Department of Dermatology, Hôpital Robert Debré, 51092 Reims, France.
Br J Dermatol. 2012 Apr;166(4):727-39. doi: 10.1111/j.1365-2133.2011.10772.x.
While early recognition and prognosis of melanoma as a whole have improved, particular forms of rarer, under-recognized or more severe tumours require increasing attention. Among them, melanomas located on the hand and/or foot (hand and foot melanoma, HFM) have been the subject of few and heterogeneous studies, with variable and sometimes confusing results, and have not been targeted to date by comprehensive literature reviews.
To perform a formal, systematic review of the literature, focusing on epidemiology, risk factors, prognosis and genetic characteristics of HFM. Methods All data sources were identified through searches on Medline, Scopus and Cochrane databases. Articles were selected and evaluated according to predefined quality criteria.
Among 1185 articles screened for relevance, 37 met the inclusion criteria. Data analysis brought to light important particularities of HFMs: they are rare in all ethnic groups of developed countries, but have been insufficiently studied in the developing world. About half are of the specific acral lentiginous melanoma (ALM) subtype. Previous trauma and naevi on the soles/toes were identified as two main risk factors in case-control studies. Genetic or environmental factors other than sun exposure are likely to play a role but require further investigation. Compared with melanoma at other sites, their prognosis is poor mainly as a consequence of later diagnosis, but possibly also because of an intrinsic negative effect of the HFM/ALM subtype. Standard prognostic factors of melanoma have been insufficiently validated to date in HFM. Finally, their molecular genetic particularities could lead to specific targeted therapies in the near future.
Overall, HFM could represent a particular subgroup of rare, potentially severe melanomas, requiring specific management from their prevention up to their treatment.
虽然整体上黑素瘤的早期识别和预后有所改善,但某些形式的罕见、认识不足或更严重的肿瘤需要越来越多的关注。其中,位于手和/或脚的黑素瘤(手部和足部黑素瘤,HFM)的研究较少且具有异质性,结果也各不相同,甚至有时相互矛盾,迄今为止尚未有全面的文献综述对其进行针对性研究。
对 HFM 的流行病学、危险因素、预后和遗传特征进行正式的系统综述。
通过在 Medline、Scopus 和 Cochrane 数据库中进行检索,确定所有数据来源。根据预先设定的质量标准选择和评估文章。
在筛选出的 1185 篇相关文章中,有 37 篇符合纳入标准。数据分析揭示了 HFM 的一些重要特点:它们在所有发达国家的种族中都很罕见,但在发展中国家研究不足。大约一半为特定的肢端雀斑样黑素瘤(ALM)亚型。既往创伤和足底/脚趾的痣被认为是病例对照研究中的两个主要危险因素。除了阳光暴露之外,遗传或环境因素可能发挥作用,但需要进一步研究。与其他部位的黑素瘤相比,HFM 的预后较差,主要是由于诊断较晚,但也可能是由于 HFM/ALM 亚型的内在负面影响。迄今为止,标准的黑素瘤预后因素在 HFM 中尚未得到充分验证。最后,它们的分子遗传特征可能导致未来不久就能采用特定的靶向治疗。
总的来说,HFM 可能代表一组罕见的、潜在严重的黑素瘤,从预防到治疗都需要有特定的管理方法。