Your browser doesn't support javascript.
loading
Risk of melanocytic nevi and nonmelanoma skin cancer in children after allogeneic hematopoietic stem cell transplantation.
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.
Affiliation
  • Song JS; Department of Medicine, Dermatology Program, Boston Children's Hospital, Boston, MA, USA.
  • London WB; Harvard Medical School, Boston, MA, USA.
  • Hawryluk EB; Department of Dermatology, Massachusetts General Hospital, Boston, MA, USA.
  • Guo D; Harvard Medical School, Boston, MA, USA.
  • Sridharan M; Department of Pediatric Oncology, Dana-Farber Cancer Institute, Boston, MA, USA.
  • Fisher DE; Department of Medicine, Division of Hematology/Oncology, Boston Children's Hospital, Boston, MA, USA.
  • Lehmann LE; Department of Medicine, Dermatology Program, Boston Children's Hospital, Boston, MA, USA.
  • Duncan CN; Harvard Medical School, Boston, MA, USA.
  • Huang JT; Department of Dermatology, Massachusetts General Hospital, Boston, MA, USA.
Bone Marrow Transplant ; 52(7): 989-997, 2017 Jul.
Article in En | MEDLINE | ID: mdl-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.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Skin Neoplasms / Neoplasms, Second Primary / Hematopoietic Stem Cell Transplantation / Nevus, Pigmented Type of study: Etiology_studies / Observational_studies / Prevalence_studies / Risk_factors_studies Limits: Adolescent / Child / Child, preschool / Female / Humans / Infant / Male Language: En Journal: Bone Marrow Transplant Year: 2017 Document type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Skin Neoplasms / Neoplasms, Second Primary / Hematopoietic Stem Cell Transplantation / Nevus, Pigmented Type of study: Etiology_studies / Observational_studies / Prevalence_studies / Risk_factors_studies Limits: Adolescent / Child / Child, preschool / Female / Humans / Infant / Male Language: En Journal: Bone Marrow Transplant Year: 2017 Document type: Article