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侵袭性结节性黑色素瘤:伴有罕见BRAF突变的病例报告

Aggressive nodular melanoma: case report with an unusual BRAF mutation.

作者信息

El Bardai Sanae, El Agy Fatima, Mernissi Fatima Zahra, Kamal Dounia, Tahiri Elousrouti Layla, Chbani Laila, Hammas Nawal

机构信息

High Institute of Nursing Professions and Health Techniques, Fez, Morocco.

Biomedical and Translational Research Laboratory, Faculty of Medicine and Pharmacy, Sidi Mohamed Ben Abdallah University, Fez, Morocco.

出版信息

Mol Biol Rep. 2025 Jul 9;52(1):688. doi: 10.1007/s11033-025-10803-w.

Abstract

BACKGROUND

Nodular melanoma (NM) is considered one of the most aggressive forms of skin cancer, accounting for approximately 10-15% of all melanoma cases. It tends to grow quickly and spread deeper into the skin's layers, providing fewer opportunities for early detection. NM often carries a poor prognosis due to local invasion and frequent distant metastases. BRAF mutations are frequently found in melanoma, with the most common mutation being a single-point mutation at codon 600 (typically V600E).

CASE PRESENTATION

We report a case of aggressive jugal nodular melanoma harboring an unusual BRAF mutation, C. 1789_1790 CT>TC.

METHODS

Genomic DNA was extracted from formalin-fixed paraffin-embedded (FFPE) tumor tissue. Sanger sequencing was employed to analyze exon 15 of the BRAF gene. The mutation was validated by bidirectional sequencing and interpreted using reference databases.

RESULTS

The identified BRAF mutation, c.1789_1790CT>TC, has been rarely reported in the literature. It results in a non-canonical amino acid substitution, potentially affecting kinase activity and therapeutic response.

CONCLUSION

This case underscores the clinical and molecular heterogeneity of nodular melanoma and highlights the importance of comprehensive BRAF mutation screening beyond the common V600E variant.

摘要

背景

结节性黑色素瘤(NM)被认为是皮肤癌中侵袭性最强的类型之一,约占所有黑色素瘤病例的10%-15%。它往往生长迅速,且会更深地扩散至皮肤各层,导致早期检测的机会较少。由于局部侵袭和频繁的远处转移,NM的预后通常较差。BRAF突变在黑色素瘤中经常被发现,最常见的突变是密码子600处的单点突变(通常为V600E)。

病例报告

我们报告一例侵袭性颊部结节性黑色素瘤病例,该病例携带一种不寻常的BRAF突变,即C. 1789_1790 CT>TC。

方法

从福尔马林固定石蜡包埋(FFPE)肿瘤组织中提取基因组DNA。采用Sanger测序法分析BRAF基因的第15外显子。通过双向测序验证该突变,并使用参考数据库进行解读。

结果

所鉴定出的BRAF突变c.1789_1790CT>TC在文献中鲜有报道。它导致一种非典型氨基酸替代,可能影响激酶活性和治疗反应。

结论

该病例强调了结节性黑色素瘤的临床和分子异质性,并突出了除常见的V600E变异之外进行全面BRAF突变筛查的重要性。

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