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黑色和棕色口腔颌面部黏膜皮肤肿瘤

Black and Brown Oro-facial Mucocutaneous Neoplasms.

作者信息

Natarajan Easwar

机构信息

Section of Oral and Maxillofacial Pathology, University of Connecticut Health Center, 263 Farmington Ave, MC-0925, Farmington, CT, 06030, USA.

出版信息

Head Neck Pathol. 2019 Mar;13(1):56-70. doi: 10.1007/s12105-019-01008-2. Epub 2019 Jan 29.

DOI:10.1007/s12105-019-01008-2
PMID:30693458
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6406009/
Abstract

Black and brown-colored mucocutaneous lesions present a differential diagnostic challenge, with malignant melanoma being the primary clinical concern. The vast majority of pigmented lesions in the head and neck region are the result of benign, reactive factors such as post-inflammatory melanosis. However, it is not uncommon to discover a range of muco-cutaneous black and brown neoplasms in the oro-facial area. The majority of black/brown pigmented neoplasms are melanocytic in origin; these are neoplasms of neural crest derivation. Melanocytic nevi are a diverse group of benign neoplasms that are the result of specific oncogenic mutations. They are common on cutaneous surfaces but can manifest in mucosal sites. Currently, nevi are classified based on clinical and histological criteria. The most common cutaneous and oral mucosal nevus is the acquired melanocytic nevus; nevi do not pose an increased risk for the development of malignant melanoma. Emerging information on specific genetic differences supports the notion of biologically distinct nevi. This article will review the classic clinical and microscopic features of nevi commonly found in the head and neck region, and discuss emerging concepts in nevus pathogenesis and taxonomy. Melanoma is a malignant melanocytic neoplasm and is a result of cumulative genetic deregulation. The etiology of malignant melanoma (MM) is multifactorial and includes underlying genetic susceptibility, UV radiation, skin-type, and race. The majority of MM occurs on cutaneous surfaces and less commonly on mucosal and extra-cutaneous visceral organs. Regardless of location, MM exhibits clinical-pathological features that relate to horizontal or vertical tumor spread. Cutaneous and mucosal MM typically present as asymmetrical, irregularly bordered, large (> 0.5 cm), heterogeneous brown-black lesions with foci of erythema, atrophy or ulceration. As with melanocytic nevi, advances in melanomagenesis research have revealed primary oncogenic BRAF and NRAS mutations associated with cutaneous MM. Unlike their cutaneous counterparts, mucosal melanomas exhibit primary oncogenic alterations in c-KIT and other genes. This article will discuss the role of specific primary oncogenic and secondary/tertiary genetic defects in differential clinical presentation, anatomic distribution, future classification changes, and targeted therapy of melanoma. The clinical and microscopic features of mucosal melanomas and a summary of management guidelines will be discussed. Additionally, this article will cover the salient features of melanocytic neuroectodermal tumor of infancy, a neoplastic entity that can involve the oro-facial region, and the clinical-pathological features of selected, commonly occurring pigmented ectodermally-derived neoplasms that are often part of the clinical differential diagnosis of black-brown pigmented lesions.

摘要

黑色和棕色的黏膜皮肤病变带来了鉴别诊断方面的挑战,其中恶性黑色素瘤是主要的临床关注点。头颈部区域的绝大多数色素沉着病变是由良性反应性因素引起的,如炎症后黑变病。然而,在口面部区域发现一系列黏膜皮肤黑色和棕色肿瘤的情况并不少见。大多数黑色/棕色色素沉着肿瘤起源于黑素细胞;这些是神经嵴衍生的肿瘤。黑素细胞痣是一组多样的良性肿瘤,是特定致癌突变的结果。它们在皮肤表面很常见,但也可出现在黏膜部位。目前,痣是根据临床和组织学标准进行分类的。最常见的皮肤和口腔黏膜痣是获得性黑素细胞痣;痣不会增加恶性黑色素瘤发生的风险。关于特定基因差异的新信息支持了生物学上不同的痣这一概念。本文将回顾头颈部区域常见痣的经典临床和微观特征,并讨论痣发病机制和分类学中的新观念。黑色素瘤是一种恶性黑素细胞肿瘤,是累积性基因失调的结果。恶性黑色素瘤(MM)的病因是多因素的,包括潜在的遗传易感性、紫外线辐射、皮肤类型和种族。大多数MM发生在皮肤表面,较少发生在黏膜和皮肤外的内脏器官。无论位置如何,MM都表现出与肿瘤水平或垂直扩散相关的临床病理特征。皮肤和黏膜MM通常表现为不对称、边界不规则、大(>0.5cm)、异质性棕黑色病变,伴有红斑、萎缩或溃疡灶。与黑素细胞痣一样,黑色素瘤发生机制研究的进展揭示了与皮肤MM相关的主要致癌BRAF和NRAS突变。与皮肤黑素瘤不同,黏膜黑色素瘤在c-KIT和其他基因中表现出主要致癌改变。本文将讨论特定主要致癌和二级/三级基因缺陷在黑色素瘤不同临床表现、解剖分布、未来分类变化及靶向治疗中的作用。还将讨论黏膜黑色素瘤的临床和微观特征以及管理指南的总结。此外,本文将涵盖婴儿黑素细胞神经外胚层肿瘤的显著特征,这是一种可累及口面部区域的肿瘤实体,以及一些常见的色素性外胚层来源肿瘤的临床病理特征,这些肿瘤常是黑棕色色素沉着病变临床鉴别诊断的一部分。

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