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Time to reconsider Spitzoid neoplasms?是时候重新审视Spitzoid肿瘤了吗?
Dermatol Pract Concept. 2016 Apr 30;6(2):43-8. doi: 10.5826/dpc.0602a08. eCollection 2016 Apr.
2
Spitz nevus, Spitz tumor, and spitzoid melanoma: a comprehensive clinicopathologic overview.Spitz 痣、Spitz 瘤和 Spitz 样黑色素瘤:全面的临床病理概述。
Dermatol Clin. 2013 Oct;31(4):589-98, viii. doi: 10.1016/j.det.2013.06.012.
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Analysis of mutations in B-RAF, N-RAS, and H-RAS genes in the differential diagnosis of Spitz nevus and spitzoid melanoma.B-RAF、N-RAS和H-RAS基因变异分析在Spitz痣和Spitzoid黑色素瘤鉴别诊断中的应用
Am J Surg Pathol. 2005 Sep;29(9):1145-51. doi: 10.1097/01.pas.0000157749.18591.9e.
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Genetic similarities between Spitz nevus and Spitzoid melanoma in children.儿童Spitz痣与Spitzoid黑色素瘤之间的遗传相似性。
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Genomic Landscape of Spitzoid Neoplasms Impacting Patient Management.影响患者管理的Spitzoid肿瘤的基因组格局
Front Med (Lausanne). 2018 Dec 13;5:344. doi: 10.3389/fmed.2018.00344. eCollection 2018.
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Surg Pathol Clin. 2009 Sep;2(3):497-510. doi: 10.1016/j.path.2009.08.010. Epub 2009 Oct 29.
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Genomic aberrations in spitzoid melanocytic tumours and their implications for diagnosis, prognosis and therapy.Spitz样黑素细胞肿瘤中的基因组畸变及其对诊断、预后和治疗的意义。
Pathology. 2016 Feb;48(2):113-31. doi: 10.1016/j.pathol.2015.12.007. Epub 2016 Jan 18.
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Atypical Spitz nevi/tumors: lack of consensus for diagnosis, discrimination from melanoma, and prediction of outcome.非典型斯皮茨痣/肿瘤:在诊断、与黑色素瘤的鉴别以及预后预测方面缺乏共识。
Hum Pathol. 1999 May;30(5):513-20. doi: 10.1016/s0046-8177(99)90193-4.
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[Morphological and genetic aspects of Spitz tumors].[斯皮茨瘤的形态学和遗传学方面]
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Loss of p16 expression and copy number changes of CDKN2A in a spectrum of spitzoid melanocytic lesions.一系列Spitz样黑素细胞性病变中p16表达缺失及CDKN2A的拷贝数变化
Hum Pathol. 2016 Dec;58:152-160. doi: 10.1016/j.humpath.2016.07.029. Epub 2016 Aug 26.

引用本文的文献

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Spitz Tumors and Melanoma in the Genomic Age: A Retrospective Look at Ackerman's Conundrum.基因组时代的斯皮茨瘤与黑色素瘤:对阿克曼难题的回顾审视
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Spitz nevus and melanoma: evaluation with dermoscopy and reflectance confocal microscopy.Spitz痣与黑色素瘤:皮肤镜及反射式共聚焦显微镜评估
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3
Spitzoid Neoplasms: Suggestions from Genomic Aberrations.Spitzoid肿瘤:基因组畸变的启示
Dermatopathology (Basel). 2018 Feb 13;5(1):26-29. doi: 10.1159/000486667. eCollection 2018 Jan-Mar.

