TITLE:
Non-Invasive Evaluation and Differential Diagnosis for Pediatric Leukoderma in a Single Institute
AUTHORS:
Madoka Takafuji, Atsushi Tanemura, Yuma Hanaoka, Noriko Arase, Eiji Kiyohara, Ichiro Katayama, Manabu Fujimoto
KEYWORDS:
Pediatric Leukoderma, Vitiligo, Nevus Depigmentosus, Non-Invasive Diagnosis, Wood’s Lamp
JOURNAL NAME:
Journal of Cosmetics, Dermatological Sciences and Applications,
Vol.9 No.4,
November
29,
2019
ABSTRACT: Background: Although vitiligo shows a similar clinical picture to other disorders in which patients exhibit depigmented spots, there are few reports on the differentiation of these conditions from each other. Purpose: We aimed to investigate the differences and similarities between vitiligo and nevus depigmentosus in children based on the clinical course and characteristics. Materials and Methods: We conducted an examination of the disease type, treatment, progress, and differentiation of 85 cases of vitiligo and nevus depigmentosus that developed before 15 years of age among patients who visited the Osaka University Department of Dermatology with a chief complaint of white patches from January 2010 to March 2017. Results: The median age at the onset of symptoms of 79 patients with vitiligo was 4.5 years and while that of 6 patients with nevus depigmentosus was 0.8 years, indicating that the onset of nevus depigmentosus occurred earlier. While vitiligo often developed in the head and neck regions, with a tendency for depigmented spots in multiple regions, nevus depigmentosus did not show this tendency in these regions. Upon performing Wood’s lamp observation in 38 cases of vitiligo, 35 cases were found to be fluorescent chalky white and in 3 cases histologically diagnosed as vitiligo, no clear fluorescent color was observed. All 6 patients diagnosed with nevus depigmentosus exhibited a non-fluorescent off-white color under a Wood’s lamp. Conclusions: This study indicates that non-invasive observation using a Wood’s lamp is useful in the differential diagnosis of pediatric leukoderma, in addition to the subsequent clinical course, such as the presence or absence of lesional repigmentation and/or enlargement.