Rashid Sameera, Akhtar Mohammed
Laboratory Medicine and Pathology, Hamad Medical Corporation, Doha, QAT.
Cureus. 2021 Jul 3;13(7):e16148. doi: 10.7759/cureus.16148. eCollection 2021 Jul.
Ciliated cell variant of endometrioid adenocarcinoma (CCVEA) is an extremely rare tumor that has been seldom reported in the literature as low-grade endometrioid carcinoma with a favorable prognosis. CCVEA is characterized by neoplastic glands composed predominantly of ciliated cells with relatively little nuclear atypia. Recognition of the ciliated component is the key to the diagnosis of CCVEA but it can lead to diagnostic confusion with tubal metaplasia especially on endometrial biopsies. Herein, we report the case of a 56-year-old woman who presented with post-menopausal vaginal bleeding. Endometrial biopsy revealed extensive atypical complex endometrial hyperplasia composed predominantly of ciliated cells. The patient subsequently had a hysterectomy and bilateral salpingo-oophorectomy that revealed a large adenomyoma, adherent to the right ovary. The adenomyoma was extensively involved by CCVEA with some extension to the endometrial cavity. To the best of our knowledge, this is the first report of CCVEA that appears to arise in an adenomyoma.
子宫内膜样腺癌的纤毛细胞变体(CCVEA)是一种极其罕见的肿瘤,在文献中很少被报道为预后良好的低级别子宫内膜样癌。CCVEA的特征是肿瘤性腺体主要由纤毛细胞组成,核异型性相对较小。识别纤毛成分是诊断CCVEA的关键,但这可能导致与输卵管化生的诊断混淆,尤其是在子宫内膜活检时。在此,我们报告一例56岁出现绝经后阴道出血的女性病例。子宫内膜活检显示广泛的非典型复杂性子宫内膜增生,主要由纤毛细胞组成。该患者随后接受了子宫切除术和双侧输卵管卵巢切除术,结果显示有一个大的腺肌瘤,附着于右侧卵巢。该腺肌瘤广泛被CCVEA累及,并向子宫内膜腔有一定程度的延伸。据我们所知,这是首次报道CCVEA似乎起源于腺肌瘤。