Fukunaga M, Endo Y, Ushigome S, Ishikawa E
Department of Pathology, Jikei University School of Medicine, Tokyo, Japan.
Histopathology. 1995 Jul;27(1):35-42. doi: 10.1111/j.1365-2559.1995.tb00288.x.
We performed a clinicopathological immunohistochemical, ultrastructural, and flow cytometric study on six cases of atypical polypoid adenomyoma of the uterus including one with an adenocarcinoma within it. The tumours occurred in nulliparous women aged 22-48 years (average, 33.0 years); three arose in the uterine corpus, and three in the endocervix. Histologically, they were composed of endometrial glands admixed with a stromal component of interlacing bundles of smooth muscle cells. The glands exhibited varying degrees of architectural and cytological atypia. Most of the stromal cells showed strong staining for HHF35, alpha-smooth muscle actin, and vimentin, and some cells contained desmin. Electronmicroscopy, in one case, confirmed the presence of a well-differentiated smooth muscle component. The stromal component may arise as a result of extensive metaplasia of endometrial stromal cells. Uninvolved endometrium showed ciliated cell metaplasia in three patients, and atypical complex hyperplasia in two. One patient had a well-differentiated adenocarcinoma of endometrioid type arising in an endocervical atypical polypoid adenomyoma. All tumours had a diploid DNA content and relatively small S phase fraction (average, 6.23%). The follow-up periods ranged from 4 to 42 months (average, 13.5 months), and all patients were alive and well. Although the histogenesis of atypical polypoid adenomyoma of the uterus remains uncertain, it is suggested that it may arise because of oestrogen-related factors.
我们对6例子宫非典型息肉样腺肌瘤进行了临床病理、免疫组织化学、超微结构及流式细胞术研究,其中1例合并腺癌。肿瘤发生于22 - 48岁(平均33.0岁)未生育女性;3例发生于子宫体,3例发生于子宫颈。组织学上,它们由子宫内膜腺体与平滑肌细胞交织束状的间质成分混合组成。腺体表现出不同程度的结构和细胞异型性。大多数间质细胞对HHF35、α - 平滑肌肌动蛋白和波形蛋白呈强染色,一些细胞含有结蛋白。电镜检查在1例中证实存在分化良好的平滑肌成分。间质成分可能是子宫内膜间质细胞广泛化生的结果。3例患者未受累的子宫内膜显示纤毛细胞化生,2例显示非典型复杂性增生。1例患者在子宫颈非典型息肉样腺肌瘤中发生了高分化子宫内膜样腺癌。所有肿瘤的DNA含量均为二倍体,S期分数相对较小(平均6.23%)。随访时间为4至42个月(平均13.5个月),所有患者均存活且状况良好。虽然子宫非典型息肉样腺肌瘤的组织发生仍不确定,但提示其可能因雌激素相关因素而发生。