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原发性皮肤恶性黑色素瘤。

Primary cutaneous malignant melanoma.

作者信息

Maize J C

出版信息

J Am Acad Dermatol. 1983 Jun;8(6):857-63. doi: 10.1016/s0190-9622(83)80017-6.

DOI:10.1016/s0190-9622(83)80017-6
PMID:6345610
Abstract

The prognosis of localized malignant melanoma is related to several histologic features of the primary lesion. Growth pattern, level of invasion, and tumor thickness are currently most widely used in clinical practice, but other features, including ulceration, mitotic rate, density of the inflammatory response, evidence of partial regression, angioinvasion, cell type, cross-sectional profile, and amelanosis have been accorded prognostic significance in single factor analyses. Although stringently controlled prospective studies have yet to demonstrate the validity of these factors for the determination of optimal surgical treatment in individual cases, newer statistical methods of multivariate analysis have made possible assessment of the relative importance of each of these histologic characteristics. The most important and reproducible factor for predicting survival is maximum tumor thickness. Consensus also supports ulceration as another important, independent prognostic indicator, whereas growth pattern and level of invasion derive most of their prognostic value from a secondary correlation with tumor thickness. Mitotic rate may influence survival in the subgroup of patients with high-risk, thick melanomas.

摘要

局限性恶性黑色素瘤的预后与原发灶的若干组织学特征相关。生长方式、浸润深度和肿瘤厚度目前在临床实践中应用最为广泛,但其他特征,包括溃疡形成、有丝分裂率、炎症反应密度、部分消退证据、血管浸润、细胞类型、横断面形态及无黑色素形成,在单因素分析中已被认为具有预后意义。尽管严格对照的前瞻性研究尚未证实这些因素在确定个体病例最佳手术治疗方面的有效性,但更新的多变量分析统计方法已使评估这些组织学特征各自的相对重要性成为可能。预测生存的最重要且可重复的因素是肿瘤最大厚度。共识也支持溃疡形成是另一个重要的独立预后指标,而生长方式和浸润深度的大部分预后价值来自于与肿瘤厚度的次要相关性。有丝分裂率可能影响高危、厚黑色素瘤患者亚组的生存。

相似文献

1
Primary cutaneous malignant melanoma.原发性皮肤恶性黑色素瘤。
J Am Acad Dermatol. 1983 Jun;8(6):857-63. doi: 10.1016/s0190-9622(83)80017-6.
2
The prognostic significance of ulceration of cutaneous melanoma.皮肤黑色素瘤溃疡的预后意义。
Cancer. 1980 Jun 15;45(12):3012-7. doi: 10.1002/1097-0142(19800615)45:12<3012::aid-cncr2820451223>3.0.co;2-o.
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Independent prognostic importance of vascular invasion in nodular melanomas.结节性黑色素瘤中血管侵犯的独立预后重要性。
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Prognostic factors in primary cutaneous malignant melanoma.原发性皮肤恶性黑色素瘤的预后因素
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5
Prognostic subclassifications of T1 cutaneous melanomas based on ulceration, tumour thickness and Clark's level of invasion: results of a population-based study from the Swedish Melanoma Register.基于溃疡、肿瘤厚度和 Clark 浸润深度对 T1 期皮肤黑色素瘤的预后分类:来自瑞典黑色素瘤登记处的一项基于人群的研究结果。
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A retrospective histological study of 669 cases of primary cutaneous malignant melanoma in clinical stage I. 4. The relation of cross-sectional profile, level of invasion, ulceration and vascular invasion to tumour type and prognosis.一项对669例临床I期原发性皮肤恶性黑色素瘤的回顾性组织学研究。4. 横断面形态、浸润深度、溃疡及血管侵犯与肿瘤类型和预后的关系。
Acta Pathol Microbiol Scand A. 1979 Mar;87A(2):131-8.
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Prognostic value of tumour thickness in cutaneous malignant melanoma.肿瘤厚度在皮肤恶性黑色素瘤中的预后价值。
J Clin Pathol. 1983 Jan;36(1):51-6. doi: 10.1136/jcp.36.1.51.
8
Lymphatic invasion identified by monoclonal antibody D2-40, younger age, and ulceration: predictors of sentinel lymph node involvement in primary cutaneous melanoma.通过单克隆抗体D2-40鉴定的淋巴管侵犯、较年轻的年龄以及溃疡:原发性皮肤黑色素瘤前哨淋巴结受累的预测因素。
Arch Dermatol. 2008 Apr;144(4):462-7. doi: 10.1001/archderm.144.4.462.
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Thick cutaneous malignant melanoma: a reappraisal of prognostic factors.厚皮恶性黑色素瘤:预后因素的重新评估。
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10
Depth of invasion and tumor thickness in primary cutaneous malignant melanoma. A study of 2012 cases.原发性皮肤恶性黑色素瘤的浸润深度和肿瘤厚度。一项对2012例病例的研究。
Acta Pathol Microbiol Immunol Scand A. 1985 Mar;93(2):49-55.

引用本文的文献

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Integrated Bioinformatics Analysis Exhibits Pivotal Exercise-Induced Genes and Corresponding Pathways in Malignant Melanoma.综合生物信息学分析揭示了恶性黑色素瘤中关键的运动诱导基因及相应通路。
Front Genet. 2021 Feb 18;11:637320. doi: 10.3389/fgene.2020.637320. eCollection 2020.
2
Tumor cell growth fractions in human malignant melanomas and the correlation to histopathologic tumor grading.人类恶性黑色素瘤中的肿瘤细胞生长分数及其与组织病理学肿瘤分级的相关性。
Am J Pathol. 1989 May;134(5):1063-8.
3
Induction of different morphologic features of malignant melanoma and pigmented lesions after transformation of murine melanocytes with bFGF-cDNA and H-ras, myc, neu, and E1a oncogenes.
用碱性成纤维细胞生长因子(bFGF)-互补脱氧核糖核酸(cDNA)以及H-ras、myc、neu和E1a癌基因转化小鼠黑素细胞后,诱导恶性黑色素瘤和色素沉着病变的不同形态学特征。
Am J Pathol. 1991 Feb;138(2):349-58.