Abreu Velez Ana Maria, Dejoseph Louis M, Howard Michael S
Georgia Dermatopathology Associates, Atlanta, Georgia, USA.
N Am J Med Sci. 2011 Oct;3(10):475-7. doi: 10.4297/najms.2011.3475.
Tattoos are produced by introducing colorants of various compositions into the skin, either accidentally or for cosmetic purposes.
A 62-year-old male presented with a cosmetic tattoo and requested a total excision of the lesion. Dermatopathologic analysis of the excised tissue with hematoxylin and eosin examination, as well as immunohistochemistry was performed. H&E staining demonstrated classic histologic features of a tattoo. Utilizing immunohistochemistry, dermal histiocytic antigen presenting cells stained with HAM56 and CD68 antibodies; the staining was present surrounding the tattoo pigment.
We identified two macrophage markers (HAM56 and CD68) surrounding dermal tattoo pigment. A minimal dermal inflammatory immune was noted to the tattoo pigment. Moreover, the immune response and/or tolerance to tattoos is not well characterized. We suggest that tattoo materials and techniques could be utilized in therapeutic delivery for diseases such recessive dystrophic epidermolysis bullosa, potentially preventing immune rejection of gene therapy agents.
纹身是通过将各种成分的色素引入皮肤而形成的,可因意外或出于美容目的。
一名62岁男性因美容纹身前来就诊,并要求对病变进行完整切除。对切除组织进行了苏木精和伊红染色检查以及免疫组织化学分析。苏木精-伊红染色显示出纹身的典型组织学特征。利用免疫组织化学方法,真皮组织中的组织细胞抗原呈递细胞用HAM56和CD68抗体染色;染色出现在纹身色素周围。
我们在真皮纹身色素周围鉴定出两种巨噬细胞标志物(HAM56和CD68)。观察到对纹身色素存在轻微的真皮炎症免疫反应。此外,对纹身的免疫反应和/或耐受性尚未得到充分表征。我们建议纹身材料和技术可用于诸如隐性营养不良性大疱性表皮松解症等疾病的治疗给药,有可能防止基因治疗药物的免疫排斥反应。