Ferguson A, Sutherland A, MacDonald T T, Allan F
J Clin Pathol. 1977 Nov;30(11):1068-73. doi: 10.1136/jcp.30.11.1068.
A microdissection and measurement technique has been adapted for biopsy of human small intestine. Specimens fixed in alcohol and acetic acid are Schiff stained in bulk. Villi and crypts are then dissected out under a dissecting microscope, placed under a coverslip, examined, measured, and the number of mitoses in individual crypts counted. With this method specimens of normal small intestine have been found to have villi 500 microns to 1100 microns long and crypts 150 microns to 300 microns. These values were double those obtained when measuring sections of the same specimens stained with haematoxylin and eosin. The mean number of mitoses per crypt in normal duodenum and jejunum ranged from 1 to 12 and most of the cells in mitosis were in prophase or telophase. This rapid, sensitive, and inexpensive technique complements the available methods of measuring small intestinal architecture.
一种显微解剖和测量技术已被应用于人体小肠活检。用酒精和乙酸固定的标本整体进行席夫染色。然后在解剖显微镜下解剖出绒毛和隐窝,置于盖玻片下,进行检查、测量,并计算各个隐窝中的有丝分裂数。用这种方法发现,正常小肠标本的绒毛长度为500微米至1100微米,隐窝长度为150微米至300微米。这些数值是用苏木精和伊红染色的相同标本切片测量值的两倍。正常十二指肠和空肠中每个隐窝的有丝分裂平均数为1至12,大多数处于有丝分裂期的细胞处于前期或末期。这种快速、灵敏且廉价的技术补充了现有的小肠结构测量方法。