p53 and Ki‐67 immunoreactivity and nuclear morphometry of ‘carcinoma‐in‐adenoma’ and adenoma of the gall‐bladder

Twenty lntramucosal tumors of ‘carclnomaln‐adenoma’ and 43 ademas (39 pylorlc gland type, 4 Intestinal type) of the gall‐bladder were studied to establish more precise histo‐logical criteria of carcinoma or adenoma In cases of ‘carcinoma In pyforic gland type adenoma’, to compare carcinoma In adenoma with pure, that Is, without adenomatous components, carcinoma, and to confirm the benign nature of spin‐dle cell fd in the adenomas. Ki‐67 and p53 immunostaining and nuclear morphomety were used. Eight pure intramucessl cancers were used as controls. The formalin‐fixed, paraffln+mbedded sections were stained with p53 and Ki‐67 antibodies. Splndle cell foci were observed only In the adenoma area of the pyloric gland type, wlth a frequency of 23% In 39 adenomas, and of 45% in 20 tumors of carclnoma‐lrradenoma. Ki‐67 staining was negative in 129 of 130 spin‐die cell foci examlned, regardless of their size, and positive in only one focus (550 pm in size, Ki‐67 Index 0.2%). All of the spindle cell foci were negative for p53 stain. The Ki‐67 positive index was 36.6 ± 5.6% In the 8 pure carcinomas, and 12.5 ± 1.9% in the cancer areas of 16 tumors with carcinoma‐in‐adenoma, while it was 7.9 ± 1.7% in the adenoma areas of 16 tumors with carcinoma‐in‐adenoma and 4.9 ± 0.5% in the 32 pure pyloric gland adenomas. The p53‐protein over‐expression was found in seven of eight pure intramucosal cancers, and in one of 16 cancer components of carclnoma‐in‐adenoma. However, it was not found in any of 16 adenoma components of carcinoma‐in‐adenoma, and 35 adenomas. Cells of the cancer tissue of carcinoma‐In‐adenoma showed a significantly larger nuclear area and a larger nuclear minor axis than those of the pyloric gland type adenomas, as well as other architectural and cytologic abnormalities differing from the features of adenomas. These results suggest that clustered spindle cells do not indmte a malignant transformation of adenoma cells and that carcinomas in carcinoma‐in‐adenoma are dtfferent from pylorlc gland type adenomas In terms of morphology and proliferative activity. Moreover, the results of the present study indicate that carcinomas In carcinoma‐ln‐adenoma are lower In malignancy than pure carcinomas, and that their genetic abnormaltty may differ from that of pure carcinomas.