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肢端雀斑样痣黑色素瘤:126例临床预后研究

Acral lentiginous melanoma: a clinicoprognostic study of 126 cases.

作者信息

Phan A, Touzet S, Dalle S, Ronger-Savlé S, Balme B, Thomas L

机构信息

Department of Dermatology, Hôtel Dieu, Claude Bernard University, 69288 Lyon cedex 02, France.

出版信息

Br J Dermatol. 2006 Sep;155(3):561-9. doi: 10.1111/j.1365-2133.2006.07368.x.

Abstract

BACKGROUND

Although the histopathological subtype of melanoma has not been clearly proven to carry independent prognostic significance, acral lentiginous melanoma (ALM) seems to confer a poorer prognosis mainly because disease is often more advanced at the time of diagnosis.

OBJECTIVES

To investigate the distinctive epidemiological and clinical characteristics of ALM, a peculiar histological entity, and to identify prognostic factors.

METHODS

We performed a register-based review of cases from a single large referral centre, the University Hospital Department of Dermatology, Lyons, France. We reviewed patient demographics, the initial presentation of the lesion, and clinical outcome. ALM-specific and disease-free survival were estimated using the KaplanMeier method and compared using the log-rank test. A Cox model was used to identify prognostic factors.

RESULTS

One hundred and twenty-six patients were identified as having histopathology-proven ALM in our melanoma patient register from 1996 to 2004. There were 46 (37%) subungual ALM and 80 (63%) ALM on soles, palms and nonvolar sites. The mean age at diagnosis was 63 years. There were 44 (35%) men and 82 (65%) women, sex ratio M/F 1 : 1.86. The mean Breslow thickness was 2.51 mm (range: in situ to 20 mm). There was no evidence of overexposure to ultraviolet radiation, nor was there found a predisposing genetic trait. Only 16 (13%) patients recalled a history of trauma. Thirty-four ALM (28%) were unpigmented. The median ALM-specific and disease-free survival were 13.5 and 10.1 years, respectively. The 5-year survival rate was 76%. Multivariate analysis identified tumour thickness, male gender and amelanosis as independent clinical prognostic factors for both ALM-specific and disease-free survival.

CONCLUSIONS

Our study provides specific information on the clinical characteristics and outcome of this uncommon histological subtype of melanoma. However, the pathogenesis remains unknown. Breslow thickness, male gender and amelanosis were significantly associated with a poorer prognosis.

摘要

背景

尽管黑色素瘤的组织病理学亚型尚未被明确证实具有独立的预后意义,但肢端雀斑样痣黑色素瘤(ALM)似乎预后较差,主要原因是在诊断时疾病往往处于更晚期阶段。

目的

研究特殊组织学类型的ALM独特的流行病学和临床特征,并确定预后因素。

方法

我们对来自法国里昂大学医院皮肤科这一大型单一转诊中心的病例进行了基于登记册的回顾。我们回顾了患者的人口统计学资料、病变的初始表现以及临床结局。使用Kaplan-Meier方法估计ALM特异性生存率和无病生存率,并使用对数秩检验进行比较。使用Cox模型确定预后因素。

结果

在我们1996年至2004年的黑色素瘤患者登记册中,有126例患者经组织病理学证实患有ALM。其中46例(37%)为甲下ALM,80例(63%)为足底、手掌和非掌侧部位的ALM。诊断时的平均年龄为63岁。男性44例(35%),女性82例(65%),性别比M/F为1 : 1.86。平均Breslow厚度为2.51 mm(范围:原位至20 mm)。没有证据表明存在紫外线过度暴露,也未发现易患遗传特征。只有16例(13%)患者回忆有创伤史。34例(28%)ALM无色素沉着。ALM特异性生存率和无病生存率的中位数分别为13.5年和10.1年。5年生存率为76%。多变量分析确定肿瘤厚度、男性性别和无色素沉着是ALM特异性生存率和无病生存率的独立临床预后因素。

结论

我们的研究提供了关于这种罕见组织学亚型黑色素瘤的临床特征和结局的具体信息。然而,其发病机制仍然未知。Breslow厚度、男性性别和无色素沉着与较差的预后显著相关。

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