Pathology Department of San Cecilio University Hospital, Avenida Madrid 11, Granada, Spain.
Int J Gynecol Pathol. 2011 Sep;30(5):492-6. doi: 10.1097/PGP.0b013e318211d586.
Intestinal metaplasia of the endometrium is extremely uncommon with only a single earlier case report. We describe 2 cases of endometrial intestinal metaplasia, one of them involving an endometrial polyp, characterized by the presence of intestinal-type epithelium containing goblet and neuroendocrine cells, which were positive with CK20, CDX2, chromogranin, and villin. In 1 case, there was concomitant intestinal and pyloric metaplasia in the endocervix. Together with the observation of the earlier reported case of endometrial intestinal metaplasia, there was also intestinal metaplasia in the cervix. This suggests a possible association between intestinal metaplasia at different sites in the female genital tract.
子宫内膜肠上皮化生极为罕见,仅有一例先前的病例报告。我们描述了 2 例子宫内膜肠上皮化生,其中 1 例涉及子宫内膜息肉,其特征为存在含有杯状细胞和神经内分泌细胞的肠型上皮,这些细胞对 CK20、CDX2、嗜铬粒蛋白和微管蛋白呈阳性。在 1 例中,宫颈同时存在肠型和幽门型化生。结合先前报道的子宫内膜肠上皮化生病例,宫颈也存在肠上皮化生。这表明女性生殖道不同部位的肠上皮化生之间可能存在关联。