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皮肤黑色素瘤的组织病理学亚型:预后及分子学意义

Histopathological Subtypes of Cutaneous Melanoma: Prognostic and Molecular Implications.

作者信息

Qasim Hussein, Abu Shugaer Mohammad, Khattab Karis, Leoni Matteo Luigi Giuseppe, Varrassi Giustino

机构信息

Department of Pathology and Laboratory Medicine, Jordan University of Science and Technology, Irbid, JOR.

Department of Pathology, Jordan University of Science and Technology, Irbid, JOR.

出版信息

Cureus. 2025 Aug 21;17(8):e90670. doi: 10.7759/cureus.90670. eCollection 2025 Aug.

Abstract

Cutaneous melanoma is a biologically diverse and clinically aggressive malignancy with distinct histopathological subtypes that significantly influence its diagnosis, prognosis, and management. This comprehensive review explores the major melanoma subtypes, superficial spreading, nodular, lentigo maligna, acral lentiginous, and desmoplastic melanoma, along with rarer variants such as spitzoid, nevoid, and mucosal melanomas. Each subtype exhibits unique morphological characteristics, growth patterns, anatomical distribution, and molecular profiles, including variations in key mutations such as B-Raf proto-oncogene, serine/threonine kinase (BRAF), KIT proto-oncogene receptor tyrosine kinase (KIT), Neuroblastoma RAS viral oncogene homolog (NRAS), and Neurofibromin 1 (NF1). While histologic subtype is not incorporated into formal staging systems, it frequently correlates with tumor behavior and patient outcomes, guiding surgical planning and adjuvant therapy decisions. Advances in immunohistochemistry, molecular diagnostics, and genomic profiling have refined melanoma classification and opened new avenues for targeted and immune-based therapies. However, diagnostic challenges persist due to overlapping features and under-characterization of rare variants. This review underscores the need for a multimodal approach that integrates histopathologic, molecular, and clinical data to achieve precise classification and optimize patient care in the era of personalized oncology.

摘要

皮肤黑色素瘤是一种生物学特性多样且临床侵袭性强的恶性肿瘤,具有不同的组织病理学亚型,这些亚型对其诊断、预后和治疗有显著影响。本综述全面探讨了黑色素瘤的主要亚型,包括浅表扩散型、结节型、恶性雀斑样痣型、肢端雀斑样痣型和促纤维增生性黑色素瘤,以及罕见的变异型,如Spitz样、痣样和黏膜黑色素瘤。每种亚型都具有独特的形态特征、生长模式、解剖分布和分子特征,包括关键突变的差异,如B-Raf原癌基因、丝氨酸/苏氨酸激酶(BRAF)、KIT原癌基因受体酪氨酸激酶(KIT)、神经母细胞瘤RAS病毒癌基因同源物(NRAS)和神经纤维瘤蛋白1(NF1)。虽然组织学亚型未纳入正式的分期系统,但它通常与肿瘤行为和患者预后相关,指导手术规划和辅助治疗决策。免疫组织化学、分子诊断和基因组分析的进展完善了黑色素瘤的分类,并为靶向治疗和免疫治疗开辟了新途径。然而,由于特征重叠和罕见变异的特征描述不足,诊断挑战依然存在。本综述强调了采用多模式方法的必要性,该方法整合组织病理学、分子和临床数据,以在个性化肿瘤学时代实现精确分类并优化患者护理。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/71ba/12450496/1051ef714983/cureus-0017-00000090670-i01.jpg

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