TY - JOUR
T1 - Nonmalignant late cutaneous changes after allogeneic hematopoietic stem cell transplant in children
AU - Huang, Jennifer T.
AU - Song, Johanna S.
AU - Hawryluk, Elena B.
AU - London, Wendy B.
AU - Guo, Dongjing
AU - Sridharan, Madhumitha
AU - Fisher, David E.
AU - Lehmann, Leslie E.
AU - Duncan, Christine N.
N1 - Funding Information:
Supported in part by a Pilot Project Grant by the Society for Pediatric Dermatology and by a Career Development Award by the Dermatology Foundation.
Publisher Copyright:
© 2018 American Academy of Dermatology, Inc.
PY - 2018/8
Y1 - 2018/8
N2 - Background: There are limited pediatric data on nonmalignant cutaneous changes, including autoimmune conditions and permanent alopecia, after hematopoietic stem cell transplantation (HSCT). Objective: We sought to characterize late cutaneous changes and associated risk factors after allogeneic HSCT in children. Methods: A cross-sectional cohort study of pediatric HSCT recipients was performed at a single institution. All participants underwent a full skin examination. Results: The median visit age was 13.8 years, with a median time post-HSCT of 3.6 years. Of 85 patients, 14% (n = 12) had vitiligo, 16% (n = 14) had psoriasis/sebopsoriasis, 25% (n = 21) had alopecia, and 6% (n = 5) had nail changes. Factors significantly associated with vitiligo included a history of chronic graft-versus-host disease (cGVHD), transplant indication of primary immunodeficiency, and younger age at transplant (<10 years of age). Fifty-two percent of patients with alopecia had androgenetic alopecia patterns. Factors significantly associated with alopecia included cGVHD, busulfan conditioning, and family history of early male pattern alopecia. All patients with nail changes had cGVHD. Limitations: The cross-sectional design did not allow time of onset identification. Histopathologic correlation was not performed. Conclusion: Pediatric HSCT recipients, particularly those with cGVHD, are at risk for developing nonmalignant late cutaneous changes.
AB - Background: There are limited pediatric data on nonmalignant cutaneous changes, including autoimmune conditions and permanent alopecia, after hematopoietic stem cell transplantation (HSCT). Objective: We sought to characterize late cutaneous changes and associated risk factors after allogeneic HSCT in children. Methods: A cross-sectional cohort study of pediatric HSCT recipients was performed at a single institution. All participants underwent a full skin examination. Results: The median visit age was 13.8 years, with a median time post-HSCT of 3.6 years. Of 85 patients, 14% (n = 12) had vitiligo, 16% (n = 14) had psoriasis/sebopsoriasis, 25% (n = 21) had alopecia, and 6% (n = 5) had nail changes. Factors significantly associated with vitiligo included a history of chronic graft-versus-host disease (cGVHD), transplant indication of primary immunodeficiency, and younger age at transplant (<10 years of age). Fifty-two percent of patients with alopecia had androgenetic alopecia patterns. Factors significantly associated with alopecia included cGVHD, busulfan conditioning, and family history of early male pattern alopecia. All patients with nail changes had cGVHD. Limitations: The cross-sectional design did not allow time of onset identification. Histopathologic correlation was not performed. Conclusion: Pediatric HSCT recipients, particularly those with cGVHD, are at risk for developing nonmalignant late cutaneous changes.
KW - alopecia
KW - autoimmune
KW - hematopoietic stem cell transplant
KW - pediatric
KW - vitiligo
UR - http://www.scopus.com/inward/record.url?scp=85046813605&partnerID=8YFLogxK
U2 - 10.1016/j.jaad.2018.03.029
DO - 10.1016/j.jaad.2018.03.029
M3 - Article
C2 - 29588248
AN - SCOPUS:85046813605
SN - 0190-9622
VL - 79
SP - 230
EP - 237
JO - Journal of the American Academy of Dermatology
JF - Journal of the American Academy of Dermatology
IS - 2
ER -