Kumarasinghe Sujith Prasad Wanniarachchi, Chin Giam Yoke, Kumarasinghe Marian Priyanthi
National Skin Centre, Singapore.
Arch Pathol Lab Med. 2004 Nov;128(11):e149-52. doi: 10.5858/2004-128-e149-CCPOTS.
Clear cell papulosis of the skin is a rare condition; to our knowledge only 12 cases have been reported. Here, we report for the first time a case of clear cell papulosis with cytokeratin 7 expression and provide a comprehensive literature review. A 16-month-old girl presented with 3 hypopigmented lesions in the pubic region that were 3 to 9 mm in diameter; 1 lesion was papular, and the other 2 were macular. A skin biopsy revealed acanthosis with a proliferation of clear cells along the basal and suprabasal layers of the epidermis occurring in small clusters and singly. The cells had round to oval regular nuclei with abundant to moderate lightly eosinophilic to clear cytoplasm and intracytoplasmic mucin. Immunostaining produced positive results for carcinoembryonic antigen, AE1/3, epithelial membrane antigen, cell adhesion molecule 5.2, and cytokeratin 7 and negative results for gross cystic fluid disease protein, S100, and HMB-45. Clear cells of clear cell papulosis are mucin-positive and S100-negative glandular-secretory epithelial cells with histogenetic features of Toker cells of nipple and Paget cells. Immunohistochemical features support an eccrine secretory cell origin because the clear cells are consistently and strongly positive for carcinoembryonic antigen, positive for cell adhesion molecule 5.2, and negative or rarely positive for gross cystic fluid disease protein.
皮肤透明细胞丘疹病是一种罕见病症;据我们所知,仅报告过12例。在此,我们首次报告1例伴有细胞角蛋白7表达的皮肤透明细胞丘疹病病例,并提供全面的文献综述。一名16个月大女童的耻骨区出现3处色素减退性损害,直径为3至9毫米;1处为丘疹样损害,另外2处为斑疹样损害。皮肤活检显示棘层肥厚,表皮基底层和基底层上出现小簇状和单个散在的透明细胞增生。这些细胞具有圆形至椭圆形的规则细胞核,胞质丰富至中等,轻度嗜酸性至透明,并有胞质内黏液。免疫染色癌胚抗原、AE1/3、上皮膜抗原、细胞黏附分子5.2和细胞角蛋白7呈阳性,而巨囊性积液病蛋白、S100和HMB-45呈阴性。皮肤透明细胞丘疹病的透明细胞是黏液阳性且S100阴性的腺分泌上皮细胞,具有乳头托克尔细胞和佩吉特细胞的组织发生学特征。免疫组化特征支持其来源于小汗腺分泌细胞,因为透明细胞癌胚抗原始终呈强阳性,细胞黏附分子5.2呈阳性,巨囊性积液病蛋白呈阴性或极少呈阳性。