用Setmelanotide治疗LEPR缺乏症儿童的发育不良痣。

IF 1.5 4区 医学 Q4 ENDOCRINOLOGY & METABOLISM
Hatice Nursoy, Yasemin Denkboy Öngen, Ferdi Öztürk, Şaduman Balaban Adım, Erdal Eren
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引用次数: 0

摘要

Setmelanotide是最近批准的一种药物,用于两岁以上由POMC、LEPR、PCSK1突变或Bardet-Biedl综合征引起的单基因肥胖患者。setmelanotide主要靶向黑色素皮质素-4受体(melanocortin-4 receptor, MC4R),同时也弱刺激黑色素皮质素-1受体(melanocortin-1 receptor, MC1R),这可能影响色素沉着。由于上述疾病的罕见性,这种治疗方式的临床结果仍然有限。我们提出了一个12岁的男孩与纯合子LEPR突变谁经历皮肤色素沉着后不久开始塞特黑肽治疗。在治疗的第三个月,痣逐渐变黑。在6个月的随访中,由于色素沉着改变,切除了两个痣,组织病理学显示两个痣都有发育不良的特征。该病例引起了对setmelanotide治疗期间mc1r介导的黑素细胞活性的关注。治疗暂时停止。据我们所知,这是首次报道的儿童lepr相关单基因肥胖在使用赛特黑肽期间发生发育不良痣的病例。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Development of Dysplastic Nevi in a Child with LEPR Deficiency Treated with Setmelanotide.

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.

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来源期刊
Journal of Clinical Research in Pediatric Endocrinology
Journal of Clinical Research in Pediatric Endocrinology ENDOCRINOLOGY & METABOLISM-PEDIATRICS
CiteScore
3.60
自引率
5.30%
发文量
73
审稿时长
20 weeks
期刊介绍: The Journal of Clinical Research in Pediatric Endocrinology (JCRPE) publishes original research articles, reviews, short communications, letters, case reports and other special features related to the field of pediatric endocrinology. JCRPE is published in English by the Turkish Pediatric Endocrinology and Diabetes Society quarterly (March, June, September, December). The target audience is physicians, researchers and other healthcare professionals in all areas of pediatric endocrinology.
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