Reed W, Oppedal B R, Eeg Larsen T
Department of Pathology, Ullevål Hospital, Oslo, Norway.
Histopathology. 1990 Jun;16(6):583-8. doi: 10.1111/j.1365-2559.1990.tb01163.x.
Thirty-nine lesions, originally diagnosed as Paget's disease (19), superficial spreading melanoma (13) or Bowen's disease (7), were reviewed. Supplementary immunohistochemistry on routine processed tissue, using antibodies to cytokeratins (PKK1 and M717) and to S-100 protein, was carried out. Two of the lesions, originally classified as Bowen's disease and superficial spreading type malignant melanoma respectively, were reclassified as Paget's disease based on the immunohistochemical findings. Both lesions contained pagetoid cells positive with PKK1. The results indicate that immunohistochemistry may sometimes be valuable in establishing the correct diagnosis in such lesions.
对39个最初诊断为佩吉特病(19个)、浅表扩散性黑素瘤(13个)或鲍温病(7个)的病变进行了回顾。使用细胞角蛋白抗体(PKK1和M717)和S-100蛋白抗体,对常规处理的组织进行了补充免疫组织化学检测。最初分别归类为鲍温病和浅表扩散型恶性黑素瘤的2个病变,根据免疫组织化学结果重新归类为佩吉特病。两个病变均含有PKK1阳性的派杰样细胞。结果表明,免疫组织化学在对此类病变做出正确诊断时有时可能具有重要价值。