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Giant congenital juvenile xanthogranuloma

机译:巨大的先天性青少年肉芽肿性肉芽肿

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A 1-month-old otherwise healthy girl was referred to our clinic for evaluation of a congenital asymptomatic lesion on the face. Upon physical exam, a firm, sharply marginated, infiltrative, yellowish plaque measuring 6x4 cms with peau d'orange surface was evident on the right mandibular region (figure 1). A 4 mm punch biopsy was performed and histological exam revealed a diffuse infiltrate of non-foamy mononuclear histio-cytes with scattered eosinophils within the papillary dermis, and a scarce amount of Touton cells. Immunohistochemistry was positive for the histiocytic marker, CD68, and negative for CD la and S-100 protein, indicating an origin of non-Langerhans cells. On this basis, we confirmed the clinical suspicion of giant congenital juvenile xanthogranuloma (JXG).
机译:一名其他健康的1个月大女孩被转诊至我们的诊所,以评估面部先天性无症状病变。体格检查后,在右下颌区域明显可见坚硬,边缘清晰,浸润的淡黄色斑块,表面呈棕褐色,表面为橙色,表面呈棕褐色。(图1)。进行了4 mm的穿孔活检,组织学检查显示非泡沫性单核组织细胞弥漫性浸润,乳头真皮内有散布的嗜酸性粒细胞,Touton细胞数量稀少。免疫组织化学对组织细胞标记物CD68呈阳性,而对CD1a和S-100蛋白则呈阴性,表明非朗格汉斯细胞起源。在此基础上,我们确认了巨大的先天性少年黄肉芽肿瘤(JXG)的临床怀疑。

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