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Clinicopathologic characteristics of early-onset Becker's nevus in Korean children and adolescents

Authors
Kim, Young J.Roh, Mi RyungLee, Ji HyeNa, Jung ImKo, Joo YeonJung, Joon M.Lee, Jong HeeChang, Sung Eun
Issue Date
Jan-2018
Publisher
WILEY
Citation
INTERNATIONAL JOURNAL OF DERMATOLOGY, v.57, no.1, pp.55 - 61
Indexed
SCIE
SCOPUS
Journal Title
INTERNATIONAL JOURNAL OF DERMATOLOGY
Volume
57
Number
1
Start Page
55
End Page
61
URI
https://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/150736
DOI
10.1111/ijd.13779
ISSN
0011-9059
Abstract
BackgroundBecker's nevus (BN) presents as a hairy patch or plaque with or without proliferation of the dermal smooth muscles. BN has been described as acquired as found in a similar entity, congenital smooth muscle hamartoma (CSMH). This study was aimed at evaluating the clinicopathological aspects of BN in Korean cases in differential diagnosis with CSMH. MethodsWe performed a retrospective study of 103 patients histopathologically diagnosed as having BN or CSMH. The cases included 40 cases diagnosed with BN or CSMH before the age of 10years who had clinical monitoring and a second skin biopsy after puberty to determine the disease course. ResultsAmong cases of children to adolescents (<18years), we observed a slight male predominance. Among children aged <14years, sex ratio converged at 1:1. Early-onset BN showed a female predominance and hyperpigmented skin lesions. All BN cases showed hyperpigmentation, and face and neck involvement tended to make severe cosmetic concerns. In contrast, hypertrichosis was more frequent in CSMH. Either skin-colored lesion or pseudo-Darier's sign was not seen in early-onset BN. BN showed less dermal smooth muscle than CSMH. ConclusionsAndrogens themselves do not seem to be related to the development of BN but play only an aggravating role especially in male patients. Considering high occurrence in exposed areas, BN may distress patients severely. As early laser treatment may be helpful in some patients with BN, early-onset BN in comparison to CSMH should be diagnosed appropriately.
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