Gong H, Hayashida H, Kitaoka T, Amemiya T
Department of Ophthalmology, Nagasaki University School of Medicine, Japan.
Eur J Ophthalmol. 2001 Jul-Sep;11(3):301-5. doi: 10.1177/112067210101100314.
Primary adenocarcinoma of the lacrimal gland is a rare malignant tumor of the orbit. Up to now, there has been no presentation of its ultrastructural features. The histopathological findings and fine structures of one case of adenocarcinoma of the lacrimal gland are described in the present work.
The patient was a 59-year-old Japanese man with proptosis that had persisted for one month. A tumor was extirpated, and the tissues were prepared for light and electron microscopic examination.
Electron microscopic examination demonstrated that the tumor cells had well-developed microvilli and lumens. These ultrastructure features are similar to those seen in adenocarcinomas at other sites.
These observations suggest that the accurate diagnosis of rare malignant adenocarcinoma depends not only on routine techniques such as light microscopy of hematoxylin-eosin and PAS-diastase stained slides, but also on electron microscopic findings.
泪腺原发性腺癌是一种罕见的眼眶恶性肿瘤。迄今为止,尚未有其超微结构特征的报道。本文描述了1例泪腺腺癌的组织病理学发现和精细结构。
患者为一名59岁的日本男性,眼球突出持续1个月。切除肿瘤后,将组织制备用于光镜和电镜检查。
电镜检查显示肿瘤细胞有发达的微绒毛和管腔。这些超微结构特征与其他部位腺癌所见相似。
这些观察结果表明,罕见的恶性腺癌的准确诊断不仅依赖于苏木精-伊红染色和PAS-淀粉酶染色切片的光镜等常规技术,还依赖于电镜检查结果。