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儿童非典型黑素细胞肿瘤前哨淋巴结活检:一家机构24例患者的经验

Sentinel node biopsy in atypical melanocytic neoplasms in childhood: a single institution experience in 24 patients.

作者信息

Mills Omie L, Marzban Suroosh, Zager Jonathan S, Sondak Vernon K, Messina Jane L

机构信息

Department of Pathology and Cell Biology, College of Medicine, University of South Florida, Tampa, FL 33612, USA.

出版信息

J Cutan Pathol. 2012 Mar;39(3):331-6. doi: 10.1111/j.1600-0560.2011.01853.x.

Abstract

INTRODUCTION

Sentinel lymph node biopsy (SLNB) is a controversial but frequently used adjunct to wide excision of difficult-to-diagnose melanocytic proliferations of childhood. We herein report our institutional experience with SLNB in pediatric patients with these lesions, hereafter referred to as 'atypical melanocytic proliferations'.

METHODS

Our prospectively collected melanoma database was queried for patients ≤21 years of age status post-SLNB for a diagnosis of atypical melanocytic proliferation in which the diagnosis of melanoma ≥1 mm in depth was considered in the differential diagnosis by one or more expert dermatopathologists and for which no diagnostic consensus could be reached.

RESULTS

Of 24 patients identified over 17 years, 7 patients (29%) had a positive sentinel lymph node (SLN). Six SLN-positive patients underwent complete lymph node dissection, with one (14%) having additional nodal involvement identified. With a median follow-up of 4.1 years (range < 0.1 to 14.8 years), all patients showed no evidence of disease.

CONCLUSIONS

Despite a significant rate of identification of melanocytes in SLNs of children with atypical melanocytic proliferations, survival appears favorable and controversy surrounding the significance of nodal involvement remains. Further studies with larger numbers of patients and long-term follow-up are needed before the true prognostic value of SLNB in this setting can be determined.

摘要

引言

前哨淋巴结活检(SLNB)是一种存在争议但常用于儿童难以诊断的黑素细胞增殖性病变广泛切除的辅助手段。我们在此报告我们机构对患有这些病变(以下称为“非典型黑素细胞增殖”)的儿科患者进行前哨淋巴结活检的经验。

方法

我们前瞻性收集的黑色素瘤数据库中查询了年龄≤21岁、接受前哨淋巴结活检后诊断为非典型黑素细胞增殖的患者,其中一名或多名专家皮肤病理学家在鉴别诊断中考虑深度≥1mm的黑色素瘤诊断,且未达成诊断共识。

结果

在17年期间确定的24例患者中,7例(29%)前哨淋巴结(SLN)阳性。6例SLN阳性患者接受了完整的淋巴结清扫,其中1例(14%)发现有额外的淋巴结受累。中位随访4.1年(范围<0.1至14.8年),所有患者均无疾病证据。

结论

尽管在患有非典型黑素细胞增殖的儿童的前哨淋巴结中发现黑素细胞的比例很高,但生存率似乎良好,围绕淋巴结受累意义的争议仍然存在。在确定前哨淋巴结活检在这种情况下的真正预后价值之前,需要对更多患者进行进一步研究并进行长期随访。

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