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一种用于估计CD138染色骨髓芯针活检切片中浆细胞数量的计数策略。

A counting strategy for estimating plasma cell number in CD138-stained bone marrow core biopsy sections.

作者信息

Smith Fred B, Elnawawi Ashraf

机构信息

Department of Pathology, Saint Vincent's Catholic Medical Centers of New York-Manhattan,and Department of Pathology, New York Medical College, Valhalla, New York, USA.

出版信息

Ann Clin Lab Sci. 2008 Spring;38(2):138-42.

Abstract

Plasma cells are readily identified microscopically after immunostaining for the CD138 antigen, and CD138-stained bone marrow core biopsy sections have proved superior to Giemsa-stained aspirate smears and hematoxylineosin (H&E) sections for determining plasma cell percentages in marrow. The CD138-stained plasma cell percentage is generally obtained by visual estimation, after viewing the entire section. We propose an alternative method, in which the microscopist initially views the immunostained section under low- and medium-power magnification, then selects a single high-power field in which the relative concentration of plasma cells appears most representative of the section as a whole, and performs a manual differential count of plasma cells in that field. On 44 CD138-stained core biopsy specimens from patients with plasma cell myeloma, selected area counting provided plasma cell percentage values that were more closely correlated with total section plasma cell area, determined by computerized image cytometry, than were visual estimates. This simple method requires only slightly more time than visual appraisal, does not require extensive training or experience, and appears to provide a more accurate estimate of the plasma cell population within the entire specimen.

摘要

对CD138抗原进行免疫染色后,浆细胞在显微镜下很容易识别,并且已证明,经CD138染色的骨髓核心活检切片在确定骨髓中浆细胞百分比方面优于吉姆萨染色的涂片和苏木精-伊红(H&E)切片。CD138染色的浆细胞百分比通常是在观察整个切片后通过视觉估计获得的。我们提出了一种替代方法,即显微镜检查人员首先在低倍和中倍放大倍数下观察免疫染色切片,然后选择一个高倍视野,其中浆细胞的相对浓度似乎最能代表整个切片,然后在该视野中对浆细胞进行手动分类计数。在44例来自浆细胞骨髓瘤患者的经CD138染色的核心活检标本中,与视觉估计相比,选定区域计数提供的浆细胞百分比值与通过计算机图像细胞术确定的整个切片浆细胞面积的相关性更高。这种简单的方法只比视觉评估多花费一点时间,不需要广泛的培训或经验,并且似乎能更准确地估计整个标本中的浆细胞数量。

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