Orrell J M, Evans A T, Grant A
Department of Pathology, Ninewells Hospital and Medical School, Dundee, U.K.
J Pathol. 1991 Mar;163(3):239-44. doi: 10.1002/path.1711630309.
There is considerable variation in the quoted mean numbers of AgNORS per nucleus for benign melanonaevi and malignant melanomas. This is partly attributable to different approaches to AgNOR counting. This study summarizes our experience in devising an optimal technique for counting AgNORs. We show that it is essential to count intra-nucleolar AgNORs in addition to those lying outside the nucleolus to obtain clear separation of naevi from melanoma. Although this seems an onerous task, we further demonstrate that a maximum of only 30 nuclei need to be counted to obtain a mean AgNOR count per nucleus which is representative of the whole lesion. This compares with the arbitrary figure of 100 nuclei chosen by most workers. Only by optimizing and standardizing all aspects of the AgNOR technique including fixation, staining, and counting will mean AgNOR counts per nucleus become a useful quick, reproducible method which can be applied to lesions which pose diagnostic problems such as borderline melanocytic lesions.
对于良性黑素痣和恶性黑色素瘤,每个细胞核中所引用的平均银染核仁组织区(AgNORS)数量存在相当大的差异。这部分归因于银染核仁组织区计数的不同方法。本研究总结了我们在设计一种最佳银染核仁组织区计数技术方面的经验。我们表明,除了核仁外的银染核仁组织区,对核仁内的银染核仁组织区进行计数对于将痣与黑色素瘤清晰区分开来至关重要。尽管这似乎是一项艰巨的任务,但我们进一步证明,最多只需计数30个细胞核就能获得每个细胞核的平均银染核仁组织区计数,该计数代表整个病变。这与大多数研究人员随意选择的100个细胞核的数字形成对比。只有通过优化和标准化银染核仁组织区技术的各个方面,包括固定、染色和计数,每个细胞核的平均银染核仁组织区计数才能成为一种有用的、快速且可重复的方法,可应用于诸如交界性黑素细胞病变等存在诊断问题的病变。