本文引用的文献

1
Hypopigmented atypical Spitzoid neoplasms (atypical Spitz nevi, atypical Spitz tumors, Spitzoid melanoma): a clinicopathological update.色素减退性非典型Spitz样肿瘤(非典型Spitz痣、非典型Spitz肿瘤、Spitz样黑色素瘤):临床病理进展
Dermatol Pract Concept. 2015 Jan 30;5(1):45-52. doi: 10.5826/dpc.050106. eCollection 2015 Jan.
2
Atypical Spitz tumours and sentinel lymph node biopsy: a systematic review.非典型 Spitz 肿瘤与前哨淋巴结活检:系统评价。
Lancet Oncol. 2014 Apr;15(4):e178-83. doi: 10.1016/S1470-2045(13)70608-9.
3
Kinase fusions are frequent in Spitz tumours and spitzoid melanomas.激酶融合在斯皮茨瘤和斯皮茨样黑色素瘤中很常见。
Nat Commun. 2014;5:3116. doi: 10.1038/ncomms4116.
4
Risk assessment for atypical spitzoid melanocytic neoplasms using FISH to identify chromosomal copy number aberrations.使用 FISH 技术识别染色体拷贝数异常进行非典型 Spitz 样黑素细胞肿瘤的风险评估。
Am J Surg Pathol. 2013 May;37(5):676-84. doi: 10.1097/PAS.0b013e3182753de6.
5
Atypical Spitzoid melanocytic tumors: a morphological, mutational, and FISH analysis.非典型 Spitz 样黑素细胞肿瘤:形态学、突变和 FISH 分析。
J Am Acad Dermatol. 2011 May;64(5):919-35. doi: 10.1016/j.jaad.2010.05.043.
6
Copy number variations and clinical outcome in atypical spitz tumors.非典型 Spitz 肿瘤中的拷贝数变异与临床结局。
Am J Surg Pathol. 2011 Feb;35(2):243-52. doi: 10.1097/PAS.0b013e31820393ee.
7
Melanocytic tumors of uncertain malignant potential: results of a tutorial held at the XXIX Symposium of the International Society of Dermatopathology in Graz, October 2008.交界性黑素细胞肿瘤:2008 年 10 月在格拉茨举行的第 XXIX 届国际皮肤病理学会研讨会的教程结果。
Am J Surg Pathol. 2010 Mar;34(3):314-26. doi: 10.1097/PAS.0b013e3181cf7fa0.
8
Classifying ambiguous melanocytic lesions with FISH and correlation with clinical long-term follow up.应用 FISH 对交界性黑素细胞病变进行分类,并与临床长期随访结果相关联。
Mod Pathol. 2010 Mar;23(3):413-9. doi: 10.1038/modpathol.2009.177. Epub 2010 Jan 15.
9
Fluorescence in situ hybridization (FISH) as an ancillary diagnostic tool in the diagnosis of melanoma.荧光原位杂交(FISH)作为黑色素瘤诊断中的辅助诊断工具。
Am J Surg Pathol. 2009 Aug;33(8):1146-56. doi: 10.1097/PAS.0b013e3181a1ef36.
10
BRAF, NRAS and HRAS mutations in spitzoid tumours and their possible pathogenetic significance.Spitzoid肿瘤中的BRAF、NRAS和HRAS突变及其可能的致病意义。
Br J Dermatol. 2009 Aug;161(2):364-72. doi: 10.1111/j.1365-2133.2009.09181.x. Epub 2009 Apr 29.

是时候重新审视Spitzoid肿瘤了吗?

Time to reconsider Spitzoid neoplasms?

作者信息

Urso Carmelo

机构信息

Department of Anatomic Pathology, Dermatopathology Section, SM Annunziata Hospital, AUSL Toscana Centro, Florence, Italy.

出版信息

Dermatol Pract Concept. 2016 Apr 30;6(2):43-8. doi: 10.5826/dpc.0602a08. eCollection 2016 Apr.

DOI:10.5826/dpc.0602a08
PMID:27222771
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4866626/
Abstract

BACKGROUND

Spitzoid neoplasms may pose significant diagnostic problems because in a fraction of them it is quite difficult or impossible to establish if they are benign or malignant lesions. An extraordinarily large number of studies have been made in attempts to solve this problem; regrettably, the histological criteria proposed and the various special sophisticated techniques employed have proven to be ineffective in making this distinction with confidence.

OBJECTIVES

To explore the possible causes for this diagnostic failure and an attempt to identify the source of this problem.

METHOD

A historical and technical analysis of the specialized literature is performed, critically evaluating the main points of this controversial topic.

RESULTS

The reasons for the diagnostic failure in Spitzoid neoplasms are not clear but could be the result of inappropriate conceptual representation. The analysis of available data and a rational review of old and new assumptions and concepts may suggest a different representation for Spitzoid neoplasms: Spitz nevus, atypical Spitz tumor and Spitzoid melanoma, rather than being three different tumors that are difficult or impossible to distinguish with assurance, could be viewed as one unique entity, Spitz tumor (ST). This tumor is a low-grade malignant neoplasm, in which the amount of intrinsic risk is variable, ranging from very low to high (ST1, ST2, ST3), and malignant potential could be estimated.

CONCLUSIONS

The proposed alternative representation of Spitzoid neoplasms as a unique tumor may help in overcoming the difficulty in diagnosis of these tumors.

摘要

背景

Spitzoid肿瘤可能带来重大的诊断难题,因为其中一部分肿瘤很难甚至无法确定其是良性还是恶性病变。为解决这一问题已经开展了大量研究;遗憾的是,所提出的组织学标准以及采用的各种复杂特殊技术在可靠地区分这些肿瘤方面均被证明是无效的。

目的

探讨这种诊断失败的可能原因,并尝试找出该问题的根源。

方法

对专业文献进行历史和技术分析,批判性地评估这一有争议主题的要点。

结果

Spitzoid肿瘤诊断失败的原因尚不清楚,但可能是概念表述不当所致。对现有数据的分析以及对新旧假设和概念进行合理审视,可能会为Spitzoid肿瘤提出一种不同的表述:Spitz痣、非典型Spitz肿瘤和Spitzoid黑色素瘤,与其被视为三种难以或无法可靠区分的不同肿瘤,不如被看作是一个独特实体,即Spitz肿瘤(ST)。这种肿瘤是一种低级别恶性肿瘤,其内在风险程度各不相同,从非常低到高(ST1、ST2、ST3),并且其恶性潜能是可以估计的。

结论

将Spitzoid肿瘤作为一种独特肿瘤提出替代表述,可能有助于克服这些肿瘤在诊断上的困难。