Katsuta Toshiro, Inoue Tooru, Nakagaki Hiroyuki, Takeshita Morishige, Morimoto Ken, Iwaki Toru
Department of Neurosurgery, Clinical Research Institute, National Kyushu Medical Center Hospital, Fukuoka, Japan.
J Neurosurg. 2003 Feb;98(2):404-6. doi: 10.3171/jns.2003.98.2.0404.
The authors present a rare case of pituicytoma. A dynamic magnetic resonance study performed after Gd injection revealed a markedly, homogeneously enhanced, early-phase pituitary lesion in a 32-year-old woman with a 1-year history of amenorrhea. The tumor bled easily during transsphenoidal resection. The lesion consisted of plump spindle cells and lacked Rosenthal fibers and granular bodies, and thus was different from ordinary pilocytic astrocytoma or any other form of this tumor. Although pituicytoma is often confused with pilocytic astrocytoma when it appears in the sellar region, these two kinds of gliomas should be distinguished on the basis of histological differences.
作者报告了一例罕见的垂体细胞瘤病例。在注射钆后进行的动态磁共振研究显示,一名有1年闭经史的32岁女性的垂体早期病变有明显、均匀强化。该肿瘤在经蝶窦切除术中容易出血。病变由饱满的梭形细胞组成,缺乏罗森塔尔纤维和颗粒体,因此不同于普通的毛细胞型星形细胞瘤或该肿瘤的任何其他形式。尽管垂体细胞瘤出现在鞍区时常常与毛细胞型星形细胞瘤相混淆,但这两种胶质瘤应根据组织学差异加以区分。