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

被引:13
|
作者
Song, J. S. [1 ,2 ,3 ]
London, W. B. [2 ,4 ,5 ]
Hawryluk, E. B. [1 ,2 ,3 ]
Guo, D. [4 ]
Sridharan, M. [4 ]
Fisher, D. E. [2 ,3 ]
Lehmann, L. E. [2 ,4 ,5 ]
Duncan, C. N. [2 ,4 ,5 ]
Huang, J. T. [1 ,2 ,4 ]
机构
[1] Boston Childrens Hosp, Dept Med, Dermatol Program, Fegan 6,300 Longwood Ave, Boston, MA 02115 USA
[2] Harvard Med Sch, Boston, MA USA
[3] Massachusetts Gen Hosp, Dept Dermatol, Boston, MA 02114 USA
[4] Dana Farber Canc Inst, Dept Pediat Oncol, Boston, MA 02115 USA
[5] Boston Childrens Hosp, Dept Med, Div Hematol Oncol, Boston, MA 02115 USA
关键词
BONE-MARROW-TRANSPLANTATION; VERSUS-HOST-DISEASE; POPULATION-BASED COHORT; TOTAL-BODY IRRADIATION; CUTANEOUS MELANOMA; ATOPIC-DERMATITIS; MINOR ANOMALIES; SOLID CANCERS; INCREASED PREVALENCE; MALIGNANT NEOPLASMS;
D O I
10.1038/bmt.2017.57
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
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.
引用
收藏
页码:989 / 997
页数:9
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