pigmentation. Clinical outcomes of this treatment modality remain limited due to the rarity of disorders mentioned above. We present a 12-year-old boy with a homozygous LEPR mutation who experienced skin hyperpigmentation shortly after the initiation of setmelanotide treatment. By the third month of treatment, gradual darkening of nevi was noted. At six-month follow-up, two nevi were excised due to pigmentation changes, and histopathology revealed dysplastic features in both. This case raises concerns about potential MC1R-mediated melanocytic activity during setmelanotide treatment. Therapy was temporarily discontinued. To our knowledge, this is the first reported pediatric case with LEPR-related monogenic obesity developing dysplastic nevi during setmelanotide use.

Download full-text PDF

Source
http://dx.doi.org/10.4274/jcrpe.galenos.2025.2025-5-14DOI Listing

Publication Analysis

Top Keywords

dysplastic nevi
8
monogenic obesity
8
setmelanotide treatment
8
setmelanotide
6
development dysplastic
4
nevi
4
nevi child
4
child lepr
4
lepr deficiency
4
deficiency treated
4

Similar Publications

Background: The 23-gene expression signature (GES) assay (myPath Melanoma) is a well-established molecular test for analyzing challenging melanocytic lesions, alongside fluorescence in situ hybridization (FISH) and single nucleotide polymorphism (SNP) array. However, routine use of these tests is often limited by high costs, long turnaround times, significant tissue requirements, and limited accessibility. This study aimed to evaluate the diagnostic concordance of PRAME immunohistochemistry (IHC) and the GES assay in difficult melanocytic lesions to determine whether PRAME IHC, widely available in pathology laboratories, could serve as a surrogate for GES.

View Article and Find Full Text PDF

Background: Fingolimod was approved in 2010 for the treatment of relapsing-remitting multiple sclerosis, generally as second-line therapy. While its efficacy in reducing the relapse rate is well-recognized, the dermatologic complications of fingolimod remain unexplored. Herein, we aimed to report our experience with multiple sclerosis patients treated with fingolimod who underwent periodic dermatologic examinations.

View Article and Find Full Text PDF

Development of Dysplastic Nevi in a Child with LEPR Deficiency Treated with Setmelanotide.

J Clin Res Pediatr Endocrinol

August 2025

Division of Pediatric Endocrinology, Department of Pediatrics, Faculty of Medicine, Uludağ University, Bursa, Türkiye.

Setmelanotide is a recently approved medication for patients over two years of age with monogenic obesity that emerges from POMC, LEPR, PCSK1 mutations, or Bardet-Biedl syndrome. While primarily targeting melanocortin-4 receptors (MC4R), setmelanotide also weakly stimulates melanocortin-1 receptors (MC1R), which may affect pigmentation. Clinical outcomes of this treatment modality remain limited due to the rarity of disorders mentioned above.

View Article and Find Full Text PDF