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异基因造血干细胞移植后儿童患黑素细胞痣和非黑素瘤皮肤癌的风险。

Risk of melanocytic nevi and nonmelanoma skin cancer in children after allogeneic hematopoietic stem cell transplantation.

作者信息

Song J S, London W B, Hawryluk E B, Guo D, Sridharan M, Fisher D E, Lehmann L E, Duncan C N, Huang J T

机构信息

Department of Medicine, Dermatology Program, Boston Children's Hospital, Boston, MA, USA.

Harvard Medical School, Boston, MA, USA.

出版信息

Bone Marrow Transplant. 2017 Jul;52(7):989-997. doi: 10.1038/bmt.2017.57. Epub 2017 Apr 3.

DOI:10.1038/bmt.2017.57
PMID:28368380
Abstract

There is a known increased risk of skin cancer in the adult population after hematopoietic stem cell transplantation (HSCT). However, late dermatologic effects that children may experience after HSCT have not been well described. The primary objective of this study was to characterize nevi and skin cancers affecting children after allogeneic HSCT. A cross-sectional cohort study of 85 pediatric HSCT recipients and 85 controls matched for age, sex and skin phototype was performed at a single institution. All participants underwent a full skin examination. Median age at study visit was 13.8 years in HSCT patients with median time post-HSCT of 3.6 years. HSCT patients had significantly more nevi than control patients (median (range): 44 (0-150) vs 11 (0-94), P<0.0001). HSCT patients also had significantly more nevi >5 mm in diameter and atypical nevi than controls. Factors associated with increased nevus count included malignant indication for HSCT, pretransplant chemotherapy, TBI exposure and myeloablative conditioning. A total of 16.5% of HSCT patients developed cancerous, precancerous lesions and/or lentigines. Our study suggests that pediatric HSCT recipients have an increased risk of benign and atypical melanocytic proliferations and nonmelanoma skin cancer that can manifest even during childhood.

摘要

已知造血干细胞移植(HSCT)后成年人群患皮肤癌的风险会增加。然而,儿童HSCT后可能出现的晚期皮肤影响尚未得到充分描述。本研究的主要目的是描述异基因HSCT后影响儿童的痣和皮肤癌。在一家机构对85名儿科HSCT受者和85名年龄、性别和皮肤光型相匹配的对照进行了一项横断面队列研究。所有参与者都接受了全面的皮肤检查。HSCT患者研究访视时的中位年龄为13.8岁,HSCT后的中位时间为3.6年。HSCT患者的痣明显多于对照患者(中位数(范围):44(0 - 150)对11(0 - 94),P<0.0001)。HSCT患者直径>5毫米的痣和非典型痣也明显多于对照。与痣数量增加相关的因素包括HSCT的恶性指征、移植前化疗、TBI暴露和清髓性预处理。共有16.5%的HSCT患者发生了癌性、癌前病变和/或雀斑样痣。我们的研究表明,儿科HSCT受者患良性和非典型黑素细胞增殖以及非黑素瘤皮肤癌的风险增加,甚至在儿童期就可能出现。

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与背景人群和肾移植受者相比,造血干细胞移植受者的皮肤癌风险:一项基于人群的队列研究。
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