Lee Young In, Oh Sang Ho
Department of Dermatology, Severance Hospital, Cutaneous Biology Research Institute, Yonsei University College of Medicine, Seoul, Korea.
Ann Dermatol. 2019 Apr;31(2):209-212. doi: 10.5021/ad.2019.31.2.209. Epub 2019 Feb 28.
Symmetrical giant facial plaque-type juvenile xanthogranuloma (SGFP-JXG) is a rare variant of juvenile xanthogranuloma, reported only in two cases in the literature. We report a case of a 3-year-old Korean boy who developed bilateral yellowish indurated plaques on both cheeks since 1 year after birth. A skin biopsy revealed numerous foam cells and Touton type giant cells throughout the upper dermis, and its immunohistochemical studies resulted positive for CD68 and negative for S-100. The boy was therefore diagnosed as a persistent SGFP-JXG. As the lesion did not show any signs of spontaneous regression, we performed a single session of fractional ablative CO laser, which resulted in a significant reduction of the lesion. This is the first case report of a persistent SGFP-JXG on which a single ablative laser therapy was performed with a successful outcome.
对称性巨大面部斑块型幼年性黄色肉芽肿(SGFP-JXG)是幼年性黄色肉芽肿的一种罕见变异型,文献中仅报道过两例。我们报告一例3岁韩国男孩,自出生后1年起双侧脸颊出现淡黄色硬结性斑块。皮肤活检显示整个真皮上层有大量泡沫细胞和图顿型巨细胞,免疫组化研究结果显示CD68阳性,S-100阴性。因此,该男孩被诊断为持续性SGFP-JXG。由于病变未显示任何自发消退迹象,我们进行了单次分次剥脱性CO2激光治疗,病变明显缩小。这是首例对持续性SGFP-JXG进行单次剥脱性激光治疗并取得成功的病例报告。